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Journals / Harran Üniversitesi Tıp Fakültesi Dergisi / 2020 / Cilt: 17 - Sayı: 3

Newly Diagnosed Patient with Primary Biliary Cholangitis: Case Report

Yeni Tanı Primer Biliyer Kolanjitli Hasta: Olgu Sunumu

Nuray KIVANÇ TERZİ
Mehmet Sidar GÜLER
Dursun ÇADIRCI
Ahmet UYANIKOĞLU
Pages
492–494
Publication Date
2020-12-25
DOI
—
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AI Summary & Key Takeaways

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

As in this case, it should not be forgotten that it may come with non-specific symptoms, detailed history and diagnosis should be confirmed with necessary laboratory tests in patients suspected.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Primary biliary cholangitis (PBC) is a slowly progressive chronic cholestatic granulomatous liver disease of unknown etiology, mostly affected by middle-aged women, accompanied by damage to the small bile ducts.
📊
Key Findings & Data:PBK can cause serious diseases such as portal hypertension or liver failure and then progress to cirrhosis.
💡
Conclusion & Impact:As in this case, it should not be forgotten that it may come with non-specific symptoms, detailed history and diagnosis should be confirmed with necessary laboratory tests in patients suspected.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:PBK · AMA · kaşıntı

Abstract

Primary biliary cholangitis (PBC) is a slowly progressive chronic cholestatic granulomatous liver disease of unknown etiology, mostly affected by middle-aged women, accompanied by damage to the small bile ducts. PBK can cause serious diseases such as portal hypertension or liver failure and then progress to cirrhosis. As in this case, it should not be forgotten that it may come with non-specific symptoms, detailed history and diagnosis should be confirmed with necessary laboratory tests in patients suspected.

Özet

Primer biliyer kolanjit (PBK) etiyolojisi bilinmeyen, çoğunlukla orta yaş kadınların etkilendiği, küçük safra kanallarında hasarın eşlik ettiği, yavaş ilerleyen, kronik kolestatik granülomatöz bir karaciğer hastalığıdır. PBK, portal hipertansiyon veya karaciğer yetmezliği gibi ciddi hastalıklara neden olup sonrasında siroza ilerleyebilir. Bu vakada olduğu gibi non-spesifik semptomlarla gelebileceği unutulmamalı, ayrıntılı anamnez ve şüphelenilen hastalarda gerekli laboratuvar tetkikleri ile tanı kesinleştirilmelidir.

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Cite This Article

TERZİ, N. K., GÜLER, M. S., ÇADIRCI, D., UYANIKOĞLU, A. (2020). Newly Diagnosed Patient with Primary Biliary Cholangitis: Case Report. Harran Üniversitesi Tıp Fakültesi Dergisi, Cilt: 17 - Sayı: 3, 492–494. https://ajindex.com/articles/88111

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