High-Dose Intravenous Immunoglobulin for Post-Transfusion Purpura
- 3 February 1983
- journal article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 308 (5), 287
- https://doi.org/10.1056/nejm198302033080526
Abstract
To the Editor: Intravenous immunoglobulin has recently been shown to be effective in treating autoimmune thrombocytopenia (May 27 issue)1 , 2 and autoimmune neutropenia (July 22 issue).3 Another rare but well-defined, immunologically mediated thrombocytopenia is the syndrome of post-transfusion purpura,4 approximately 40 to 50 cases of which have been documented. Thrombocytopenia is usually persistent, and bleeding can be life-threatening. Plasma exchange may be effective, but no other mode of treatment is of established value.5 We recently observed a case of documented post-transfusion purpura in which intravenous immunoglobulin immediately reversed the thrombocytopenia.The patient, a 36-year-old white woman, presented in March 1981 with . . .Keywords
This publication has 4 references indexed in Scilit:
- Identification by HLA Typing of Intrauterine-Derived Maternal T Cells in Four Patients with Severe Combined ImmunodeficiencyNew England Journal of Medicine, 1982
- Transient Reversal of Thrombocytopenia in Idiopathic Thrombocytopenic Purpura by High-Dose Intravenous Gamma GlobulinNew England Journal of Medicine, 1982
- HIGH-DOSE INTRAVENOUS GAMMAGLOBULIN FOR IDIOPATHIC THROMBOCYTOPENIC PURPURA IN CHILDHOODThe Lancet, 1981
- IMMUNOREACTIONS INVOLVING PLATELETS. V. POST-TRANSFUSION PURPURA DUE TO A COMPLEMENT-FIXING ANTIBODY AGAINST A GENETICALLY CONTROLLED PLATELET ANTIGEN. A PROPOSED MECHANISM FOR THROMBOCYTOPENIA AND ITS RELEVANCE IN “AUTOIMMUNITY”*Journal of Clinical Investigation, 1961