Journals / Şişli Etfal Hastanesi Tıp Bülteni / 2005 / Cilt: 39 - Sayı: 3

Fibrolamellar type hepatocellular carcinoma

Fibrolamellar tip hepatosellüler karsinoma

Pages
49–52
DOI
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AI Summary & Key Takeaways

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

The patient was regarded as unresectable due to extrahepatic disease and underwent to chemotherapy.

📌 3 Key Takeaways

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Objective & Hypothesis:Fibrolamellar type hepatocellular carcinoma is a rare malignant, tumor that has distinctive clinical, radiological, histological and prognostic features in comparison to conventional hepatocellular carcinoma.
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Key Findings & Data:In our case report, we describe a 28 year old male who has no history of chirrhosis.
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Conclusion & Impact:The patient was regarded as unresectable due to extrahepatic disease and underwent to chemotherapy.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Biyopsi · Manyetik rezonans görüntüleme · Erkek

Abstract

Fibrolamellar type hepatocellular carcinoma is a rare malignant, tumor that has distinctive clinical, radiological, histological and prognostic features in comparison to conventional hepatocellular carcinoma. In our case report, we describe a 28 year old male who has no history of chirrhosis. In a routine laboratory examination, liver enzymes were found abnormal and ultrasono graphic examination revealed, a huge liver mass. Magnetic resonance imaging demonstrated typical features of these tumors which include large lobulated mass, early hetewgenous dense enhancement, santral scar tissue and extrahepatic malignant lymph nodes. Following core biopsy, histopathologic examination confirmed the diagnosis. The patient was regarded as unresectable due to extrahepatic disease and underwent to chemotherapy.

Özet

Fibrolamellar tip hepatosellüler karsinoma nadir görülen hir tümör olup, konvansiyonel hepatosellüler karsinomaya kıyasla ayırt ettirici klinik, radyolojik, histolojik ve prognostik özelliklere sahiptir. Biz olgu bildirimizde özgeçmişinde siroz hikayesi olmayan 28 yaşındaki bir erkek hastayı tanımladık. Hastanın rutin laboratuvar Muayenesinde karaciğer enzimleri, yüksekti ve yapılan ultrasonografide büyük karaciğer kitlesi tespit edildi. Manyetik rezonans görüntüleme ile bu tümörler için tipik olan büyük lobüle şekilli kitle lezyonu, erken fazda yoğun heterojen kontrast tutulumu, santral skar dokusu ve ekstrahepatik malign'lenf nodlün ortaya kondu. Core biyopsisini takiben yapılan'histopatolojik inceleme ile fibrolamellar tip hepatosellüler karsinoma tanısı doğrulandı. Hasta karaciğer dışı hastalık yayılımı nedeniyle rezeksiyona uygun bulunmadı ve kemoterapiye gönderildi.

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Cite This Article

HALEFOĞLU, A. M., YILDIZ, E., KARPAT, Z. (2005). Fibrolamellar type hepatocellular carcinoma. Şişli Etfal Hastanesi Tıp Bülteni, Cilt: 39 - Sayı: 3, 49–52. https://ajindex.com/articles/363530

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