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13 pages, 1299 KiB  
Article
The Association of Gender in the Management and Prognosis of Vertebral and Sacral Chordoma: A SEER Analysis
by Aladine A. Elsamadicy, Sumaiya Sayeed, Josiah J. Z. Sherman, Paul Serrato, Shaila D. Ghanekar, Sheng-Fu Larry Lo and Daniel M. Sciubba
J. Clin. Med. 2025, 14(5), 1737; https://doi.org/10.3390/jcm14051737 - 4 Mar 2025
Viewed by 165
Abstract
Background/Objectives: Chordomas are rare primary osseous tumors of the spine and skull base that may portend significant morbidity and mortality. Gender disparities in the management and outcomes of spinal and pelvic chordomas have been sparsely studied. This study aimed to examine the effect [...] Read more.
Background/Objectives: Chordomas are rare primary osseous tumors of the spine and skull base that may portend significant morbidity and mortality. Gender disparities in the management and outcomes of spinal and pelvic chordomas have been sparsely studied. This study aimed to examine the effect of gender on the treatment utilization and outcomes in patients with vertebral column and sacrum/pelvis chordomas. Methods: A retrospective cohort study was performed using the 2000 to 2020 Surveillance, Epidemiology, and End Results (SEER) Registry, a U.S. population-based cancer registry database. Patients with histologically confirmed chordoma of the vertebral column or the sacrum/pelvis were identified using ICD-O-3 codes. The study population was divided into gender-based cohorts: male and female. The patient demographics, tumor characteristics, treatment variables, and mortality were assessed. Results: A total of 791 patients were identified and stratified by gender: 485 (61.3%) male and 306 (38.7%) female. The mean tumor size was similar between the cohorts (p = 0.377), as was the tumor location, with most arising from the pelvic bones/sacrum/coccyx (p = 0.953). While the treatment characteristics did not significantly vary, among patients who received both radiotherapy and surgery, neo-adjuvant radiotherapy was utilized at higher frequencies in the male patients (p = 0.011). For vertebral column chordomas, the median (p = 0.230) and five-year survival (p = 0.220) was similar between cohorts, and gender was not a predictor of survival (p = 0.239). Similarly, for pelvic chordomas, the median (p = 0.820) and five-year survival (p = 0.820) was similar between cohorts, and gender was not associated with survival (p = 0.816). Conclusions: Our study suggests that gender may influence treatment utilization but not mortality in patients with chordomas of the spine and sacrum. Full article
(This article belongs to the Section Clinical Neurology)
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<p>Treatment regimen utilized by patients.</p>
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<p>Survival analyses for patients with chordomas of the (<b>a</b>) vertebral column and (<b>b</b>) pelvis.</p>
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<p>Hazard ratios of various factors among patients with chordomas of the (<b>a</b>) vertebral column and (<b>b</b>) pelvis.</p>
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10 pages, 1607 KiB  
Article
Triangular Screw Placement to Treat Dysmorphic Sacral Fragility Fractures in Osteoporotic Bone Results in an Equivalent Stability to Cement-Augmented Sacroiliac Screws—A Biomechanical Cadaver Study
by Isabel Graul, Ivan Marintschev, Antonius Pizanis, Marcel Orth, Mario Kaiser, Tim Pohlemann, Working Group on Pelvic Fractures of The German Trauma Society and Tobias Fritz
J. Clin. Med. 2025, 14(5), 1497; https://doi.org/10.3390/jcm14051497 (registering DOI) - 24 Feb 2025
Viewed by 231
Abstract
Background: Sacroiliac screw fixation in elderly patients with pelvic fractures remains a challenging procedure for stabilization due to impaired bone quality. To improve it, we investigated the biomechanical properties of combined oblique sacroiliac and transiliosacral screw stabilization versus the additional cement augmentation of [...] Read more.
Background: Sacroiliac screw fixation in elderly patients with pelvic fractures remains a challenging procedure for stabilization due to impaired bone quality. To improve it, we investigated the biomechanical properties of combined oblique sacroiliac and transiliosacral screw stabilization versus the additional cement augmentation of this construct in a cadaver model of osteoporotic bone, specifically with respect to the maximal force stability and fracture-site motion in the displacement and rotation of fragments. Methods: Standardized complete sacral fractures with intact posterior ligaments were created in osteoporotic cadaver pelvises and stabilized with a triangle of two oblique sacroiliac screws from each side with an additional transiliosacral screw in S1 (n = 5) and using the same pelvises with additional cement augmentation (n = 5). A short cyclic loading protocol was applied, increasing the axial force up to 125 N. Sacral fracture-site motion in displacement and rotation of the fragments was measured by optical motion tracking. Results: A maximum force of 65N +/− 12.2 N was achieved using the triangular screw stabilization of the sacrum. Cement augmentation did not provide any significant gain in maximum force (70 N +/− 29.2 N). Only low fragment displacement was observed (2.6 +/− 1.5 mm) and fragment rotation (1.3 +/− 1.2°) without increased stability (3.0 +/− 1.5 mm; p = 0.799; 1.7 +/− 0.4°; p = 0.919) following the cement augmentation. Conclusions: Triangular stabilization using two obliques and an additional transiliosacral screw provides sufficient primary stability of the sacrum. Still, the stability achieved seems very low, considering the forces acting in this area. However, additional cement augmentation did not increase the stability of the sacrum. Given its lack of beneficial abilities, it should be used carefully, due to related complications such as cement leakage or nerve irritation. Improving the surgical methods used to stabilize the posterior pelvic ring will be a topic for future research. Full article
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<p>(<b>A</b>) Schematic drawing of the triangular fixation of the sacrum. Two oblique screws in the S1 vertebra and a transiliosacral screw in the S2 vertebra. (<b>B</b>) Schematic drawing of the additional cement augmentation of the oblique screws in the S1 vertebra. Dotted red line represents the fracture-lines.</p>
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<p>Visualization of the biomechanical test setup with supplied fracture and inserted optical markers. Dotted white line represents the fracture-lines. (<b>a</b>) optical marker, (<b>b</b>) holder on the base plate, (<b>c</b>) mounting to the universal testing machine, (<b>d</b>) visible screw head.</p>
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<p>(<b>A</b>) Displacement of the sacral fragments from the central fragment in the different osteosynthesis procedures. (<b>B</b>) Rotation of the sacral fragments in relation to the central fragment in the different osteosynthesis procedures.</p>
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9 pages, 9808 KiB  
Case Report
Extreme Uterine and Rectal Prolapse in a 31-Year-Old Patient: A Case Report
by Marcin Jozwik, Maria Derkaczew, Joanna Wojtkiewicz, Burghard Abendstein and Maciej Jozwik
J. Clin. Med. 2025, 14(5), 1484; https://doi.org/10.3390/jcm14051484 - 23 Feb 2025
Viewed by 279
Abstract
Background: Pelvic organ prolapse (POP) is a common disorder among postmenopausal women but is rare in very young patients. It can affect various compartments of the pelvic floor. In severe forms, vaginal/uterine and rectal prolapse can occur concurrently. Methods: The aim of this [...] Read more.
Background: Pelvic organ prolapse (POP) is a common disorder among postmenopausal women but is rare in very young patients. It can affect various compartments of the pelvic floor. In severe forms, vaginal/uterine and rectal prolapse can occur concurrently. Methods: The aim of this report is to present a rare case of a young patient with an extreme postpartum uterine and rectal prolapse and our stepwise surgical approach to achieve complete repair while preserving the ability to carry future pregnancies. Results: A 31-year-old patient was admitted with extreme postpartum uterine and rectal prolapse. She underwent three separate surgeries to regain full anatomic reconstruction. Initially, laparoscopic lateral suspension (LLS) according to Dubuisson’s technique was performed in 2017. A combined vaginal-laparoscopic repair followed again in 2017 and included extensive posterior vaginal and perineal repair with absorbable mesh (SeraSynth) attached to the sacrouterine ligaments and laparoscopic hysterosacropexy (HySa) with a non-absorbable PVDF DynaMesh-CESA implant. Finally, in 2019, the DynaMesh-CESA implant was replaced with a T-shaped non-absorbable Albis Posterior Mesh for rectal prolapse, fixed bilaterally to the sacral bone at the S3 level. Additionally, the Dubuisson suspension was adjusted using Noé’s pectopexy for the implant’s reattachment to the pectineal ligaments. Conclusions: Severe uterine and rectal prolapse in young patients is rare and demands a tailored approach. Uterus-preserving surgery should be the priority. In the present case, a resorbable posterior mesh failed in rectal prolapse repair, while a combined rectal prolapse repair and hysteropexy with a non-resorbable posterior mesh proved effective. Full article
(This article belongs to the Special Issue Clinical Management of Pelvic Organ Prolapse)
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<p>(<b>A</b>) Despite the first surgery in February 2017, a total uterine prolapse and rectal prolapse were pronounced at the patient’s admission to our institution in November 2017. (<b>B</b>) Partial improvement with a visible rectocele relapse after a vaginal resorbable mesh placement in the posterior compartment combined with a laparoscopic bilateral hysterosacropexy with a non-resorbable DynaMesh-CESA implant (performed November 2017) at a checkup in December 2018. (<b>C</b>) The final outcome: complete improvement after laparoscopic implantation of a non-resorbable mesh in the posterior compartment with fixation of this implant to the cervix and sacral bone, combined with the bilateral correction of the tension of lateral suspension mesh arms (performed in April 2019). Results stable as of December 2024.</p>
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<p>MRI of pelvic organs in sagittal view. (<b>A</b>) Total uterine and rectal prolapse at the time of admission in November 2017. (<b>B</b>) Final outcome after treatment in April 2018. This anatomical picture remains stable as of December 2024.</p>
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<p>Laparoscopic steps of the final (third) surgical procedure (April 2019). (<b>A</b>) Removal of the DynaMesh-CESA implant. (<b>B</b>) Placement of the Albis Posterior Mesh deep into the rectovaginal space. (<b>C</b>) Fixation of the Albis Posterior Mesh to the posterior cervical wall and bilaterally to the sacral bone. (<b>D</b>) Reattachment of the already present Dubuisson’s implant to the pectineal ligaments according to the uterine pectopexy technique described by Noé et al.</p>
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15 pages, 2086 KiB  
Case Report
Salvage Ultrasound-Guided Robot-Assisted Video-Endoscopic Inguinal Lymphadenectomy (RAVEIL) as a Metastasis-Directed Therapy (MDT) in Oligoprogressive Metastatic Castration-Resistant Prostate Cancer (mCRPC): A Case Report and Review of the Literature
by Rafał B. Drobot, Marcin Lipa and Artur A. Antoniewicz
Curr. Oncol. 2025, 32(2), 115; https://doi.org/10.3390/curroncol32020115 - 18 Feb 2025
Viewed by 488
Abstract
Background: Metastatic castration-resistant prostate cancer (mCRPC) remains challenging due to progression despite androgen deprivation therapy (ADT). Current treatments, including androgen receptor-targeted agents, chemotherapy, bone-targeted agents, and PARP inhibitors, extend survival but face challenges, such as resistance, adverse effects, and limited durability. Metastasis-directed [...] Read more.
