Carcinoid tumor is originated from neuroendocrine tumor family and a rarely presents in humans. Membranous and membrano-proliferative glomerulonephritis were rarely reported with presence of carcinoid tumors. However, the coexistence of focal segmental glomerulosclerosis (FSGS) with carcinoid syndrome have not been defined previously. We herein present a firs case report of FSGS during follow up of carcinoid syndrome.
Karsinoid tümörler nöroendokrin tümör ailesinden olup nadiren karşılaşılmaktadır. Karsinoid sendrom seyrinde membranöz glomerülonefrit ve membrano-proliferatif glomerülonefrit olguları tanımlanmakla birlikte, karsinoid sendrom ile fokal segmental glomerüloskleroz (FSGS) birlikteliği daha önce tanımlanmamıştır. Burada ilk kez tanımlanan karsinoid sendrom FSGS birlikteliği sunulacaktır.
Primary Language | Turkish |
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Journal Section | Case Reports |
Authors | |
Publication Date | June 1, 2013 |
Submission Date | March 2, 2015 |
Published in Issue | Year 2013 Volume: 40 Issue: 2 |