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.
多发性内分泌腺瘤1型(MEN1)是一种复杂的常染色体显性遗传综合征,其特征为3种不同肿瘤(甲状旁腺、垂体前叶和胰岛)。临床诊断依据为存在2个或更多原发性肿瘤。我们报告1例35岁患者,该患者因复发性肾结石及MEN1的影像学表现前来就诊。胰腺计算机断层扫描显示胰尾有一肿块,磁共振成像证实了这一情况。其颈部超声显示左侧有一肿块,甲氧基异丁基异腈扫描诊断为甲状旁腺腺瘤,随后经病理证实。