Background: Metastatic castration-resistant prostate cancer (mCRPC) remains challenging due to progression despite androgen deprivation therapy (ADT). Current treatments, including androgen receptor-targeted agents, chemotherapy, bone-targeted agents, and PARP inhibitors, extend survival but face challenges, such as resistance, adverse effects, and limited durability. Metastasis-directed therapies (MDTs), such as stereotactic ablative radiotherapy (SABR), show promise in oligometastatic disease, but their role in oligoprogressive mCRPC is unclear. Salvage lymphadenectomy is rarely pursued due to invasiveness and limited data. This is the first report of robotic surgery as an MDT in this setting, demonstrating the potential of salvage robot-assisted video-endoscopic inguinal lymphadenectomy (RAVEIL) to manage oligoprogressive mCRPC and delay systemic progression. Methods: A 47-year-old male with metastatic hormone-sensitive prostate cancer (Gleason 10) underwent ADT, docetaxel chemotherapy, and radical retropubic prostatectomy with super-extended pelvic and retroperitoneal lymphadenectomy. Upon progression to oligoprogressive mCRPC, 68Ga-PSMA PET/CT detected a single metastatic inguinal lymph node. Salvage RAVEIL was performed using the da Vinci X™ Surgical System, guided by preoperative ultrasound mapping. Results: Histopathology confirmed metastasis in one of the eight excised lymph nodes. The patient achieved undetectable PSA levels and prolonged biochemical progression-free survival. Minor complications (lymphorrhea, cellulitis) resolved without sequelae. No further progression was observed for over 14 months. Conclusions: This case highlights RAVEIL as a viable MDT option for oligoprogressive mCRPC, potentially extending progression-free intervals while minimizing systemic treatment. Full article
(This article belongs to the Section Genitourinary Oncology)
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<p>Axial contrast-enhanced CT scan demonstrating paraaortic lymphadenopathy (arrow indicating metastases of prostate cancer in lymph nodes).</p>
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<p>Detailed mapping of the targeted anatomy included the identification of key anatomical landmarks, such as the femoral nerve, femoral artery, femoral vein, great saphenous vein, the femoral triangle (sartorius muscle, adductor longus muscle, and inguinal ligament), and four suspicious lymph nodes.</p>
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<p>Intraoperative view of a robot-assisted video-endoscopic inguinal lymphadenectomy (RAVEIL) with the intention of preserving the great saphenous vein (indicated by the yellow arrow).</p>
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<p>Scheme of trocar placement for robot-assisted video-endoscopic inguinal lymphadenectomy (RAVEIL).</p>
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<p>PSA response to sequential treatments over disease course.</p>
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14 pages, 2027 KiB  
Article
Mesenchymal Stem/Stromal Cells (MSCs) from Mouse Pelvic vs. Long Bones Exhibit Disparate Critical Quality Attributes: Implications for Translational Studies
by Siddaraju V. Boregowda, Cori N. Booker, Jacqueline Strivelli and Donald G. Phinney
Cells 2025, 14(4), 274; https://doi.org/10.3390/cells14040274 - 13 Feb 2025
Viewed by 396
Abstract
Mesenchymal stem/stromal cells (MSCs) have been exploited as an experimental cell therapy in a broad array of clinical applications but have underperformed based on results from pre-clinical studies due to gaps in translating pre-clinical findings to human patients. Herein, we isolated mouse MSCs [...] Read more.
Mesenchymal stem/stromal cells (MSCs) have been exploited as an experimental cell therapy in a broad array of clinical applications but have underperformed based on results from pre-clinical studies due to gaps in translating pre-clinical findings to human patients. Herein, we isolated mouse MSCs from pelvic bone marrow (BMP), a preferred source for human MSCs, and compared their growth, differentiation, and immuno-modulatory activity to those derived from long bone marrow (BML), the traditional source of mouse MSCs. We report that BMP-MSCs exhibit significantly enhanced growth kinetics in 5% and 21% oxygen saturation and superior bi-lineage differentiation and hematopoiesis-supporting activity as compared to BML-MSCs. Additionally, we show that TNF upregulates inducible nitric oxide synthase (NOS2) in BML- and BMP- MSCs and augments their immune suppressive activity in cell-based assays, while interferon-gamma (INFG) upregulates indoleamine, 2-3, dioxygenase (IDO1) and enhances the immune suppressive activity of only BMP-MSCs. These results indicate that mouse MSCs sourced from different bone compartments exhibit measurable differences in critical quality attributes, and these differences are comparable to those observed across species. Based on these differences, BMP- MSCs represent a useful resource to model the behavior of human BM-derived MSCs. Full article
(This article belongs to the Section Stem Cells)
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<p>Isolation of MSCs from BM<sup>L</sup> and BM<sup>P</sup><b>.</b> (<b>a</b>,<b>b</b>), Representative pictures of dissected hind limbs with attached pelvic girdle after surrounding muscle tissue was removed (<b>a</b>) and detached femur with connective tissue removed (<b>b</b>); (<b>c</b>,<b>d</b>), representative pictures of pelvic girdle after surrounding muscle tissue was removed (<b>c</b>) and cleaned of attached connective tissue (<b>d</b>); (<b>e</b>,<b>f</b>), purging of bone marrow from the femur (<b>e</b>) and pubic (<b>f</b>) bones; (<b>g</b>,<b>h</b>), Femur (<b>g</b>) and ilium, ischium, and pubis bones (<b>h</b>) purged of bone marrow. Note bones appear opaque; (<b>i</b>), single-cell suspension of BM<sup>L</sup> produced via mechanical dissociation of purged bone marrow plugs using a 28-gauge need. (<b>j</b>), total number of BM<sup>L</sup> and BM<sup>P</sup> cells recovered on a per-mouse basis; (<b>k</b>,<b>l</b>), total number of plastic adherent cells (<b>k</b>), and MSCs (<b>l</b>) recovered pre- and post-depletion, respectively, from BM<sup>L</sup> and BM<sup>P</sup>; (<b>m</b>,<b>n</b>), yield of immuno-depleted MSCs as a percentage of total BM cells (<b>m</b>) and plastic-adherent cells (<b>n</b>). Data are mean ± SD from paired BM isolations (n = 8) and <span class="html-italic">p</span>-values are by two-tailed Student’s <span class="html-italic">t</span> test. ns = not statistically significant.</p>
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<p>Growth characteristics of BM<sup>L</sup>- and BM<sup>P</sup>-MSCs. (<b>a</b>,<b>c</b>,<b>e</b>), Cumulative yield of BM<sup>L</sup>- and BM<sup>P</sup>-MSCs plated at 1000 cells/cm<sup>2</sup> (<b>a</b>), 2500 cells/cm<sup>2</sup> (<b>c</b>), and 5000 cells/cm<sup>2</sup> (<b>e</b>) and cultured in 5% O<sub>2</sub> vs. 21% O<sub>2</sub> for up to four passages (P0-P3); (<b>b</b>), cumulative yields of BM<sup>L</sup>- and BM<sup>P</sup>-MSCs from (<b>a</b>) as a function of passage number; (<b>d</b>), cumulative yields of BM<sup>L</sup>- and BM<sup>P</sup>-MSCs from (<b>c</b>) as a function of passage number; (<b>f</b>), cumulative yields of BM<sup>L</sup>- and BM<sup>P</sup>-MSCs from (<b>e</b>) as a function of passage number. Data are mean ± SD from a single preparation run in triplicate and <span class="html-italic">p</span>-values in (<b>a</b>,<b>c</b>,<b>e</b>) by a two-tailed Student’s <span class="html-italic">t</span> test. # = number.</p>
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<p>Differentiation and hematopoiesis-supporting capability of BM<sup>P</sup>- and BM<sup>L</sup>-MSCs. (<b>a</b>,<b>b</b>), Bar graphs showing stimulus-induced osteogenic (<b>a</b>) and adipogenic (<b>b</b>) differentiation of BM<sup>L</sup>- and BM<sup>P</sup>-MSCs. Representative photos of cell monolayers stained with Alizarin Red S (<b>a</b>) or AdipoRed (<b>b</b>); (<b>c</b>–<b>e</b>), total colonies recovered from BM<sup>P</sup> and BM<sup>L</sup> cells cultured in growth factor-replete (<b>c</b>,<b>d</b>) or -depleted (<b>e</b>) semi-solid media supplemented with BM<sup>P</sup>- or BM<sup>L</sup>-MSC CM. Data are mean ± SD from two biological replicates run in duplicate and <span class="html-italic">p</span>-values by a two-tailed Student’s <span class="html-italic">t</span> test. # = number.</p>
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<p>Effect of cytokines on immune effector expression in BM<sup>P</sup>- and BM<sup>L</sup>-MSCs. (<b>a</b>), qPCR of <span class="html-italic">Ido1/Gapdh</span> mRNA levels in native BM<sup>P</sup>- and BM<sup>L</sup>-MSCs and following treatment with INFG (100 ng/mL) for 24. Data are mean ± SD from biological replicates performed in quadruplicate; (<b>b</b>), qPCR of <span class="html-italic">Ido1/Gapdh</span> mRNA from MSCs in (<b>a</b>) treated with the indicated concentrations of INFG (24 h). Data are mean ± SD from experiments performed in triplicate; (<b>c</b>), immunoblot of cell extracts from BM<sup>P</sup>- and BM<sup>L</sup>-MSCs treated without or with INFG (100 ng/mL) for 24 h. Bar graph showing IDO1/GAPDH band intensity for INFG-treated samples quantified via Adobe Photoshop; (<b>d</b>), qPCR of <span class="html-italic">Ido1/Gapdh</span> mRNA levels in cells from (<b>a</b>) treated with the indicated concentrations of TNF for 24 h. Data are mean ± SD from experiments performed in quadruplicate; (<b>e</b>,<b>f</b>), qPCR of <span class="html-italic">Nos2/Gapdh</span> mRNA levels in cells from (<b>a</b>) treated without or with the indicated concentrations of TNF (<b>e</b>) or INFG (<b>f</b>) for 24 h. Data are mean ± SD of experiments performed in triplicate; (<b>g</b>), immunoblot of cell extracts from BM<sup>P</sup>- and BM<sup>L</sup>-MSC treated without or with the indicated concentrations of TNF and INFG for 24 h. Bar graph showing NOS2/GAPDH band intensity for TNF + INFG-treated samples quantified via Adobe Photoshop; (<b>h</b>,<b>i</b>), qPCR of <span class="html-italic">Il1ra/Gapdh</span> (<b>h</b>) and <span class="html-italic">LepR/Gapdh</span> (<b>i</b>) mRNA levels in native BM<sup>P</sup>- and BM<sup>L</sup>-MSCs (<b>h</b>,<b>i</b>) or after 24 h treatment with 100 ng/mL INFG. For a and i, <span class="html-italic">p</span>-values are by Student’s <span class="html-italic">t</span> test and for b and d–f by one-way ANOVA with Dunnet’s post hoc test for multiple comparisons with * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001 vs. controls.</p>
