@article{Dağdeviren_Cengiz_Çaypınar_Kaya_Kanawati_2014, place={Ankara, TR}, title={Atypical HELLP Syndrome in a Pregnant Patient with Takayasu Arteritis and Subclavian to Axillary Artery Saphenous Vein Bypass Graft: A Case Report}, volume={20}, url={https://www.gorm.com.tr/index.php/GORM/article/view/165}, abstractNote={<p>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.</p>}, number={3}, journal={Gynecology Obstetrics & Reproductive Medicine}, author={Dağdeviren, Hediye and Cengiz, Hüseyin and Çaypınar, Sema Süzen and Kaya, Cihan and Kanawati, Ammar}, year={2014}, month={Dec.}, pages={163–165} }