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

Am J Forensic Med Pathol

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

Published: September 2015

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.

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Source
http://dx.doi.org/10.1097/PAF.0000000000000179DOI Listing

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