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<p>Immuno-suppressive activity of BM<sup>P</sup>- and BM<sup>L</sup>-MSCs. (<b>a</b>,<b>b</b>), Bar graphs showing percentage of CD3<sup>+</sup>Ki67<sup>+</sup> splenocytes in unstimulated cultures, after stimulation with anti-CD3/CD28 activator beads, and in the presence of CM from BM<sup>L</sup>-MSCs (<b>a</b>) and BM<sup>P</sup>-MSCs (<b>b</b>) alone or pre-treated for 48 h with TNF(50 ng/mL), INFG (100 ng/mL), or TNF + INFG. Data are mean ± SD of experiments performed in duplicate and <span class="html-italic">p</span>-values by two-way ANOVA with Dunnet post hoc test. ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.005 vs. stimulated; <sup>###</sup> <span class="html-italic">p</span> &lt; 0.005 vs. CM.</p>
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27 pages, 19579 KiB  
Article
Atypical Pelvic Tumors in Children
by Paulina Sobieraj and Monika Bekiesińska-Figatowska
Cancers 2025, 17(4), 619; https://doi.org/10.3390/cancers17040619 - 12 Feb 2025
Viewed by 533
Abstract
Due to the complex anatomy of the pelvis, various tumors may arise in this region. Some of these tumors are well known and have distinctive features that allow them to be identified by magnetic resonance imaging (MRI). These include sacrococcygeal teratoma (SCT), the [...] Read more.
Due to the complex anatomy of the pelvis, various tumors may arise in this region. Some of these tumors are well known and have distinctive features that allow them to be identified by magnetic resonance imaging (MRI). These include sacrococcygeal teratoma (SCT), the most prevalent congenital tumor in children, often diagnosed prenatally and most frequently occurring in this anatomical location, and ovarian teratoma, which in its mature form is the most common ovarian neoplasm in children and adolescents. Additionally, rhabdomyosarcoma (RMS), commonly found in the bladder in both genders and in the prostate in males, and Ewing sarcoma (ES), affecting the flat bones of the pelvis, are relatively common tumors. In this study, selected atypical pelvic tumors in children are presented. Most of them are tumors of the reproductive system, such as cervical cancer, small cell neuroendocrine carcinoma of the ovary, ES/primitive neuroectodermal tumor (PNET) of the ovary, diffuse large B-cell lymphoma (DLBCL) of the ovaries and ovarian Sertoli–Leydig cell tumor (SLCT) with RMS due to DICER1 syndrome. Additionally, tumors originating from the nervous system, including neuroblastoma (NBL) and plexiform neurofibroma (pNF), associated and not associated with neurofibromatosis type 1 (NF1), are discussed. Furthermore, Rosai–Dorfman disease involving the pelvic and inguinal lymph nodes is presented. By reviewing the literature and presenting our cases, we tried to find radiological features of individual tumors that would bring the radiologist closer to the correct diagnosis, ensuring the implementation of appropriate treatment. However, the MR images cannot be considered in isolation. Additional patient data, such as the clinical picture, comorbidities/syndromes, and laboratory test results, are necessary. Full article
(This article belongs to the Section Pediatric Oncology)
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<p>A fetal MRI. A singleton pregnancy, 29th gestational week (GW). A predominantly cystic sacrococcygeal teratoma, mainly located outside the body, a minor part of it in the pelvis, adjacent to the sacrum—type III, according to the classification of the Section of Pediatric Surgery of the American Academy (<b>a</b>–<b>c</b>, arrows). (<b>a</b>–<b>c</b>)—2D/FIESTA.</p>
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<p>An 11-year-old girl with a giant cystic teratoma of the right ovary (<b>a</b>–<b>f</b>). Typical features of the lesion are present—a gravitationally arranged level of keratinoid material, which shows peripheral diffusion restriction (<b>a</b>,<b>e</b>,<b>f</b>, arrows), a Rokitansky nodule that poorly enhances after the administration of contrast agent (<b>d</b>, arrows), and a fatty element in the wall (<b>b</b>,<b>c</b>, arrows). (<b>a</b>)—FSE/T2; (<b>b</b>)—DIXON/T1 InPhase; (<b>c</b>)—DIXON/T1 WATER; (<b>d</b>)—post-contrast LAVA/T1 WATER; (<b>e</b>)—DWI; (<b>f</b>)—ADC map.</p>
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<p>A 1.5-year-old girl with rhabdomyosarcoma of the bladder. Botryoidal masses in the lumen of the urinary bladder (<b>a</b>–<b>c</b>, arrows). FC—foley catheter. (<b>a</b>–<b>c</b>)—FSE/T2; (<b>d</b>)—post-contrast LAVA/T1 WATER.</p>
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<p>A 13-year-old girl with Ewing sarcoma of the right iliac wing with a giant soft tissue tumor on both sides of the bone (<b>a</b>–<b>f</b>). (<b>a</b>,<b>b</b>)—FSE/T2; (<b>c</b>)—STIR; (<b>d</b>)—post-contrast FSE/T1; (<b>e</b>)—DWI; (<b>f</b>)—ADC map.</p>
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<p>The MRI of a patient with small cell carcinoma of the ovary, hypercalcemic type (<b>a</b>–<b>e</b>). (<b>a</b>,<b>b</b>)—FSE/T2; (<b>c</b>)—post-contrast LAVA/T1 WATER; (<b>d</b>)—DWI; (<b>e</b>)—ADC map.</p>
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<p>The MRI of primitive neuroectodermal tumor/extraskeletal Ewing sarcoma of the left ovary in a 10-year-old patient (<b>a</b>–<b>e</b>). (<b>a</b>,<b>b</b>)—FSE/T2; (<b>c</b>)—post-contrast FSE/T1; (<b>d</b>)—DWI; (<b>e</b>)—ADC map (images courtesy of Prof. K. Jonczyk-Potoczna, Poznan University of Medical Sciences).</p>
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<p>The MRI showing diffuse large B-cell lymphoma of both ovaries and peritoneal infiltrates (<b>a</b>–<b>d</b>). Enlarged ovaries touching each other ((<b>a</b>,<b>c</b>), long arrows, asterisks). Ovarian follicles at the periphery of masses ((<b>b</b>), dotted arrows). Peritoneal infiltration (<b>b</b>, short arrows). (<b>a</b>–<b>c</b>)—FSE/T2; (<b>d</b>)—post-contrast LAVA/T1 WATER.</p>
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<p>A Sertoli–Leydig cell tumor of the right ovary with rhabdomyosarcoma elements on MRI (<b>a</b>–<b>f</b>). (<b>a</b>)—FSE/T2; (<b>b</b>)—FIESTA; (<b>c</b>,<b>d</b>)—post-contrast LAVA/T1 WATER; (<b>e</b>)—DWI; (<b>f</b>)—ADC map.</p>
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<p>The CT exam of the primary ovarian angiosarcoma (<b>a</b>–<b>d</b>). Extensive, cystic-solid mass in the pelvis (images courtesy of Dr. M. I. Furmanek, Medical University of Warsaw).</p>
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<p>The MRI of the peritoneal metastases of ovarian angiosarcoma (<b>a</b>–<b>c</b>, arrows). (<b>a</b>)—STIR; (<b>b</b>,<b>c</b>)—FSE/T2 (images courtesy of Dr. M. I. Furmanek, Medical University of Warsaw).</p>
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<p>MRI of cervical cancer in 16-year-old girl (<b>a</b>,<b>b</b>). (<b>a</b>,<b>b</b>)—FSE/T2.</p>
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<p>MRI of pelvic neuroblastoma (<b>a</b>–<b>c</b>,<b>e</b>,<b>f</b>). Small punctate calcification in tumor on CT scan (<b>d</b>, arrow). (<b>a</b>,<b>b</b>)—FSE/T2; (<b>c</b>)—post-contrast FSE/T1 FS; (<b>e</b>)—DWI; (<b>f</b>)—ADC map.</p>
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<p>Pelvic MRI in Case 1 (<b>a</b>–<b>f</b>). In images (<b>d</b>,<b>e</b>), typical signs of neurofibroma are marked with asterisks: (<b>d</b>)—”target sign”; (<b>e</b>)—”reverse target sign”. (<b>a</b>,<b>b</b>,<b>d</b>)—FSE/T2; (<b>c</b>)—STIR; (<b>e</b>)—post-contrast FSE/T1 F; (<b>f</b>)—post-contrast FSE/T1 post-Gd.</p>
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<p>The pelvic MRI in Case 2 (<b>a</b>–<b>c</b>). The asterisks in (<b>b</b>) indicate infiltration of the anterior uterine wall and anterior cervical surface by plexiform neurofibroma. (<b>a</b>–<b>c</b>)—FSE/T2.</p>
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<p>The pelvic MRI in Case 3 (<b>a</b>–<b>d</b>). A thick arrow in (<b>c</b>) marks the largest lesion forming plexiform neurofibroma with a typical “target sign”. Short arrows in (<b>d</b>) indicate the thickened, infiltrated urinary bladder wall. (<b>a</b>,<b>c</b>)—FSE/T2; (<b>b</b>,<b>d</b>)—STIR.</p>
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<p>The inguinal and pelvic lymph nodes in Rosai–Dorfman disease on MRI (<b>b</b>–<b>d</b>, arrows). (<b>a</b>–<b>c</b>)—STIR; (<b>d</b>)—post-contrast LAVA/T1 WATER.</p>
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11 pages, 1624 KiB  
Article
Acetabular Home Run Screw Guidance for Transiliac Fixation in Cup Revision Arthroplasty
by Martin Wessling, Carsten Gebert, Mohamed Marei, Marcel Dudda, Arne Streitbuerger, Mirko Aach, Lee Jeys, Sven Frieler, Daniela Koller and Yannik Hanusrichter
J. Clin. Med. 2025, 14(3), 922; https://doi.org/10.3390/jcm14030922 - 30 Jan 2025
Viewed by 545
Abstract
Background/Objectives: The growing incidence of acetabular revisions has highlighted the importance of achieving reliable fixation to the remaining bone. Proximal transiliac fixation (TIF) of pelvic implants is becoming an increasingly common approach for managing extensive bone defects. This study seeks to provide guidance [...] Read more.
