Volume 5, Issue 3 (Autumn 2013 2013)
2013, 5(3): 673-675 |
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Tabarai M, Mohamaddoust H, Omidvar S. post transfusion purpura: case report. North Khorasan University of Medical Sciences 2013; 5 (3) :673-675
URL: http://journal.nkums.ac.ir/article-1-404-en.html
URL: http://journal.nkums.ac.ir/article-1-404-en.html
Abstract: (5243 Views)
Post-transfusion purpura is a rare immunohematological disorder characterized by severe thrombocytopenia following transfusion of blood components and induced by an alloantibody against a donor platelet antigen. It occurs primarily in women sensitized by pregnancy and is most commonly caused by anti-human platelet antigen-1a antibodies. Here, we describe what we believe to be the first suspicious case of an Iranian woman who developed post-transfusion purpura after receiving multiple blood products
Type of Study: Case Report |
Subject:
Basic Sciences
Received: 2015/03/28 | Accepted: 2015/03/28 | Published: 2015/03/28
Received: 2015/03/28 | Accepted: 2015/03/28 | Published: 2015/03/28
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