Takayasu's Arteritis: A Case Report

被引:0
|
作者
Khadka, Arzoo [1 ]
Singh, Sumi [2 ]
Timilsina, Sarika [1 ]
机构
[1] Nepal Med Coll & Teaching Hosp, Dept Internal Med, Kathmandu, Nepal
[2] Nepal Police Hosp, Kathmandu, Nepal
关键词
aortitis syndrome; arteritis; case reports; pulseless disease; young female arteritis;
D O I
10.31729/jnma.7685
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Takayasu's arteritis is a chronic vasculitis of medium and large vessels. The most involved vessel is the aorta and its major branches. The disease is primarily seen in young women. The described incidence of the disease ranges from 0.3 to 3.3 million per year. The vessels are characterized by mononuclear infiltration and granulomatous inflammation of vascular media, which leads to arterial wall thickening with stenosis, occlusion, and aneurysmal dilation. Here we present a case of Takayasu's arteritis in a 26-year-old woman who presented with syncope and dizziness with thickened walls of the arch of the aorta and its branches in Magnetic Resonance Imaging angiogram finding. Women of Japanese descent are not the only ones who can develop Takayasu's arteritis; it can affect anyone. Therefore, early diagnosis and treatment are warranted. When the disease is dormant, the outcome seems favourable.
引用
收藏
页码:1041 / 1044
页数:4
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