Post-transfusion purpura in a patient with HPA-1a and GPIa/IIa antibodies.
Transfus Med
; 16(1): 69-72, 2006 Feb.
Article
in En
| MEDLINE
| ID: mdl-16480442
ABSTRACT
Post-transfusion purpura is a rare bleeding disorder characterized by severe and sudden thrombocytopenia within 3-12 days after blood transfusion. Typically, preformed antibodies directed against human platelet antigens, especially HPA-1a, are associated with the clinical symptoms. A 46-year-old female presenting to the hospital with acute progressive kidney insufficiency and anaemia received two units of packed red blood cells (RBC) within 2 days. On day 7, platelet count felt from 414 to 189 x 10(9) L(-1) and 1 day later dropped to 4 x 10(9) L(-1). Four platelet concentrates were applied without success. After serological confirmation of an HPA-1a antibody, the patient was treated with intravenous gamma immunoglobulin (ivIgG), and the platelet count increased to normal values on day 17. In addition to the persisting HPA-1a alloantibody, an antibody reactive with GPIa/IIa of HPA-5a- and HPA-5b-positive platelets was detected during the acute phase of thrombocytopenia. After complete remission, the patient was transfused with four units of packed RBC from HPA-1a-negative donors, and platelet counts remained normal.
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Purpura
/
Antigens, Human Platelet
/
Integrin alpha2beta1
/
Transfusion Reaction
/
Isoantibodies
Type of study:
Diagnostic_studies
/
Etiology_studies
Limits:
Female
/
Humans
/
Middle aged
Language:
En
Journal:
Transfus Med
Year:
2006
Document type:
Article