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一名白人青少年冠状动脉高安动脉炎表现为猝死

Takayasu Arteritis of the Coronary Arteries Presenting as Sudden Death in a White Teenager.

作者信息

Hlavaty Leigh, Diaz Francisco, Sung LokMan

机构信息

From the Department of Pathology, University of Michigan, Ann Arbor; and the Wayne County Medical Examiner's Office, Detroit, MI.

出版信息

Am J Forensic Med Pathol. 2015 Sep;36(3):221-3. doi: 10.1097/PAF.0000000000000179.

Abstract

Takayasu arteritis is a rare disease that expresses chronic, large vessel inflammation. The etiology remains unclear and its presentation depends on the affected arteries. With coronary artery involvement, manifestations range from chest pain and shortness of breath to sudden death. We report a case of a 15-year-old white girl who presented with syncope immediately before passing. On autopsy, all 3 major coronary arteries grossly contained multiple proximal lesions that were consistent with Takayasu arteritis, microscopically. Takayasu arteritis solely affecting multiple coronary arteries is exceedingly rare. This report discusses the significance of coronary involvement in Takayasu arteritis at autopsy and sudden death.

摘要

高安动脉炎是一种罕见的疾病,表现为慢性大血管炎症。病因尚不清楚,其表现取决于受累动脉。当冠状动脉受累时,表现范围从胸痛、呼吸急促到猝死。我们报告一例15岁白人女孩病例,她在临终前出现晕厥。尸检时,所有3支主要冠状动脉大体上均有多个近端病变,显微镜检查符合高安动脉炎。高安动脉炎单独累及多支冠状动脉极为罕见。本报告讨论了高安动脉炎尸检时冠状动脉受累及猝死的意义。

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