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以肺动脉高压为表现的高安动脉炎。

Takayasu's arteritis presenting as pulmonary hypertension.

作者信息

Haas A, Stiehm E R

出版信息

Am J Dis Child. 1986 Apr;140(4):372-4. doi: 10.1001/archpedi.1986.02140180106036.

Abstract

Takayasu's arteritis (pulseless disease) is a vasculitis that affects the large arteries, including the aorta, its branches, and the pulmonary arteries. A 15-year-old girl with Takayasu's arteritis was referred to our institution for marked pulmonary hypertension in the absence of symptoms referable to systemic vasculitis. She was shown to have a thickened, narrowed thoracic aorta, a stenosed right axillary artery, and severely affected pulmonary arteries. Despite corticosteroid therapy she died one month after diagnosis. This patient's illness indicates that pulmonary vessels might be the principal vessels involved in Takayasu's arteritis.

摘要

高安动脉炎(无脉症)是一种累及大动脉的血管炎,这些大动脉包括主动脉、其分支以及肺动脉。一名患有高安动脉炎的15岁女孩因出现明显的肺动脉高压但无系统性血管炎相关症状而被转诊至我院。检查发现她的胸主动脉增厚、变窄,右腋动脉狭窄,肺动脉严重受累。尽管接受了皮质类固醇治疗,但她在诊断后一个月死亡。该患者的病情表明,肺血管可能是高安动脉炎主要累及的血管。

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