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Congenital hepatic fibrosis leading to cirrhosis and hepatocellular carcinoma: a case report

机译:先天性肝纤维化导致肝硬化和肝细胞癌:一例报告

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Introduction Congenital hepatic fibrosis is an uncommon cause of portal hypertension. Despite the presence of portal hypertension, hepatocellular and renal function are usually well preserved. Congenital hepatic fibrosis is included in the group of congenital diseases of fibropolycystic disorders. These include a broad spectrum of clinical diseases which are usually accompanied by hepatic involvement. Case presentation We report the case of a 27-year-old Iranian woman with congenital hepatic fibrosis leading to cirrhosis and subsequently hepatocellular carcinoma. Conclusion Advanced cirrhosis was diagnosed and our patient was scheduled for liver transplantation. During preparation for transplant, a hepatic mass was discovered which was found to be hepatocellular carcinoma. Radiofrequency ablation was performed and our patient was referred for transplantation.
机译:简介先天性肝纤维化是门脉高压的罕见原因。尽管存在门脉高压症,但肝细胞和肾功能通常可以很好地保存。先天性肝纤维化包括在纤维多囊性疾病的先天性疾病中。这些包括广泛的临床疾病,通常伴随肝脏受累。病例介绍我们报告了一名27岁的伊朗妇女,该妇女患有先天性肝纤维化,导致肝硬化和随后的肝细胞癌。结论诊断为晚期肝硬化,本例患者计划进行肝移植。在准备移植期间,发现了一块肝脏肿块,被发现是肝细胞癌。进行了射频消融术,我们的患者被转介移植。

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