Background/Objectives: The growing incidence of acetabular revisions has highlighted the importance of achieving reliable fixation to the remaining bone. Proximal transiliac fixation (TIF) of pelvic implants is becoming an increasingly common approach for managing extensive bone defects. This study seeks to provide guidance on TIF implantation by analyzing the optimal screw placement in partial pelvic replacements for acetabular defects. Methods: Between 2014 and 2024, a cohort of 96 consecutive patients (65 females and 31 males) who underwent customized partial pelvic replacement (PPR) with transiliac fixation (TIF) were examined. The angle and entry point of the ideal TIF were determined using preoperative three-dimensional planning and compared with potential influencing factors. Results: All PPRs were successfully implanted, with an average TIF length of 77 mm. The mean anteroposterior angle for TIF was 18° medially and 27° dorsally. Conclusions: Analysis of the entry point showed concentration around the second radius and between the eleven o’clock and one o’clock positions. The AP angle is notably affected by gender and height. Considering the precision of human judgment, a recommendation for TIF placement would be 20° medial and 30° dorsal deviation, with the entry point around the twelve o’clock position and the second ring from the center of the cup. Full article
(This article belongs to the Special Issue Arthroplasty: Advances in Surgical Techniques and Patient Outcomes)
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<p>Illustration of the preoperative condition on the left side and the postoperative outcome after PPR with transiliac fixation on the right side. (<b>a</b>) TIFp, (<b>b</b>) TIFs.</p>
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<p>Exemplary illustration of the measured angles and entry point. (<b>a</b>) The AP angle, which reflects the lateral deviation from the midline in anterior view of the pelvis. (<b>b</b>) The lateral angle of the transiliac fixation in lateral view of the pelvis. (<b>c</b>) The entry point of the screw in the surgeon’s view, in this case 112.</p>
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<p>(<b>a</b>) A plot illustrating a clock face, with the statistically detected entry pointsall examined TIFs. (<b>b</b>) a 3D anatomical rendering of the pelvic bone, demonstrating the spatial distribution of the entry points.</p>
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<p>Boxplot plots illustrating the distribution of the AP angle (<b>a</b>) and lateral angle (<b>b</b>) by gender. The red plots represent female participants, while the green plots represent male participants.</p>
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13 pages, 9413 KiB  
Article
Deep Circumflex Iliac Artery (DCIA) Free-Flap Mandibular Reconstruction Using Patient-Specific Surgical Guides and Customized Plates: A Preliminary Study
by Hyo-Joon Kim, Ji-Su Oh and Seong-Yong Moon
Appl. Sci. 2025, 15(3), 1010; https://doi.org/10.3390/app15031010 - 21 Jan 2025
Viewed by 470
Abstract
Background: Mandibular reconstruction remains challenging in oral and maxillofacial surgery due to its complex anatomy and functional requirements. While Deep Circumflex Iliac Artery (DCIA) flaps offer advantages in bone height and natural contour, their application with computer-aided surgical planning remains limited. Aim: [...] Read more.
Background: Mandibular reconstruction remains challenging in oral and maxillofacial surgery due to its complex anatomy and functional requirements. While Deep Circumflex Iliac Artery (DCIA) flaps offer advantages in bone height and natural contour, their application with computer-aided surgical planning remains limited. Aim: This preliminary study aimed to evaluate the accuracy and clinical outcomes of mandibular reconstruction using DCIA free flaps with patient-specific surgical guides and customized plates. Materials and Methods: A pilot study of five patients who underwent mandibular reconstruction using DCIA free flaps was conducted. Virtual surgical planning was performed using Cone-Beam Computed Tomography (CBCT) and pelvic Computed Tomography (CT) data to design patient-specific cutting guides and reconstruction plates. All surgeries were performed by a single experienced surgeon using standardized techniques. Results: The mean deviation between the virtual planning and actual surgical outcomes was 0.73 ± 0.23 mm, with maximum deviations ranging from 3.87 to 7.83 mm. All flaps achieved 100% survival, with one case (20%) experiencing screw loosening that required plate removal. This complication led to the modification of the plate design to include six or more holes in subsequent cases. Conclusions: Despite limitations including the small sample size and short follow-up period, our preliminary results demonstrate that computer-aided surgical planning with patient-specific devices can significantly improve the accuracy and predictability of DCIA flap mandibular reconstruction, even in challenging revision cases. Further studies with larger patient cohorts are needed to validate these findings. Full article
(This article belongs to the Special Issue Novel Technologies in Oral and Maxillofacial Surgery)
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<p>Preoperative panoramic radiograph.</p>
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<p>Mandible registration for preoperative planning: (<b>a</b>) segmented preoperative mandible; (<b>b</b>) alignment of the position of the mandibular segment using the initial lesion model.</p>
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<p>Virtual surgical planning (VSP): (<b>a</b>) alignment of the iliac crestal bone in the mandibular defect; (<b>b</b>) design of customized plates.</p>
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<p>3D-printed customized plates: (<b>a</b>) plate for distal segment; (<b>b</b>) plate for mesial segment.</p>
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<p>Intraoperative photo: (<b>a</b>) application of iliac bone guide; (<b>b</b>) mandible reconstruction with customized plate; (<b>c</b>) donor site reconstruction with titanium mesh and allobone chip graft (ReadiGRAFT Cancellous Chips; LifeNet Health, Virginia Beach, VA, USA); (<b>d</b>) application of fibrin glue (Greenplast; Green Cross, Yongin, Republic of Korea) after suturing using the internal oblique muscle flap.</p>
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<p>Post-OP analysis: (<b>a</b>) segmented post-OP mandible; (<b>b</b>) accuracy results of VSP compared to actual surgical outcomes.</p>
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<p>(<b>a</b>) Panoramic radiograph 6 months postoperatively; (<b>b</b>) clinical photograph 6 months after surgery with complete epithelialization of the internal oblique muscle flap.</p>
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<p>Modified patient-specific customized reconstruction plate (Case 5).</p>
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11 pages, 2045 KiB  
Article
Radiographic and Clinical Results of Combined Bone and Soft-Tissue Tailored Surgeries for Hip Dislocation and Subluxation in Cerebral Palsy
by Giulia Beltrame, Artemisia Panou, Andrea Peccati, Haridimos Tsibidakis, Francesco Pelillo and Nicola Marcello Portinaro
Children 2025, 12(1), 91; https://doi.org/10.3390/children12010091 - 15 Jan 2025
Viewed by 571
Abstract
Background/Objectives: The aim of the study is to present middle-term results of tailored bone and soft-tissue surgeries in subluxated and dislocated hips in children affected by cerebral palsy. Methods: A total of 87 medical records belonging to 73 children affected by CP, treated [...] Read more.
