Abernethy syndrome as a cause of liver transplantation.

IF 2.7 4区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Angélica Blanco Rodríguez, Dora Gómez Pasantes, Mónica Torres Díaz, Irene Aguirrezabalaga Martínez, Carla Madarro Pena, Aloia Guerreiro Caamaño, Javier Aguirrezabalaga González, Manuel Gómez Gutiérrez
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引用次数: 0

Abstract

Congenital portosystemic shunts are rare abnormalities in which blood flow from the liver is diverted to the systemic circulation. We would like to present the case of a 48-year-old male, during his neurological follow-up he was diagnosed with a congenital intrahepatic portosystemic shunt. Embolization of the portosystemic communicating veins was attempted on two occasions, but without success. Due to the poor clinical course, the patient was presented to our transplant committee and a liver transplant was decided upon.

作为肝移植病因的阿伯内西综合征。
先天性门静脉分流是一种罕见的异常现象,在这种情况下,来自肝脏的血流会转向全身循环。我们要介绍的是一名 48 岁男性的病例,他在神经系统随访期间被诊断出患有先天性肝内门体分流。曾两次尝试栓塞门静脉分流静脉,但均未成功。由于临床症状不佳,患者被提交给我们的移植委员会,并决定进行肝移植。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.00
自引率
25.00%
发文量
400
审稿时长
6-12 weeks
期刊介绍: La Revista Española de Enfermedades Digestivas, Órgano Oficial de la Sociedad Española de Patología Digestiva (SEPD), Sociedad Española de Endoscopia Digestiva (SEED) y Asociación Española de Ecografía Digestiva (AEED), publica artículos originales, editoriales, revisiones, casos clínicos, cartas al director, imágenes en patología digestiva, y otros artículos especiales sobre todos los aspectos relativos a las enfermedades digestivas.
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