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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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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. |
format | Online Article Text |
id | pubmed-3444229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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