Literature DB >> 1173173

Childhood idiopathic thrombocytopenic purpura. Aggressive management of life-threatening complications.

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:  

Mesh:

Substances:

Year:  1975        PMID: 1173173

Source DB:  PubMed          Journal:  JAMA        ISSN: 0098-7484            Impact factor:   56.272


  3 in total

Review 1.  Intracranial haemorrhage in idiopathic thrombocytopenic purpura. Paediatric Haematology Forum of the British Society for Haematology.

Authors:  J S Lilleyman
Journal:  Arch Dis Child       Date:  1994-09       Impact factor: 3.791

2.  [Vincristin-therapy of chronic refractory idiopathic thrombocytopenic purpura (author's transl)].

Authors:  G Zeile
Journal:  Blut       Date:  1978-04-20

3.  Therapeutic Suggestions for Chronic Subdural Hematoma Associated with Idiopathic Thrombocytopenic Purpura: A Case Report and Literature Review.

Authors:  Hajime Takase; Junya Tatezuki; Naoki Ikegaya; Daisuke Yamamoto; Mizuki Hashimoto; Makoto Takagi; Yasuhiko Mochimatsu; Nobutaka Kawahara
Journal:  NMC Case Rep J       Date:  2015-06-26
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.