Takayasu arteritis is a rare primary vasculitis of unknown cause, primarily affecting women of child-bearing age. Its course is unpredictable, but slow progression is usual, leading to stenosis, occlusion, or aneurysmal degeneration of the aorta or its major branches. Poor prognostic factors include retinopathy, secondary hypertension, aortic regurgitation, and arterial aneurysms. Pharmacological treatment is aimed at controlling vessel inflammation and hypertension. We describe the course and management of pregnancy in a woman with severe, complicated Takayasu’s arteritis and review this disease with special reference to natural history, etiopathogenesis, diagnostic criteria, classification, prognostic factors, and treatment strategies.

Target Audience: Obstetricians & Gynecologists, Family Physicians

Leaning Objectives: After completion of this article, the reader should be able to recall the symptoms and hallmarks of Takayasu arteritis, identify potential treatment strategies for Takayasu arteritis in pregnancy, and summarize predictors of poor pregnancy outcomes in women with Takayasu arteritis.