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Takayasu arteritis (TA) is a rare chronic granulomatous inflammatory disease of the aorta and/or its major branches, affecting mostly the vertebral, carotid, subclavian, iliac, and renal arteries. The disease shows a striking predilection for women during the child-bearing years, and it is reasonable to expect at least 1 pregnancy event in these women. Therefore, the management of pregnancies in patients with this disease is of great importance to obstetricians. Here, we present the case of a patient with atypical hemolysis, elevated liver enzymes, and low platelets (HELLP syndrome); this patient was receiving corticosteroid therapy and had undergone subclavian-axillary artery saphenous vein graft for TA.
Alan : Sağlık Bilimleri
Dergi Türü : Uluslararası
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