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Multiple endocrine neoplasia type 1 (MEN1) presenting with renal stones: Case report and review

Radiol Case Rep. 2020 Oct 3;15(12):2503-2509. doi: 10.1016/j.radcr.2020.09.037. eCollection 2020 Dec.

Abstract

Multiple endocrine neoplasia type 1 (MEN1) is a complex, autosomal dominant inherited syndrome characterized by 3 different tumors (parathyroid, anterior pituitary, and pancreatic islet). The diagnosis is defined clinically by the presence of 2 or more primary tumors. We report the case of a 35 years old patient who presented with recurrent renal stones and imaging findings for MEN1. Computed tomography pancreas revealed a mass in the tail which was confirmed by magnetic resonance imaging. Ultrasound of her neck showed a mass on the left side and MIBI scan diagnosed a parathyroid adenoma which was later pathologically confirmed.

Keywords: Multiple endocrine neoplasia type 1; Pancreatic neuroendocrine tumors; Parathyroid adenoma; Prolactinoima; Renal stones.

Publication types

  • Case Reports