Stenting in Takayasu’s arteritis: A Case report

Takayasu arteritis (TA), also known as idiopathic medial aortopathy or pulseless disease, is a
granulomatous large vessel vasculitis that predominantly affects the aorta and its major branches. It may
also affect the pulmonary arteries. The exact cause is not well known but the pathology is thought to be
similar to giant cell arteritis. There is segmental and patch granulomatous inflammation of the aorta which
results in stenosis, thrombosis and aneurysm formation. Half of the patients present with an initial systemic
illness whereas the other 50% present with late-phase complications. There is a strong female
predominance (F: M ~ 9:1), an increased prevalence in Asian populations, and it tends to affect younger
patients (<50 years of age). The typical age of onset is at around 15-30 years of age. Here, it is reported a
case of 9 years old girl with Takayasu’s arteritis.

 

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