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慢性特发性血小板减少性紫癜继以慢性粒细胞白血病。

Chronic idiopathic thrombocytopenic purpura followed by chronic myelocytic leukemia.

作者信息

Chu J Y, Gale G B, O'Connor D M, Bouhasin J D, Gallagher N I

出版信息

Am J Pediatr Hematol Oncol. 1981 Spring;3(1):83-5.

PMID:6940461
Abstract

An 8-year old girl was diagnosed as having idiopathic thrombocytopenic purpura which later became refractory to steroids, splenectomy, and immunosuppressive therapy. While she was being treated for pneumococcal meningitis, 7 1/2 years later, she was found to have Philadelphia-chromosome-positive chronic myelocytic leukemia. She died 2 1/2 years after the diagnosis of leukemia. The association of autoimmune disorders and hematologic malignancies has been well-recognized. To our knowledge, there has been no previous report of chronic idiopathic thrombocytopenic purpura preceding the development of chronic myelocytic leukemia in the literature.

摘要

一名8岁女孩被诊断为特发性血小板减少性紫癜,后来对类固醇、脾切除术和免疫抑制治疗均产生耐药。7年半后,她在接受肺炎球菌性脑膜炎治疗时,被发现患有费城染色体阳性的慢性粒细胞白血病。白血病确诊2年半后,她去世了。自身免疫性疾病与血液系统恶性肿瘤之间的关联已得到充分认识。据我们所知,此前文献中尚无慢性特发性血小板减少性紫癜先于慢性粒细胞白血病发生的报道。

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