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Acquired Hemophilia A Presenting as Intramuscular Hematoma

Acquired hemophilia A poses a clinical and diagnostic challenge. Although rare, it is still the most common acquired factor deficiency. We present a case of acquired hemophilia A diagnosed in a 71-year-old female who presented with a right thigh hematoma of acute onset. The diagnosis was established...

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Detalles Bibliográficos
Autores principales: Al-Shbool, Ghassan, Vakiti, Anusha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299309/
https://www.ncbi.nlm.nih.gov/pubmed/30574513
http://dx.doi.org/10.1177/2324709618817572
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author Al-Shbool, Ghassan
Vakiti, Anusha
author_facet Al-Shbool, Ghassan
Vakiti, Anusha
author_sort Al-Shbool, Ghassan
collection PubMed
description Acquired hemophilia A poses a clinical and diagnostic challenge. Although rare, it is still the most common acquired factor deficiency. We present a case of acquired hemophilia A diagnosed in a 71-year-old female who presented with a right thigh hematoma of acute onset. The diagnosis was established based on the coagulation profile along with factor VIII levels, mixing studies, and inhibitor levels. The patient received multiple lines of therapy including steroids, factor VIIa, Obizur (porcine-derived recombinant factor VIII), followed by multiple cycles of chemotherapy including cyclophosphamide and rituximab.
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spelling pubmed-62993092018-12-20 Acquired Hemophilia A Presenting as Intramuscular Hematoma Al-Shbool, Ghassan Vakiti, Anusha J Investig Med High Impact Case Rep Case Report Acquired hemophilia A poses a clinical and diagnostic challenge. Although rare, it is still the most common acquired factor deficiency. We present a case of acquired hemophilia A diagnosed in a 71-year-old female who presented with a right thigh hematoma of acute onset. The diagnosis was established based on the coagulation profile along with factor VIII levels, mixing studies, and inhibitor levels. The patient received multiple lines of therapy including steroids, factor VIIa, Obizur (porcine-derived recombinant factor VIII), followed by multiple cycles of chemotherapy including cyclophosphamide and rituximab. SAGE Publications 2018-12-06 /pmc/articles/PMC6299309/ /pubmed/30574513 http://dx.doi.org/10.1177/2324709618817572 Text en © 2018 American Federation for Medical Research http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (http://www.creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Al-Shbool, Ghassan
Vakiti, Anusha
Acquired Hemophilia A Presenting as Intramuscular Hematoma
title Acquired Hemophilia A Presenting as Intramuscular Hematoma
title_full Acquired Hemophilia A Presenting as Intramuscular Hematoma
title_fullStr Acquired Hemophilia A Presenting as Intramuscular Hematoma
title_full_unstemmed Acquired Hemophilia A Presenting as Intramuscular Hematoma
title_short Acquired Hemophilia A Presenting as Intramuscular Hematoma
title_sort acquired hemophilia a presenting as intramuscular hematoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299309/
https://www.ncbi.nlm.nih.gov/pubmed/30574513
http://dx.doi.org/10.1177/2324709618817572
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