Afshar Reza, Sanavi Suzan, Taheri Hamid-Reza
Department of Nephrology, University of Social Welfare & Rehabilitation Sciences, Tehran, Iran.
Saudi J Kidney Dis Transpl. 2012 Jan;23(1):117-21.
Multiple endocrine neoplasia (MEN) is a group of heritable syndromes characterized by aberrant growth of benign or malignant tumors in a subset of endocrine tissues. There are three major syndromes: MEN1, 2A and 2B. We describe a 60-year-old woman who initially manifested acute renal failure due to hypercalcemia and dehydration and, finally, was diagnosed as a sporadic MEN1 case.
多发性内分泌腺瘤病（MEN）是一组遗传性综合征，其特征是内分泌组织的一个子集中出现良性或恶性肿瘤的异常生长。有三种主要综合征：MEN1、2A和2B。我们描述了一名60岁女性，她最初因高钙血症和脱水表现为急性肾衰竭，最终被诊断为散发性MEN1病例。
