alexa Spontaneous Subcutaneous and Muscular Bleeding due to Acquired Hemophilia A in Association with Poorly-Controlled Asthma: A Case Report
ISSN: 2165-7831

Journal of Blood & Lymph
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Case Report

Spontaneous Subcutaneous and Muscular Bleeding due to Acquired Hemophilia A in Association with Poorly-Controlled Asthma: A Case Report

Askin D1*, Baskin M2 and Levine RL3

1Lenox Hill Hospital, Department of Hematology and Oncology, NY, USA

2St Lukes-Roosevelt Hospital, Department of Pulmonary Medicine, NY, USA

3Lenox Hill Hospital, Director of Blood Bank, NY, USA

*Corresponding Author:
Askin D
Department of Hematology and Oncology
Lenox Hill Hospital, NY, USA
E-mail: [email protected]

Received Date: May 10, 2012; Accepted Date: May 29, 2012; Published Date: May 31, 2012

Citation: Askin D, Baskin M, Levine RL (2012) Spontaneous subcutaneous and muscular bleeding due to Acquired Hemophilia a in Association with Poorly- Controlled Asthma: A Case Report. J Blood Lymph 2:107.doi:10.4172/2165-7831.1000107

Copyright: © 2012 Askin D, 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.

 

Abstract

Acquired hemophilia A is due to the development of autoantibodies to factor VIII, which can occur spontaneously in healthy individuals or secondary to autoimmune disorders, drugs, malignancy, or the post-partum period. It has also been described in the literature to develop in association with asthma. Given the high incidence of asthma, healthcare providers should be aware of the association between this common condition and the much less common acquired factor VIII deficiency, a serious bleeding disorder with significant morbidity. The presentation of patients acquiring factor VIII deficiency will depend on the level of the inhibitor present, which is inversely proportional to the percentage of active factor VIII available for hemostasis. This paper describes a patient with poorly controlled asthma who acquired a factor VIII inhibitor at the age of 70.

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