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遗传性出血性毛细血管扩张症。一例合并肝细胞癌及获得性肝脑变性的病例。

Hereditary hemorrhagic telangiectasia. A case with hepatocellular carcinoma and acquired hepatocerebral degeneration.

作者信息

Sussman E B, Sternberg S S

出版信息

Arch Pathol. 1975 Feb;99(2):95-100.

PMID:163631
Abstract

A patient with hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease), treated with ethinyl estradiol, multiple blood transfusions, and iron-dextran, developed hepatocellular carcinoma and acquired hepatocerebral degeneration. In addition to the carcinoma, the liver contained extensive arteriovenous maliformations, telangiectasis, and changes of Osler atypical cirrhosis. The carcinoma possibly had its genesis in the presence of an ocongenic serum hepatitis virus, or the cirrhosis, or both.

摘要

一名患有遗传性出血性毛细血管扩张症(奥斯勒-韦伯-伦杜病)的患者,接受了炔雌醇、多次输血和右旋糖酐铁治疗,之后发生了肝细胞癌并出现了获得性肝脑变性。除了癌症外,肝脏还存在广泛的动静脉畸形、毛细血管扩张以及奥斯勒非典型肝硬化的改变。该癌症可能起源于先天性血清肝炎病毒的存在、肝硬化,或两者皆有。

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