Background/Objectives: The aim of the study is to present middle-term results of tailored bone and soft-tissue surgeries in subluxated and dislocated hips in children affected by cerebral palsy. Methods: A total of 87 medical records belonging to 73 children affected by CP, treated with combined soft-tissue releases, VDO, and pelvic osteotomy, were reviewed retrospectively. Radiological measurements of AI, RI, and NSA were obtained before surgery, postoperatively, at 12 and 24 months after surgery. Results were assessed globally and by GMFCS, age, and Robin score. Results: Postoperative results are not statistically influenced by age and GMFCS levels at surgery. All three radiographic parameters showed persistent statistically significant improvement after surgery and at follow-up, respectively. Conclusions: Obtaining the best possible concentric reduction of the femoral head in the acetabulum, with simultaneous multilevel soft-tissue rebalancing, creates the best mechanical and biological environment to allow the reshaping of both articular surfaces, obtaining physiological internal joint pressure. The anatomical best congruency is protective from recurrence. Full article
(This article belongs to the Section Pediatric Orthopedics & Sports Medicine)
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<p>(<b>Top right</b>): bilateral femoral head and acetabular dysplasia in a 9-year-old boy GMFCS 4-pre-op; (<b>middle top</b>): immediate post-op of the left hip; (<b>top left</b>): immediate post-op of the right hip, three months apart from the left-sided surgery; (<b>bottom right</b>): follow-up at 12 months; (<b>middle bottom</b>) and (<b>left bottom</b>): post-op at 24 months. Note the good remodeling of the left femoral head.</p>
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<p>Acetabular index pre-operative, postoperative, at 12 months follow-up, and at 24 months follow-up.</p>
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<p>Reimer index pre-operative, postoperative, at 12 months follow-up, and at 24 months follow-up.</p>
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<p>Neck–shaft angle pre-operative, postoperative, at 12 months follow-up, and at 24 months follow-up.</p>
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26 pages, 17112 KiB  
Article
Morphological, Morphometrical and Radiological Features of the Pelvic Limb Skeleton in African Green Monkeys (Chlorocebus sabaeus) from Saint Kitts and Nevis Islands
by Cristian Olimpiu Martonos, Alexandru Ion Gudea, Gilda Rawlins, Florin Gheorghe Stan, Calin Lațiu and Cristian Constantin Dezdrobitu
Animals 2025, 15(2), 209; https://doi.org/10.3390/ani15020209 - 14 Jan 2025
Viewed by 657
Abstract
The paper presents a detailed gross anatomical description of the elements of the pelvic limb in the African green monkey and provides comparative and differential elements on pelvic limb monkey osteology. The osteometric investigation adds value to the gross morphological and radiological investigation, [...] Read more.
The paper presents a detailed gross anatomical description of the elements of the pelvic limb in the African green monkey and provides comparative and differential elements on pelvic limb monkey osteology. The osteometric investigation adds value to the gross morphological and radiological investigation, adjoining metric data to the gross descriptive data set. The main methodology used was the gross morphological investigation, doubled by regular osteometrical and radiographical assessments. For each of the elements, several morphological aspects are described, pointing to the specific and differential aspects that might serve as landmarks in the specific diagnosis of different adaptative changes, related to the type of locomotion. For the pelvis, the aspect of the symphysis, the overall shape of the pelvic inlet, the iliac wing aspect and the acetabular shape are listed as significant elements. The femur has a spherical head with an inferior position of the femoral fovea and a well-developed (tall) greater trochanter, lacking the third trochanter. The medial condyle of the femur is better developed than the lateral one and an evident extensor’s fossa is noted at the level of the distal shaft. The proximal lateral condyloid surface in the tibia is slightly larger than the medial one, with noticeable intercondilar eminences. The fibula is long and unfused with the tibia. Some specific anatomical features are listed only for the talus and calcaneus from tarsals. The study revealed the presence of the gastrocnemius sesamoid bones and the proximal sesamoidi bones as well. Investigation presents a series of osteometrical data with an attempt to show some basic metrical differences among the investigated specimens. Full article
(This article belongs to the Section Mammals)
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<p>Anatomical features of the ilium and acetabulum (<b>A</b>). Acetabulum; (<b>B</b>). Iliac wing—lateral surface; (<b>C</b>). Iliac wing-medial surface. 1. Ilium; 2. Ischium; 3. Pubis; 4. Lunate surface; 5. Acetabular notch; 6. Acetabularossa; 7. Greater ischiatic notch; 8. Ischiatic spine; 9. Tendinous groove; 10. Lesser ischiatic notch; 11. Lateral area of the rectus femoris muscle; 12. Obturator groove; 13. Acetabular margin; 14. Gluteal fossa; 15. Sacral tuberosity of ilium; 16. Crest of ilium; 17. Coxal tuberosity; 18. Dorsal iliac spine; 19. Ventral iliac spine; 19′. Outer lip of the ventral iliac spine; 19″. Inner lip of the ventral iliac spine; 20. Auricular surface; 21. Iliac tuberosity; 22. Iliac fossa.</p>
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<p>Anatomical features of the coxae bones (<b>A</b>). Ventral view; (<b>B</b>). Dorsal view. 1. Ilium; 2. Ischium; 3. Pubis; 4. Wing of ilium; 5. Body of ilium; 6. Lateral area of the rectus femoris muscle; 7. Gluteal fossa; 8. Sacraltuberosity; 9. Dorsal iliac spine; 10. Auricular surfaces; 11. Arcuate line; 12. Psoas minor tuberosity; 13. Greater ischiatic notch; 14. Ischiatic spine; 15. Acetabular margin; 16. Facies lunata; 17. Acetabular notch; 18. Lesser ischiatic notch; 19. Tendinous groove; 20. Ischial tuberosity; 21. Ischial body; 22. Ramus of ischium; 23. Ischial arch; 24. Iliopubic eminence; 25. Pecten pubis; 26. Pubic tubercle; 27. Pelvic symphyses; 27′. Pubic symphysis; 27″. Ischial symphysis; 28. Obturator foramen.</p>
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<p>Coxae bones radiograph (<b>A</b>). Lateral–lateral projection; (<b>B</b>). Ventrodorsal projection. 1. Iliac crest; 2. Sacraltuberosity; 3. Coxal tuberosity; 4. Wing of the ilium; 5. Body of the ilium; 6. Greater ischiatic notch; 7. Ischiatic spine; 8. Lesser ischiatic notch; 9. Ischiatic tuberosity; 10. Femoral head; 11. Greater trochanter; 12. Obturator foramen; 13. Pelvic symphysis; 14. Lesser trochanter; 15. Ilium; 16. Femoral neck; 17. Ischium; 18. Femoral shaft. V-shape dotted lines-the ischiatic arch.</p>
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<p>Pelvic girdle radiograph-ventrodorsal projection. 1. Ilium; 2. Ischium; 3. Pubis; 4. Foramen ovale; 5. Femoral head; 6. Greater trochanter; 7. Lesser trochanter; 8. Trochanteric fossa; 9. Intertrochanteric crest; 10. Femoral shaft; 11. Ischiatic arch. Blue dotted line-the acetabulum; White dotted line-the femoral neck.</p>
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<p>Anatomical features of the femur. Cranial aspect (<b>A</b>),Caudal aspect (<b>B</b>), Details of the medial part of proximal extremity (<b>C</b>), Details of the cranial part of distal extremity (<b>D</b>), Details of the caudal part of proximal extremity(<b>E</b>), Femur- details of the caudal part of distal extremity (<b>F</b>) 1. Femoral shaft; 2. Femoral head; 3. Fovea for ligament of head of femur; 4. Neck of femur; 5. Greater trochanter; 6. Lesser trochanter; 7. Intertrochanteric crest; 8. Trochanteric fossa; 9. Intertrochanteric line; 10. Gluteal tuberosity; 11. Linea aspera; 12. Pectineal line of femur; 13. Lateral trochlear lip; 14. Medial trochlear lip; 15. Lateral epicondyle; 16. Medial epicondyle; 17. Medial femoral condyle; 18. Lateral femoral condyle; 19. Medial supracondylar line; 20. Lateral supracondylar line; 21. Articular surface for the medial gastrocnemius sesamoid bone; 22. Articular surface for the lateralsesamoid bone of gastrocnemius; 23. Vascular foramina; Black asterix—Intercondylar fossa; White arrowheads—intercondylar line; Red asterix—popliteal fossa. Dotted circle (<b>D</b>)—ligamentary fossa.</p>
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<p>Stifle joint radiograph—medio-lateral projection. 1. Femur; 2. Femoral trochlea; 3. Patella; 4. Sesamoid bone of gastrocnemius; 5. Patellar ligament; 6. Femoral condyle; 7. Intercondylar tuberosity; 8. Medial condyle of the tibia; 9. Tibial tuberosity; 10. Proximal tibio-fibilar joint; 11. Tibial tuberosity; 12. Head of fibula; 13. Body of fibula.</p>
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<p>Anatomical features of the patella (<b>A</b>). Cranial surface; (<b>B</b>). Articular surface. 1. Patella; 2. Base of patella; 3. Medial margin of the patella; 4. Lateral margin of the patella; 5. Medial patellar tuberosity; 6. Apex of the patella.</p>
