Case of Thrombosis of Rare Localization in a Cancer Patient with Combined form of Thrombophilia
Vorobev A, Makatsaria A*, Bitsadze V, Khamani N and Udovychenko M
Department of Obstetrics and Gynecology, First Moscow State Medical Sechenov, University of the Ministry of Health Russian Federation, Russia
- *Corresponding Author:
- Makatsaria A
Department of Obstetrics and Gynecology
First Moscow State Medical Sechenov
University of the Ministry of Health
Russian Federation, Russia
Received Date: May 17, 2017 Accepted Date: June 15, 2017 Published Date: June 19, 2017
Citation: Vorobev A, Makatsaria A, Bitsadze V, Khamani N, Udovychenko M (2017) Case of Thrombosis of Rare Localization in a Cancer Patient with Combined form of Thrombophilia. J Cancer Sci Ther 9: 492-495. doi: 10.4172/1948-5956.1000465
Copyright: © 2017 Vorobev A, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Thrombosis can be a clinical symptom of hidden cancer, as evidenced by numerous studies. Inherited and acquired thrombophilia are well-known risk factors for venous thromboembolism. The incidence of thrombotic events in cancer patients is increased compared to normal population. Data on inherited thrombophilia and cancer is limited. In most cases, a key role in the pathogenesis of thrombosis of rare localization is played by hereditary thrombophilia. Clinically, venous thromboembolism and cancer are almost always closely interrelated, and often thrombosis can be the only clinical symptom of latent cancer. Here in this case report, we present a case of thrombosis of rare localization in a cancer patient with combined form of thrombophilia.