1例报告:b型畸形。

IF 1.1 4区 医学 Q4 GASTROENTEROLOGY & HEPATOLOGY
Chen Zeng , Hanjiang Zeng , Yehan Li , Bing Wu
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引用次数: 0

摘要

先天性肝外门系统分流,又称阿伯内蒂畸形,是一种罕见的解剖性血管畸形。Abernethy畸形患者可能表现为腹痛、肝功能异常、肝肺综合征、肺动脉高压和/或门系统性脑病。准确识别分流和门静脉并有效处理并发症对这些患者至关重要。常规影像学检查对Abernethy畸形的诊断和分类是有用的。然而,这些检查可能会遗漏一些门静脉分支。在这种情况下,当常规成像不能准确识别肝门静脉时,数字减影血管造影是非常宝贵的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Case Report: Type Ib Abernethy malformation
Congenital extrahepatic portosystemic shunt, also known as Abernethy malformation, is a rare anatomic vascular malformation. Patients with Abernethy malformation may present with abdominal pain, abnormal liver function tests, hepatopulmonary syndrome, pulmonary hypertension, and/or portosystemic encephalopathy. Accurate identification of the shunt and portal vein and effective management of complications is vital in these patients. Routine imaging examinations are useful for the diagnosis and classification of Abernethy malformation. However, these examinations may miss some portal vein branches. Digital subtraction angiography is invaluable when routine imaging cannot precisely identify the hepatic portal vein in this situation.
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来源期刊
Arab Journal of Gastroenterology
Arab Journal of Gastroenterology Medicine-Gastroenterology
CiteScore
2.70
自引率
0.00%
发文量
52
期刊介绍: Arab Journal of Gastroenterology (AJG) publishes different studies related to the digestive system. It aims to be the foremost scientific peer reviewed journal encompassing diverse studies related to the digestive system and its disorders, and serving the Pan-Arab and wider community working on gastrointestinal disorders.
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