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<p>Anatomical features of the tibia and fibula bones (<b>A</b>). Fibula (lateral-left and medial-right); (<b>B</b>). Tibia caudal view; (<b>C</b>). Tibia cranial view; (<b>D</b>). Tibia lateral view; (<b>E</b>,<b>F</b>). Proximal end of tibia. 1. Body of tibia; 2. Body of fibula; 3. Head of fibula; 4. Articular surface of head of fibula; 5. Lateral malleolus; 6. Lateral tibial condyle; 7. Medial tibial condyle; 8. Intercondylar eminence; 8′. Medial intercondylar tubercle; 8″. Lateral intercondylar tubercle; 9. Popliteal notch; 10. Fibular notch; 11. Medial malleolus; 12. Tibial tuberosity; 13. Extensor’s groove; 14. Distal fibular articular surface; 15. Tibial cochlea; 16. Tibial tuberosity; 17. Medial condyle; 18. Lateral condyle; 19. Cranial intercondylar area; 20. Caudal intercondylar area.</p>
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<p>Anatomical features of the pes region (<b>A</b>). Tarsal bones—dorsal view; (<b>B</b>). Digital area—dorsal view; (<b>C</b>). Third digit skeleton—dorsal view. 1. Talus; 2. Calcaneus; 3. Central tarsal bone; 4. First tarsal bone; 5. Second tarsal bone; 6. Third tarsal bone; 7. Fourth tarsal bone; 8. First metatarsal bone; 9. Second metatarsal bone; 10. Third metatarsal bone; 11. Fourth metatarsal bone; 12. Fifth metatarsal bone; 13. Articular surface for distal tarsal bone; 14. Base of metatarsal bone; 15. Body of metatarsal bone; 16. Head of metatarsal bone; a. First phalanges of digits I–V; b. Second phalanges of digits II–V; c. Third phalanges of digits I–V.</p>
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<p>Anatomical features of the calcaneus and talus bones (<b>A</b>). Calcaneus-plantar view; (<b>B</b>). Calcaneus—dorsal view; (<b>C</b>). Talus—dorsal view; (<b>D</b>). Talus—plantar view. 1. Calcaneus; 2. Calcaneal tuberosity; 2′. Lateral calcaneal process; 2″. Medial calcaneal process; 3. Sustentaculum tali; 4. Tendinous groove; 5. Peroneal tubercle; 6. Calcaneal tubercle; 7. Proximal talar articular surface; 8. Middle talar articular surface; 9. Calcaneal sulcus; 10. Distal talar articular surface; 11. Articular surface for the fourth tarsal bone; 12. Talus; 13. Body of the talus; 14. Neck of the talus; 15. Head of the talus; 16. Trochlea of the talus; 17. Lateral tubercle; 18. Medial talar articular surface; 19. Medial tubercle; 20. Proximal talar articular surface; 21. Talar sulcus; 22. Lateral talar articular surface; 23. Distal talar articular surface; 24. Articular surface for the central tarsal bone.</p>
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<p>Pes area-radiograph dorso-plantar projection. 1. Tibia; 2. Fibula; 3. Medial malleolus; 4. Lateral malleolus; 5. Peroneal tubercle; 6. Calcaneus; 7. Talus; 8. Fourth tarsal bone; 9. Central tarsal bone; 10. Third tarsal bone; 11. Second tarsal bone; 12. First tarsal bone; 13. Metatarsal bone I–V; 14. Metacarpophalangeal joint of digit I; Proximal phalanx of digit I; 16. Proximal sesamoids; 17. Distal phalanx of digit I; 18. Proximal phalanges of digits II–V; 19. Middle phalanges of digits II–V; 20. Distal phalanges of digits II–V; 21. Distal sesamoid of digit I, Asterix—tibiofibular interosseous space.</p>
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19 pages, 6070 KiB  
Article
A Prospective Observational Cohort Study Comparing High-Complexity Against Conventional Pelvic Exenteration Surgery
by Charles T. West, Abhinav Tiwari, Yousif Salem, Michal Woyton, Natasha Alford, Shatabdi Roy, Samantha Russell, Ines S. Ribeiro, Julian Smith, Hideaki Yano, Keith Cooper, Malcolm A. West and Alex H. Mirnezami
Cancers 2025, 17(1), 111; https://doi.org/10.3390/cancers17010111 - 1 Jan 2025
Viewed by 1038
Abstract
Background: Conventional pelvic exenteration (PE) comprises the removal of all or most central pelvic organs and is established in clinical practise. Previously, tumours involving bone or lateral sidewall structures were deemed inoperable due to associated morbidity, mortality, and poor oncological outcomes. Recently however [...] Read more.
Background: Conventional pelvic exenteration (PE) comprises the removal of all or most central pelvic organs and is established in clinical practise. Previously, tumours involving bone or lateral sidewall structures were deemed inoperable due to associated morbidity, mortality, and poor oncological outcomes. Recently however high-complexity PE is increasingly described and is defined as encompassing conventional PE with the additional resection of bone or pelvic sidewall structures. This observational cohort study aimed to assess surgical outcomes, health-related quality of life (HrQoL), decision regret, and costs of high-complexity PE for more advanced tumours not treatable with conventional PE. Methods: High-complexity PE data were retrieved from a prospectively maintained quaternary database. The primary outcome was overall survival. Secondary outcomes were perioperative mortality, disease control, major morbidity, HrQoL, and health resource use. For cost–utility analysis, a no-PE group was extrapolated from the literature. Results: In total, 319 cases were included, with 64 conventional and 255 high-complexity PE, and the overall survival was equivalent, with medians of 10.5 and 9.8 years (p = 0.52), respectively. Local control (p = 0.30); 90-day mortality (0.0% vs. 1.2%, p = 1.00); R0-resection rate (87% vs. 83%, p = 0.08); 12-month HrQoL (p = 0.51); and decision regret (p = 0.90) were comparable. High-complexity PE significantly increased overall major morbidity (16% vs. 31%, p = 0.02); and perioperative costs (GBP 37,271 vs. GBP 45,733, p < 0.001). When modelled against no surgery, both groups appeared cost-effective with incremental cost-effectiveness ratios of GBP 2446 and GBP 5061. Conclusions: High-complexity PE is safe and feasible, offering comparable survival outcomes and HrQoL to conventional PE, but with greater morbidity and resource use. Despite this, it appears cost-effective when compared to no surgery and palliation. Full article
(This article belongs to the Special Issue Perioperative and Surgical Management of Gastrointestinal Cancers)
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<p>Intra-operative photos of high-complexity pelvic exenteration (PE): (<b>A</b>) Prone view of high-sacrectomy (HS) with arrow at level of division. (<b>B</b>) Complete sidewall resection exposing sciatic nerve (SN) with forceps indicating cut end of ischial spine. (<b>C</b>) Resection and reconstruction of common iliac artery (CIA) and common iliac vein (CIV) with bovine pericardium tube grafts.</p>
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<p>Kaplan–Meier survival plots, log-rank tests, and risk tables comparing conventional pelvic exenteration (PE) in red to high-complexity PE in blue: (<b>a</b>) overall survival, (<b>b</b>) disease-free survival, and (<b>c</b>) local-disease-free survival including only pelvic recurrences. Note: Five patients with benign disease were excluded from disease-free survival analyses.</p>
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<p>Kaplan–Meier survival plots, log-rank tests, and risk tables comparing conventional pelvic exenteration (PE) in red to high-complexity PE in blue: (<b>a</b>) overall survival, (<b>b</b>) disease-free survival, and (<b>c</b>) local-disease-free survival including only pelvic recurrences. Note: Five patients with benign disease were excluded from disease-free survival analyses.</p>
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<p>Trajectories of EQ5D-5L utility scores and decision regret scale (DRS) scores over time for conventional pelvic exenteration (PE) in blue against high-complexity PE in red; EQ5D-5L score lines are continuous and DRS scores are dashed. Individual points on scatterplot were removed and regression lines drawn with locally estimated scatterplot smoothing; left y-axis shows EQ5D-5L utility scores ranging from 0.00 to 1.00, with 0.00 representing death and 1.00 indicating excellent quality of life. Right y-axis shows DRS scores ranging from 0 to 100, with 0 representing no decisional regret, and 100 indicating maximal decisional regret. Dropout rates described in <a href="#app1-cancers-17-00111" class="html-app">Table S2</a>.</p>
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18 pages, 5368 KiB  
Article
The Musculoskeletal Anatomy of the Komodo Dragon’s Hindlimb (Varanus komodoensis, Varanidae)
by Anna Tomańska, Martyna Stawinoga, Tomasz Gębarowski, Maciej Janeczek, Joanna Klećkowska-Nawrot, Karolina Goździewska-Harłajczuk and Maciej Dobrzyński
Animals 2025, 15(1), 35; https://doi.org/10.3390/ani15010035 - 26 Dec 2024
Viewed by 981
Abstract
The Komodo dragon (Varanus komodoensis) is the largest extant lizard and is classified as an endangered species. Despite its rarity, anatomical studies on this species remain limited, hindering a comprehensive understanding of its biology and evolutionary traits. This research presents a [...] Read more.
