Ibrahim Mohamed N, Liem James, ElKady Ahmed
Department of Diagnostic Radiology, Rotherham General Hospital, Moorgate Road, Rotherham, South Yorkshire S60 2UG, United Kingdom.
Radiol Case Rep. 2020 Oct 3;15(12):2503-2509. doi: 10.1016/j.radcr.2020.09.037. eCollection 2020 Dec.
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.