Literature DB >> 26110486

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

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:  

Mesh:

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


  3 in total

1.  Portal hypertension: an uncommon clinical manifestation of Takayasu arteritis in a 9-year-old child.

Authors:  Cristina N Herrera; Javier E Tomala-Haz
Journal:  Open Access Rheumatol       Date:  2016-11-15

2.  Cause of death in Chinese Takayasu arteritis patients.

Authors:  Jing Li; Mengzhu Zhu; Mengtao Li; Wenjie Zheng; Jiuliang Zhao; Xinping Tian; Xiaofeng Zeng
Journal:  Medicine (Baltimore)       Date:  2016-07       Impact factor: 1.889

3.  Serum concentrations of small dense low-density lipoprotein cholesterol and lipoprotein(a) are related to coronary arteriostenosis in Takayasu arteritis.

Authors:  Si Chen; Haixia Luan; Jianxun He; Yan Wang; Shuang Liu; Yongzhe Li; Xiaoli Zeng; Hui Yuan
Journal:  J Clin Lab Anal       Date:  2021-10-28       Impact factor: 2.352

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.