Journals / Dicle Tıp Dergisi / 2013 / Cilt: 40 - Sayı: 2

The coexistence of focal segmental glomerulosclerosis with carcinoid syndrome: A case report

Karsinoid sendroma eşlik eden fokal segmental glomerüloskleroz: Nadir bir olgu

Pages
326–327
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

We herein present a firs case report of FSGS during follow up of carcinoid syndrome.

📌 3 Key Takeaways

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Objective & Hypothesis:Carcinoid tumor is originated from neuroendocrine tumor family and a rarely presents in humans.
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Key Findings & Data:Membranous and membrano-proliferative glomerulonephritis were rarely reported with presence of carcinoid tumors.
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Conclusion & Impact:We herein present a firs case report of FSGS during follow up of carcinoid syndrome.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

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.

Özet

Karsinoid tümörler nöroendokrin tümör ailesinden olup nadiren karşılaşılmaktadır. Karsinoid sendrom seyrin de 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 sunula caktır.

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Cite This Article

ÜNVERDİ, S., ÇERİ, M., ÜNVERDİ, H., ENSARİ, A., YILMAZ, R., DURANAY, M. (2013). The coexistence of focal segmental glomerulosclerosis with carcinoid syndrome: A case report. Dicle Tıp Dergisi, Cilt: 40 - Sayı: 2, 326–327. https://ajindex.com/articles/349565

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