Childhood Idiopathic Thrombocytopenic Purpura
- 19 May 1975
- journal article
- research article
- Published by American Medical Association (AMA)
- Vol. 232 (7) , 734-736
- https://doi.org/10.1001/jama.1975.03250070030019
Abstract
Idiopathic thrombocytopenic purpura (ITP) in childhood is usually a benign, self-limited illness. Life-threatening complications, such as central nervous system (CNS) hemorrhage, occur in less than 1% of cases. We report a case in which the patient failed to respond to splenectomy and highdose corticosteroid therapy. Immunosupressive therapy with cyclophosphamide, vincristine sulfate, and corticosteroids in conjunction with frequent transfusions of platelets was associated with a complete remission that persisted after therapy was discontinued. (JAMA232:734-737, 1975)Keywords
This publication has 3 references indexed in Scilit:
- Stimulation of Nonimmunized Lymphocytes by Platelet-Antibody Complexes in Idiopathic Thrombocytopenic PurpuraNew England Journal of Medicine, 1973
- Idiopathic thrombocytopenic purpura: An epidemiologic studyThe Journal of Pediatrics, 1973
- Studies on the Suppression of Immune Responses by the Periwinkle Alkaloids Vincristine and Vinblastine*Journal of Clinical Investigation, 1964