Takayasu’s arteritis is a chronic inflammatory, autoimmune, granulomatous disease of the aorta and its major branches, at their origin, resulting in dilatation, occlusion, stenosis and/or aneurysm formation of these arteries. The disease usually begins in adulthood but pediatric involvement is very rare and the diagnosis is late. We report the case of a 13-year-old child admitted for respiratory distress, whose detailed clinical examination and CT angiography confirmed the diagnosis.
Cite this paper
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