Refractory Idiopathic Thrombocytopenic Purpura
- 1 May 1980
- journal article
- Published by American College of Physicians in Annals of Internal Medicine
- Vol. 92 (5) , 713-714
- https://doi.org/10.7326/0003-4819-92-5-713_2
Abstract
To the editor: Most patients with idiopathic thrombocytopenic purpura have sustained remissions after splenectomy. Most patients with persistent thrombocytopenia after splenectomy respond to steroids, cytotoxic agents, or vinca alkaloids when given as single agents (1-3). This report describes a case of refractory idiopathic thrombocytopenic purpura that did not respond to single-agent therapy but did respond to combination therapy with vinblastine infusions plus cyclophosphamide and prednisone. A 43-year-old Japanese-American woman presented in February 1979 with easy bruising. She had been taking hydrochlorothiazide for mild hypertension. Physical examination revealed only petechiae and bruises. Hemoglobin level was 14.1 g/dL, hematocrit 40%, leukocyte countThis publication has 5 references indexed in Scilit:
- The Treatment of Idiopathic Thrombocytopenia with Vinblastine-Loaded PlateletsNew England Journal of Medicine, 1978
- Treatment of Idiopathic Thrombocytopenic Purpura (ITP)Annual Review of Medicine, 1977
- Vincristine for Treatment of Refractory Autoimmune ThrombocytopeniaNew England Journal of Medicine, 1976
- Treatment of refractory thrombocytopenic purpura with cyclophosphamideAmerican Journal of Hematology, 1976
- Quantitative Determination of Antibody in Idiopathic Thrombocytopenic PurpuraNew England Journal of Medicine, 1975