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Spontaneous deep vein thrombosis in hemophilia A: a case report

Venous thromboembolus is an important cause of hospital acquired morbidity and mortality. Venous thrombosis is a very rare occurrence in patients with haemophilia A. The thrombosis originated from the right main and external iliac veins, and effects the cranial segments of the main, deep and superfi...

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Detalles Bibliográficos
Autores principales: Bicer, Murat, Yanar, Murat, Tuydes, Oktay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3444229/
https://www.ncbi.nlm.nih.gov/pubmed/20181150
http://dx.doi.org/10.4076/1757-1626-2-6390
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author Bicer, Murat
Yanar, Murat
Tuydes, Oktay
author_facet Bicer, Murat
Yanar, Murat
Tuydes, Oktay
author_sort Bicer, Murat
collection PubMed
description Venous thromboembolus is an important cause of hospital acquired morbidity and mortality. Venous thrombosis is a very rare occurrence in patients with haemophilia A. The thrombosis originated from the right main and external iliac veins, and effects the cranial segments of the main, deep and superficial femoral veins as an acute phase thrombus. Neither any local anatomic compression nor any predisposing thrombophilic risk factors were identified. We treated the patient with enoxaparine 1 mg/kg twice a day subcutaneously and then started oral anticoagulation with warfarin.
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spelling pubmed-34442292012-09-18 Spontaneous deep vein thrombosis in hemophilia A: a case report Bicer, Murat Yanar, Murat Tuydes, Oktay Cases J Case Report Venous thromboembolus is an important cause of hospital acquired morbidity and mortality. Venous thrombosis is a very rare occurrence in patients with haemophilia A. The thrombosis originated from the right main and external iliac veins, and effects the cranial segments of the main, deep and superficial femoral veins as an acute phase thrombus. Neither any local anatomic compression nor any predisposing thrombophilic risk factors were identified. We treated the patient with enoxaparine 1 mg/kg twice a day subcutaneously and then started oral anticoagulation with warfarin. BioMed Central 2009-09-11 /pmc/articles/PMC3444229/ /pubmed/20181150 http://dx.doi.org/10.4076/1757-1626-2-6390 Text en Copyright ©2009 Bicer et al.; licensee Cases Network Ltd. licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Bicer, Murat
Yanar, Murat
Tuydes, Oktay
Spontaneous deep vein thrombosis in hemophilia A: a case report
title Spontaneous deep vein thrombosis in hemophilia A: a case report
title_full Spontaneous deep vein thrombosis in hemophilia A: a case report
title_fullStr Spontaneous deep vein thrombosis in hemophilia A: a case report
title_full_unstemmed Spontaneous deep vein thrombosis in hemophilia A: a case report
title_short Spontaneous deep vein thrombosis in hemophilia A: a case report
title_sort spontaneous deep vein thrombosis in hemophilia a: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3444229/
https://www.ncbi.nlm.nih.gov/pubmed/20181150
http://dx.doi.org/10.4076/1757-1626-2-6390
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