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Pulmonary arteriovenous malformation in Osler-Weber-Rendu syndrome

机译:Osler-Weber-Rendu综合征的肺动静脉畸形

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摘要

Osler-Weber-Rendu syndrome, also known as hereditary hemorrhagic telangiectasia, is an autosomal dominant disorder typically identified by the triad of telangiectasia, recurrent epistaxis, and a positive family history of the disorder. A 45-year-old man presented with/ recurrent epistaxis and gastrointestinal bleeding. Chest computed tomography (Figure 1) and multidetector computed tomography angiography (Figure 2) confirmed a right pulmonary arteriovenous malformation. The patient was successfully treated by a right middle lobectomy.
机译:Osler-Weber-Rendu综合征,也称为遗传性出血性毛细血管扩张,是一种常染色体显性遗传疾病,通常由毛细血管扩张三联征,复发性鼻identified和该疾病的阳性家族史确定。一名45岁的男子出现鼻出血/反复发作和胃肠道出血。胸部计算机断层扫描(图1)和多探测器计算机断层扫描血管造影(图2)证实右肺动静脉畸形。该患者已通过右中叶切除术成功治疗。

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