奥斯勒-伦杜-韦伯合并肝脏受累。

Journal belge de radiologie Pub Date : 1998-08-01

H Goris, E Heindryckx, L Van Hoe, L Stockx, G Marchal, M Deceuninck

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引用次数: 0

摘要

奥斯勒-伦度-韦伯病，或遗传性出血性毛细血管扩张症，是一种常染色体显性遗传的血管疾病。31%的遗传性出血性毛细血管扩张患者累及肝脏(1)。这种病变似乎很少引起严重疾病。我们报告一例肝脏广泛毛细血管扩张的影像学表现和治疗。

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Osler-Rendu-Weber with liver involvement.

Osler-Rendu-Weber disease, or hereditary hemorrhagic telangiectasia, is a vascular disease with autosomal dominant transmission. The liver is involved in 31% of patients with hereditary hemorrhagic telangiectasia (1). It appears that the lesions uncommonly causes serious disease. We report the imaging findings and the therapy in a case with extensive telangiectasis in the liver.

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Journal belge de radiologie

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