| Literature DB >> 1173173 |
A L Lightsey, R McMillan, H M Koenig.
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 high-dose corticosteroid therapy. Immunosuppressive 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.Entities:
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Year: 1975 PMID: 1173173
Source DB: PubMed Journal: JAMA ISSN: 0098-7484 Impact factor: 56.272