| Literature DB >> 26110486 |
Leigh Hlavaty1, Francisco Diaz, LokMan Sung.
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.Entities:
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Year: 2015 PMID: 26110486 DOI: 10.1097/PAF.0000000000000179
Source DB: PubMed Journal: Am J Forensic Med Pathol ISSN: 0195-7910 Impact factor: 0.921