The prognosis and treatment of acquired hemophilia: a systematic review and meta-analysis

2009 ◽  
Vol 20 (7) ◽  
pp. 517-523 ◽  
Author(s):  
Rhonda L Bitting ◽  
Stephen Bent ◽  
Yongmei Li ◽  
Jeffrey Kohlwes
Keyword(s):  
Systematic Review ◽  
Hemophilia A ◽  
Meta Analysis ◽  
Acquired Hemophilia A ◽  
Acquired Hemophilia

Acquired Hemophilia A in Aged People: A Systematic Review of Case Reports and Case Series

2018 ◽  
Vol 55 (4) ◽  
pp. 197-201 ◽  
Author(s):  
Lidvine Godaert ◽  
Seendy Bartholet ◽  
Sébastien Colas ◽  
Lukshe Kanagaratnam ◽  
Jean-Luc Fanon ◽  
...  
Keyword(s):  
Systematic Review ◽  
Hemophilia A ◽  
Case Reports ◽  
Case Series ◽  
Acquired Hemophilia A ◽  
Acquired Hemophilia ◽  
Aged People

scholarly journals Immunoadsorption for the Treatment of Acquired Hemophilia: New Observational Data, Systematic Review, and Meta-Analysis

2021 ◽  
Author(s):  
Michael Esteves Pereira ◽  
Christoph Bocksrucker ◽  
Johanna Anna Kremer Hovinga ◽  
Martin Mueller ◽  
Michael Daskalakis ◽  
...  
Keyword(s):  
Systematic Review ◽  
Observational Data ◽  
Meta Analysis ◽  
Acquired Hemophilia

scholarly journals Successful Management of Acquired Hemophilia A Associated with Bullous Pemphigoid: A Case Report and Review of the Literature

2017 ◽  
Vol 2017 ◽  
pp. 1-7 ◽  
Author(s):  
Quentin Binet ◽  
Catherine Lambert ◽  
Laurine Sacré ◽  
Stéphane Eeckhoudt ◽  
Cedric Hermans
Keyword(s):  
Bullous Pemphigoid ◽  
Neutralizing Antibodies ◽  
Hemophilia A ◽  
Rare Condition ◽  
Term Treatment ◽  
Acquired Hemophilia A ◽  
Acquired Hemophilia ◽  
Short Term Treatment ◽  
Life Threatening ◽  
Dose Levels

Background. Acquired hemophilia A (AHA) is a rare condition, due to the spontaneous formation of neutralizing antibodies against endogenous factor VIII. About half the cases are associated with pregnancy, postpartum, autoimmune diseases, malignancies, or adverse drug reactions. Symptoms include severe and unexpected bleeding that may prove life-threatening.Case Study. We report a case of AHA associated with bullous pemphigoid (BP), a chronic, autoimmune, subepidermal, blistering skin disease. To our knowledge, this is the 25th documented case of such an association. Following treatment for less than 3 months consisting of methylprednisolone at decreasing dose levels along with four courses of rituximab (monoclonal antibody directed against the CD20 protein), AHA was completely cured and BP well-controlled.Conclusions. This report illustrates a rare association of AHA and BP, supporting the possibility of eradicating the inhibitor with a well-conducted short-term treatment.

scholarly journals Persistent surgical wound bleeding: A rare condition related to acquired hemophilia A

2013 ◽  
Vol 46 (4) ◽  
pp. 135-139
Author(s):  
Chia-Wei Chang ◽  
Jiun-Ting Yeh ◽  
Shang-Yu Wang ◽  
Chun-Hsiang Ouyang ◽  
Chien-Hung Liao ◽  
...  
Keyword(s):  
Hemophilia A ◽  
Rare Condition ◽  
Surgical Wound ◽  
Acquired Hemophilia A ◽  
Acquired Hemophilia

Two Cases of Acquired Hemophilia A Successfully Treated with Oral Steroid or Danazol

2005 ◽  
Vol 40 (1) ◽  
pp. 58 ◽  
Author(s):  
Sun Young Park ◽  
Jin Seok Kim ◽  
Yuri Kim ◽  
In Hae Park ◽  
June-Won Cheong ◽  
...  
Keyword(s):  
Hemophilia A ◽  
Oral Steroid ◽  
Acquired Hemophilia A ◽  
Acquired Hemophilia

scholarly journals The First Case of Postpartum Acquired Hemophilia A in Korea

2011 ◽  
Vol 26 (9) ◽  
pp. 1247 ◽  
Author(s):  
Ji Hyun Lee ◽  
Dong-Hwan Kim ◽  
Kiyoung Yoo ◽  
Yongmook Choi ◽  
Sun-Hee Kim ◽  
...  
Keyword(s):  
Hemophilia A ◽  
Acquired Hemophilia A ◽  
Acquired Hemophilia ◽  
First Case
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