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A case of mesenteric vein thrombosis developed in the first trimester of pregnancy after in vitro fertilization and embryo transfer in a patient with antiphospholipid syndrome

https://doi.org/10.17749/2313-7347.2018.12.4.072-078

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Abstract

Combined thrombophilia is known as a probable cause of recurrent in vitro fertilization (IVF) failures. The present clinical case demonstrates the importance of considering the possibility of inherited or acquired thrombophilia in patients under the preparation for IVF. Thromboses of rare locations (hepatic vein, splenic vein, mesenteric vein, ovarian vein, retinal vein, cerebral vein, portal vein, axillary and subclavian vein) are life-threatening conditions. Most often thrombosis of atypical location develops in patients with inherited hemostatic defects, e.g. genetic thrombophilia. Such thromboses can also result from acquired abnormalities of hemostasis, which include antiphospholipid syndrome, pregnancy-associated hypercoagulability, IVF, oral contraception, or ovarian hyper-stimulation within IVF procedures.

About the Authors

N. S. Stuleva
I.M. Sechenov First Moscow State Medical University
Russian Federation

PhD, Associate Professor, Department of Obstetrics and Gynecology № 2,

62 St. Zemlyanoi Val, Moscow 109004, Russia

+7(495)7885840



A. V. Vorobiev
I.M. Sechenov First Moscow State Medical University
Russian Federation

PhD, Associate Professor, Department of Obstetrics and Gynecology № 2

62 St. Zemlyanoi Val, Moscow 109004, Russia



E. A. Orudzhova
City Clinical Hospital № 67 named after L.A. Vorokhobov
Russian Federation

PhD, Obstetrician-gynecologist, Head of Center for Ambulatory Medical Care

Russia, 123423 Moscow, Salam Adilya St., 2/44



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For citation:


Stuleva N.S., Vorobiev A.V., Orudzhova E.A. A case of mesenteric vein thrombosis developed in the first trimester of pregnancy after in vitro fertilization and embryo transfer in a patient with antiphospholipid syndrome. Obstetrics, Gynecology and Reproduction. 2018;12(4):72-78. (In Russ.) https://doi.org/10.17749/2313-7347.2018.12.4.072-078

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ISSN 2313-7347 (Print)
ISSN 2500-3194 (Online)