Author/Authors :
Afshar, Reza shahed university - Mustafa Khomeini Hospital - Department of Nephrology, تهران, ايران , Sanavi, Suzan university of social welfare and rehabilitation sciences - Clinical Department, ايران , Taheri, Hamid-Reza shahed university - Mustafa Khomeini Hospital - Department of Vascular Surgery, تهران, ايران
Abstract :
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.
