遗传性出血性毛细血管扩张的肝血管变异

Q3 Medicine
Sultan Qaboos University Medical Journal Pub Date : 2023-11-01 Epub Date: 2023-11-30 DOI:10.18295/squmj.1.2023.011
Alamelu Alagappan, Biswajit Sahoo, Jain H Prakash, Manas K Panigrahi, Taraprasad Tripathy
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引用次数: 0

摘要

遗传性出血性毛细血管扩张症(HHT)是一种常染色体显性遗传病,以血管发育不良为特征。肝血管畸形(vm)的范围从小的毛细血管扩张到明显的血管分流。我们在此报告两例HHT病例。病例1为肝动脉沿肝内及肝外扩散扩张伴肝动脉瘤。病例2表现为回肠和肝毛细血管扩张。这些血管变异的知识是必不可少的临床医生和放射科医生在辅助诊断和手术和介入管理。关键词:血管畸形,HHT,动静脉畸形,回肠毛细血管扩张。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hepatic Vascular Variants in Hereditary Haemorrhagic Telangiectasia: Imaging findings.

Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder characterised by vascular dysplasia. Hepatic vascular malformations (VMs) range from small telangiectases to significant vascular shunting. Here we report two cases of HHT. Case 1 had diffuse ectasia of the hepatic artery along its intrahepatic and extrahepatic course with a hepatic arterial aneurysm. Case 2 presented with ileal and hepatic telangiectases. Knowledge of these vascular variants is indispensable for clinicians and radiologists in aiding diagnosis and surgical and interventional management.

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来源期刊
CiteScore
2.00
自引率
0.00%
发文量
86
审稿时长
7 weeks
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