The Komodo dragon (Varanus komodoensis) is the largest extant lizard and is classified as an endangered species. Despite its rarity, anatomical studies on this species remain limited, hindering a comprehensive understanding of its biology and evolutionary traits. This research presents a detailed anatomical and histological examination of the pelvic limb of a female Komodo dragon, providing valuable insights into the musculoskeletal system of this species. A series of measurements and observations were made on the bones of the pelvic limb, including the femur, tibia, fibula, and pes, all of which are essential for supporting the animal’s large body size and facilitating its predatory behavior. This study also highlights the diverse muscle architecture, where large muscle masses are associated with the femoral retractors and ankle plantarflexors. Histological analysis of the muscle fibers revealed significant variability in fiber diameters, supporting the functional adaptation of the Komodo dragon’s limbs for high-speed ambush predation. This research provides important morphological data that could inform clinical practices, including orthopedic procedures and physiotherapy for Komodo dragons in zoological settings. Additionally, these findings shed light on the evolutionary patterns inherited from the species’ ancestors, which contributed to the development of its distinctive biological adaptations. Full article
(This article belongs to the Section Veterinary Clinical Studies)
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<p>Skin of the sole of the Komodo dragon’s pes. (<b>A</b>). Cross-sectional view of the skin emphasizing the horny epidermal scales (squamae epidermales cornificatae). The histological image was stained with hematoxylin and eosin (HE). (<b>A.1</b>)—a cross-section of the skin with annotated stratum corneum, epidermis, and dermis (corium), Mag 100×. (<b>A.2</b>)—a longitudinal section of the skin with annotations for periderm (peridermis), horny epidermal scales (squamae epidermales cornificatae), stratum corneum, stratum Malpighii, and loose connective tissue (textus connectivus laxus), Mag 200×.</p>
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<p>The posterio-anterior (<b>A</b>) and lateral (<b>B</b>) view of the right pelvic limb of the Komodo dragon (X-rays). The following anatomical structures are visible: femur with its internal trochanter and shaft; condyles and intercondylar groove; tibia with its distal extremity; calcaneum; fibula with the distal epiphysis of the fibula; astragalus with intermedium and central tarsal bone; distal tarsal III; metatarsal V; metatarsal I; I—digit I; II—digit II; III—digit III; IV—digit IV; and V—digit V.</p>
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<p>The skeletal structure of the right pelvic limb of the Komodo dragon, emphasizing its connection to the pelvis. It includes the pelvis, femur, tibia, fibula, metatarsals, calcaneum bone, and digits. Labels: I—digit I; II—digit II; III—digit III; IV—digit IV; and V—digit V. The illustration is based on the anatomical examination and photographic documentation of the comparative specimen from the collections of the Nature Museum at the Faculty of Biology and Animal Science, Wrocław University of Environmental and Life Sciences (Wrocław, Poland) [<a href="#B21-animals-15-00035" class="html-bibr">21</a>]. Created by A. Tomańska.</p>
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<p>Muscular anatomy of the right pelvic limb, including the following muscles: pubotibial muscle (<span class="html-italic">m. pubotibialis</span>), tibialis anterior muscle (<span class="html-italic">m. tibialis anterior</span>), femoral adductor muscle (<span class="html-italic">m. adductor femoralis</span>), ambiens muscle (<span class="html-italic">m. ambiens</span>) external flexor of the tibia muscle (<span class="html-italic">m. flexor tibialis externus</span>), gastrocnemius muscle (<span class="html-italic">m. gastrocnemius</span>), extensor digitorum longus muscle (<span class="html-italic">m. extensor digitorum longus</span>), fibularis longus muscle (<span class="html-italic">m. fibularis longus</span>), fibularis brevis muscle (<span class="html-italic">m. fibularis brevis</span>), flexor digitorum superficialis muscle (<span class="html-italic">m. flexor digitorum superficialis</span>), flexor digitorum longus muscle (<span class="html-italic">m. flexor digitorum longus</span>), and pronator quadratus muscle (<span class="html-italic">m. pronator quadratus</span>). Labels: I—digit I; II—digit II; III—digit III; IV—digit IV; and V—digit V. The figure on the left illustrates the proximal part of the limb, located closer to the body axis. The central illustration depicts the dorsal aspect of the limb, including the dorsal surface of the pes (<span class="html-italic">dorsum pedis</span>). The figure on the right presents the limb in lateral view (<span class="html-italic">pars lateralis</span>). Images of the pelvic limb are also available in <a href="#app1-animals-15-00035" class="html-app">Supplementary Material</a>. Illustration created by A. Tomańska.</p>
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<p>Histological images of selected pelvic limb muscles (HE staining). (<b>A</b>)—ambiens muscle (<span class="html-italic">m. ambiens</span>, dorsal head), Mag 200×; (<b>B</b>)—puboischiofemoral muscle (<span class="html-italic">m. puboischiofemoralis</span>), Mag 200×; (<b>C</b>)—flexor digitorum longus muscle (<span class="html-italic">m. flexor digitorum longus</span>), Mag 200×; (<b>D</b>)—superficial flexor of the tibia muscle (<span class="html-italic">m. flexor tibialis superficialis</span>), Mag 200×; (<b>E</b>)—femorotibial muscle (<span class="html-italic">m. femorotibialis</span>), Mag 200×; (<b>F</b>)—pubotibial muscle (<span class="html-italic">m. pubotibialis</span>), Mag 200×.</p>
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<p>The distribution of muscle fiber diameters (µm, N = 100), circumference (cm), length (cm), and weight (g) across the various muscles of the pelvic limbs is presented. The data were visualized using Datawrapper and correspond to the information detailed in <a href="#animals-15-00035-t001" class="html-table">Table 1</a>.</p>
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<p>Muscle weight-to-body weight ratios for the pelvic limb musculature of <span class="html-italic">Varanus komodoensis</span> specimen: adductor femoral, 0.089; ambiens (dorsal head), 0.146; iliofibular, 0.117; iliotibial, 0.111; femorotibial, 0.029; extensor digitorum longus, 0.051; anterior tibial, 0.019; flexor digitorum longus, 0.145; superficialis flexor of the tibial, 0.151; internal flexor of the tibial, 0.044; gastrocnemius, 0.064; fibularis brevis, 0.044; fibularis longus, 0.067; anterior ibial, 0.047; puboischiotibial, 0.284; pubotibial (dorsal head), 0.048; and pubotibial (ventral head), 0.044. Visualized using Datawrapper.</p>
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<p>Muscle fiber diameter-to-muscle length ratios in the pelvic limb musculature of the examined <span class="html-italic">Varanus komodoensis</span> specimen: adductor femoris, 3.77; ambiens (dorsal head), 5.14; extensor digitorum longus, 3.90; femorotibial, 4.22; flexor digitorum longus, 4.91; anterior tibial, 3.72; superficial flexor of the tibia, 6.31; internal flexor of the tibia, 7.56; gastrocnemius, 3.43; iliofibular, 3.96; iliotibial, 4.20; fibularis brevis, 3.92; fibularis longus, 3.58; puboischiofemoral, 5.16; puboischiotibial, 6.91; pubotibial (dorsal head), 3.80; pubotibial (ventral head), 6.07; and anterior tibial, 6.36. Visualized using Datawrapper.</p>
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15 pages, 1276 KiB  
Review
Atypical Metastases from Prostate Cancer: Alpha-Methylacyl-Coenzyme A Racemase (AMACR) as a Potential Molecular Target in Prostate-Specific Membrane Antigen-Negative Prostate Adenocarcinoma
by Ilham Badrane, Angelo Castello, Matteo Brunelli, Corrado Cittanti, Sara Adamantiadis, Ilaria Bagni, Noemi Mindicini, Federica Lancia, Massimo Castellani, Licia Uccelli, Mirco Bartolomei and Luca Urso
Biomolecules 2025, 15(1), 17; https://doi.org/10.3390/biom15010017 - 26 Dec 2024
Viewed by 885
Abstract
Prostate cancer (PCa) is a high-prevalence disease usually characterized by metastatic spread to the pelvic lymph nodes and bones and the development of visceral metastases only in the late stages of disease. Positron Emission Tomography (PET) plays a key role in the detection [...] Read more.
Prostate cancer (PCa) is a high-prevalence disease usually characterized by metastatic spread to the pelvic lymph nodes and bones and the development of visceral metastases only in the late stages of disease. Positron Emission Tomography (PET) plays a key role in the detection of PCa metastases. Several PET radiotracers are used in PCa patients according to the stage and pathological features of the disease, in particular 68Ga/18F-prostate-specific membrane antigen (PSMA) ligands. Moreover, 2-deoxy-2-[18F]fluoro-D-glucose 18F-FDG PET usually shows metastases in the late stages of disease, when dedifferentiated neoplastic clones lose PSMA expression. In some cases, PCa patients may present atypical sites of metastases, with uncommon appearance at PET imaging with different radiotracers. We present the case of a patient with biochemical recurrence of PCa (ISUP Grade Group IV; PSA 4.7 ng/mL) showing atypical sites of metastases (the testis and multiple lung nodules) with absent PSMA expression and high [18F]FDG avidity. The patient showed diffuse positivity to alpha-methylacyl-coenzyme A racemase (AMACR). Moreover, a literature review was performed by collecting cases of PCa patients with atypical metastatic spread detected via PET imaging, with the aim of highlighting the relationship between atypical sites of metastases, imaging presentation, and pathology findings. Full article
(This article belongs to the Special Issue Advances in the Pathology of Prostate Cancer)
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<p>The figure shows the maximum intensity projection (MIP) of 2 [<sup>68</sup>Ga]Ga-PSMA-11 PET/CT studies. The first (<b>A</b>) was performed in a patient with BCR of PCa after radical prostatectomy (ISUP Grade Group 3; PSA = 0.63 ng/mL), without evidence of pathological PSMA uptake. The study shows the physiological distribution of PSMA ligand PET, with intense uptake in the salivary and lacrimal glands, spleen, and kidneys and mild radiotracer uptake in the liver and bowel. The second scan (<b>B</b>) demonstrates multiple metastases of PCa (red arrows) in a patient undergoing primary staging of very-high-risk PCa (ISUP Grade Group 5; PSA = 43.69 ng/mL).</p>
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<p>The figure shows axial fused images of [<sup>18</sup>F]FDG (<b>A</b>,<b>B</b>) and [<sup>68</sup>Ga]Ga-PSMA-11 PET/CT (<b>C</b>,<b>D</b>). Of note, the right testicular lesion shows much higher uptake intensity at [<sup>18</sup>F]FDG PET/CT than at [<sup>68</sup>Ga]Ga-PSMA-11 PET/CT. Similarly, the lung lesions are [<sup>18</sup>F]FDG avid and PSMA negative. The case highlights an atypical metastatic pattern, both in terms of atypical localizations (testis and lung metastases) and of multimodal PET imaging positivity ([<sup>18</sup>F]FDG avid and with low/absent PSMA expression).</p>
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<p>Immunohistochemistry of the resected testicular mass. The mass shows intense positivity to AMACR (<b>A</b>), positivity to PCT (<b>B</b>) and PSA (<b>C</b>), and negative expression for PSMA (<b>D</b>).</p>
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<p>[<sup>18</sup>F]F-PSMA-1007 PET/CT images revealed, along with primary PCa (<b>A</b>), a left adrenal lesion (<b>B</b>) in a patient with PCa (ISUP Grade Group = 5) during ADT.</p>
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<p>Maximum intensity projection (MIP) and axial fused [<sup>68</sup>Ga]Ga-PSMA-11 PET/CT images in a patient with cerebral and cerebellar metastases in PCa (ISUP Grade Group = 5).</p>
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8 pages, 4947 KiB  
Case Report
Subcapital Femoral Neck Fracture in a Professionally Active Patient Undergoing Palliative Treatment for Endothelial Cell-Derived Epithelioid Haemangioendothelioma (EHE)
by Paulina Kluszczyk, Aleksandra Tobiasz, Dawid Szumilas, Mateusz Winder, Jacek Pająk, Robert Kwiatkowski and Jerzy Chudek
Reports 2024, 7(4), 111; https://doi.org/10.3390/reports7040111 - 9 Dec 2024
Viewed by 787
Abstract
Background and Clinical Significance: Femoral neck fracture frequently occurs in the elderly population but may also present in patients diagnosed with primary cancer or bone metastases. A pathological, oligosymptomatic fracture associated with epithelioid haemangioendothelioma (EHE), a rare endothelial cell-derived sarcoma, is uncommon. Case [...] Read more.
