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慢性特发性血小板减少性紫癜(ITP):环磷酰胺治疗后发生急性非淋巴细胞白血病。

Chronic idiopathic thrombocytopenic purpura (ITP:) development of acute non-lymphocytic leukemia subsequent to treatment with cyclophosphamide.

作者信息

Krause J R

出版信息

Med Pediatr Oncol. 1982;10(1):61-5. doi: 10.1002/mpo.2950100110.

DOI:10.1002/mpo.2950100110
PMID:7199614
Abstract

Chronic idiopathic thrombocytopenic purpura (ITP) is most often treated successfully with steroids and/or splenectomy. In those who fail to respond with the foregoing treatment, immunosuppressive drugs are sometimes added to the regimen. Cyclophosphamide has been reported heretofore to be effective with a minimum of side effects and complications. However, the use of alkylating agents and the induction of a second malignancy is now well recognized. This report describes three cases of refractory ITP treated with cyclophosphamide who subsequently developed an acute non-lymphocytic leukemia. Cyclophosphamide should be used with discretion in the treatment of chronic idiopathic thrombocytopenic purpura which is a non-neoplastic disorder.

摘要

慢性特发性血小板减少性紫癜(ITP)通常使用类固醇和/或脾切除术成功治疗。对于那些对上述治疗无反应的患者,有时会在治疗方案中添加免疫抑制药物。迄今为止,据报道环磷酰胺有效且副作用和并发症最少。然而,现在人们已经充分认识到使用烷化剂会诱发第二种恶性肿瘤。本报告描述了三例用环磷酰胺治疗的难治性ITP患者,这些患者随后发展为急性非淋巴细胞白血病。在治疗作为一种非肿瘤性疾病的慢性特发性血小板减少性紫癜时,应谨慎使用环磷酰胺。

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Chronic idiopathic thrombocytopenic purpura (ITP:) development of acute non-lymphocytic leukemia subsequent to treatment with cyclophosphamide.慢性特发性血小板减少性紫癜(ITP):环磷酰胺治疗后发生急性非淋巴细胞白血病。
Med Pediatr Oncol. 1982;10(1):61-5. doi: 10.1002/mpo.2950100110.
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Acute nonlymphocytic leukemia after cyclophosphamide therapy for refractory idiopathic thrombocytopenic purpura.环磷酰胺治疗难治性特发性血小板减少性紫癜后发生的急性非淋巴细胞白血病。
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J Korean Med Sci. 2008 Jun;23(3):445-51. doi: 10.3346/jkms.2008.23.3.445.
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Current concepts in the treatment of immune thrombocytopenia.
Drugs. 1990 Oct;40(4):531-42. doi: 10.2165/00003495-199040040-00004.
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Guidelines for management of idiopathic thrombocytopenic purpura. The British Paediatric Haematology Group.特发性血小板减少性紫癜管理指南。英国儿科学血液学组。
Arch Dis Child. 1992 Aug;67(8):1056-8. doi: 10.1136/adc.67.8.1056.