Background and Clinical Significance: Femoral neck fracture frequently occurs in the elderly population but may also present in patients diagnosed with primary cancer or bone metastases. A pathological, oligosymptomatic fracture associated with epithelioid haemangioendothelioma (EHE), a rare endothelial cell-derived sarcoma, is uncommon. Case Presentation: A 44-year-old patient underwent biopsy procedures three times (2010, 2012, 2013) for a focal lesion of the left ischium, none confirming its malignant nature. The last biopsy revealed a neoplastic tissue with features of discrete dysplasia. The lesion did not undergo medical follow-up for seven consecutive years. In August 2020, the patient presented with right lower limb pain. A CT scan, PET/CT scan, and biopsy confirmed EHE with spindle/sarcomatous features. In November 2020, chemotherapy (5xADIC) started (PET/CT confirmed a partial response). After its completion in July 2021, bone progression occurred and sirolimus-based therapy was started. After 3 months, a small liver metastasis was visualized on PET/CT, which did not result in the termination of treatment. In December 2021, pamidronate-based antiresorptive therapy was started. Liver metastasis remained stable in follow-up CT scans. Due to pelvic and spinal lesions, the patient was assisted by elbow crutches and underwent radiotherapy, remaining professionally active. The patient did not report any trauma, but in August 2023, a subsequent CT scan revealed a subcapital fracture of the left femoral neck in the fusion phase. Due to pelvic changes and the stable nature of the fracture, surgical treatment was abandoned. Conclusions: An oligosymptomatic femoral neck fracture, not requiring medical intervention is considered a rare complication of bone cancer. Full article
(This article belongs to the Section Oncology)
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<p>CT scan from 2009 (<b>A</b>) showing a well-demarcated osteolytic lesion in the left ischium (red arrow). The mean density of the tumour in the pre-contrast scan was 87 Hounsfield units (HU) and showed moderate enhancement in the subsequent phases reaching 112 HU in the venous phase. PET-CT from 2009 (<b>B</b>) with increased radiotracer uptake at the tumour location (red arrow).</p>
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<p>Haematoxylin and eosin (HE) staining (magnification is shown for each picture). (<b>A</b>) Intertrabecular space (a bone trabeculae visible in the lower left corner) filled with malignant mesenchymal neoplastic cells with myxomatous lining. Epithelioid, polymorphic tumour cells. (<b>B</b>) Epithelioid and spindle-shaped tumour cells. (<b>C</b>) Cluster of epithelioid cells. (<b>D</b>) Spindle-shaped tumour cells with intracytoplasmic inclusions. (<b>E</b>) Tumour cells with intracytoplasmic inclusions. (<b>F</b>) Cluster of tumour cells. Erythrocytes are visible in the cytoplasm of one tumour cell (central part of the photo). (<b>G</b>) Cluster of tumour cells. In a single cell, intranuclear inclusion and an eosinophil are visible. (<b>H</b>) Cluster of tumour cells. A lymphocyte visible in the cytoplasm of a single cell. (<b>I</b>) The interbone space filled with malignant mesenchymal neoplasm with myxomatous lining. Polymorphic epithelioid tumour cells.</p>
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<p>CT scans from September 2022 (<b>A</b>), January 2023 (<b>B</b>), and April 2023 showing decreased bone density in the left femur and pathological lesions in the vertebrae and left pelvic bones. Early signs of a subcapital fracture of the left femoral neck (red arrow) first seen in the CT from April 2023 (<b>C</b>).</p>
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<p>CT scan from August 2023 (<b>A</b>) showing extensive lytic infiltration of the left ischium at the initial tumour site (red arrow). Coronal plane maximum intensity projection (MIP) of the same CT (<b>B</b>). Impacted fracture of the left femoral neck (blue arrowhead) caused by the neoplastic infiltration. Pathological lesions in the left ischium and hip bone as well as in ribs 10 and 11 on the right side.</p>
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12 pages, 5342 KiB  
Technical Note
Effectiveness of Virtual Surgical Planning and Three-Dimensional Anatomical Models in Radiological Reconstruction of Center of Rotation and Pelvic Brim in Patients with Anterior Column Defects Requiring Revision Hip Arthroplasty
by Krzysztof Andrzejewski, Marcin Domzalski, Bozena Rokita, Jan Poszepczynski and Piotr Komorowski
Diagnostics 2024, 14(22), 2574; https://doi.org/10.3390/diagnostics14222574 - 15 Nov 2024
Viewed by 547
Abstract
Background: The aim of this study was to show that virtual surgical planning (VSP) and printed anatomical models support the reconstruction of the center of rotation (COR) and pelvic BRIM during revision hip surgery using a dual-mobility revision cup system in patients with [...] Read more.
Background: The aim of this study was to show that virtual surgical planning (VSP) and printed anatomical models support the reconstruction of the center of rotation (COR) and pelvic BRIM during revision hip surgery using a dual-mobility revision cup system in patients with anterior pelvic column damage and soft tissue envelope deficiency. Methods: Patients with anterior pelvic column damage and soft tissue envelope deficiency underwent revision hip arthroplasty. Virtual planning included assessment of bone segmentation, positioning of the cementless revision cup while maintaining the COR, and the assumed inclination and anteversion angles. Results: The diameter of the planned revision cups was 65.5 ± 2.1 mm, and the diameter of the revision cups used was 65.3 ± 2.1 mm. The difference in COR position in the horizontal axis was 7.8 ± 9.3 mm, in the vertical axis was 4.3 ± 5.9 mm, and in the axial plane was 1.6 ± 3.3 mm. The differences in inclination angle and in the anteversion angle were 12.4° and 8.7°, respectively. Conclusions: The use of VSP and 3D models supports the process of performing RHA surgery in patients with damage to the anterior pelvic column and soft tissue envelope deficiency. Full article
(This article belongs to the Special Issue Computed Tomography Imaging in Medical Diagnosis)
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<p>Representative imaging results (X-ray and CT scan) (Patient No. 6) with marked pelvic BRIM defect (blue line) (<b>A</b>,<b>C</b>); (<b>A</b>) X-ray image before revision surgery; (<b>B</b>) coronal plane image of CT scan before revision surgery; (<b>C</b>) axial plane image of CT scan before revision surgery; (<b>D</b>) segmented pelvic bone with visible structural discontinuity of the iliopectineal line (pelvic BRIM).</p>
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<p>The workflow used in this study and clinical practice. The workflow consists of two main stages of the procedure, i.e., pre-operation evaluation and post-operation evaluation, which include the same steps that need to be performed. During the VSP, a decision is made on the surgical technique to be used and the possible use of a bone allograft. A necessary step in this procedure is to perform X-rays and CT scans before and after the revision surgery.</p>
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<p>Assessment of bone structure segmentation and comparison of the volume of segmented bone structures within the operated pelvis (Patient No. 7): (<b>A</b>) Image of segmented pelvic bones (yellow—damaged side of the pelvis, green—undamaged side of the pelvis) obtained on the basis of CT image analysis. View in the following planes: axial, coronal, and sagittal; (<b>B</b>) comparison of the volume of undamaged (yellow) and damaged (green) pelvic bones before revision surgery; (<b>C</b>) comparison of the volume of undamaged (yellow) and damaged (blue) pelvic bones after revision surgery; (<b>D</b>) comparison of the volume of undamaged sides of the pelvic bone: blue—undamaged pelvic bone after revision surgery, green—undamaged pelvic bone before revision surgery; (<b>E</b>) comparison of the volume of damaged sides of the pelvic bone: blue color—damaged pelvic bone after revision surgery, green color—damaged pelvic bone before revision surgery. The numerical data are shown in <a href="#diagnostics-14-02574-t002" class="html-table">Table 2</a>.</p>
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<p>Virtual COR and pelvic BRIM reconstruction, based on the assumed inclination angle and anteversion angle according to the Lewinnek safe zone, and taking into account the smallest possible bone loss. (<b>A</b>) X-ray image (Patient No. 2)—blue color—marked discontinuity of pelvic BRIM; (<b>B</b>) preoperative CT scan (Patient No. 2). View in the following planes: axial, coronal, and sagittal; segmented bony structures of the pelvis; yellow color—damaged pelvis with bony defect of the anterior column and pubic bone and visible damage to pelvic BRIM; gray color—primary acetabulum and stem with head; (<b>C</b>) virtual surgical planning—virtual reconstruction of the COR and pelvic BRIM based on the assumed inclination angle and anteversion angle according to the Lewinnek safe zone; yellow color—simplified representation of a 68 mm diameter revision cup; (<b>D</b>) photo of a printed model of a damaged pelvis showing the way of measuring the distance between the most important support points for the revision cup. This is characteristic for preoperative planning measurement between the pubic bone and the ischium, and between the acetabular notch and the roof. For the oversizing technique, the quotient is close to 1 (i.e., the ratio of horizontal axis defect distance to vertical axis defect distance in the sagittal plane). Verification of the cup diameter selection using the printed cup gauge—diameter 68 mm (Patient No. 6).</p>
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<p>Postoperative evaluation of the position of the dual-mobility revision cup (Patient No. 6). Blue lines indicate the reconstructed pelvic BRIM. The purple arrow indicates the bone allograft used during the procedure. (<b>A</b>) X-ray image; (<b>B</b>,<b>C</b>) postoperative CT scans; (<b>D</b>) segmented bone structures of the operated cup, with the allograft position marked with an arrow (purple), blue color—dual-mobility revision cup with screws; (<b>E</b>) postoperative analysis of the COR position and inclination and anteversion angles.</p>
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