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首页> 外文期刊>Turkish Journal of Hematology >Immune Thrombocytopenic Purpura During Maintenance Phase of Acute Lymphoblastic Leukemia: A Rare Coexistence Requiring a High Degree of Suspicion, a Case Report and Review of the Literature
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Immune Thrombocytopenic Purpura During Maintenance Phase of Acute Lymphoblastic Leukemia: A Rare Coexistence Requiring a High Degree of Suspicion, a Case Report and Review of the Literature

机译:急性淋巴细胞白血病维持期的免疫性血小板减少性紫癜:罕见的共存,需要高度怀疑,一例病例并文献复习

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Thrombocytopenia may develop in patients with acute lymphoblastic leukemia (ALL) due to myelosuppression ofchemotherapy or relapse. Here we report a pediatric patient with ALL whose platelet counts decreased at the 102ndweek of maintenance treatment. Thrombocytopenia was refractory to platelet infusions and bone marrow aspirationrevealed remission status for ALL along with increased megakaryocytes. The cessation of chemotherapy for 2 weekscaused no increase in thrombocyte counts. The viral serology was unrevealing. A diagnosis of immune thrombocytopenicpurpura (ITP) was established. After administration of intravenous immunoglobulin, the thrombocytopenia resolved.When thrombocytopenia occurs in patients with ALL in remission, ITP should be kept in mind after exclusion of themore common etiologies.
机译:急性淋巴细胞白血病(ALL)患者可能由于骨髓抑制化疗或复发而导致血小板减少。在这里,我们报告了一名小儿ALL患者,其维持治疗的第102周血小板计数下降。血小板减少症对血小板输注和骨髓抽吸的缓解状态均不利,同时巨核细胞增多。停止化疗2周不会导致血小板计数增加。病毒血清学未发现。建立了免疫性血小板减少性紫癜(ITP)的诊断。静脉注射免疫球蛋白后,血小板减少症得以缓解。当ALL缓解的患者发生血小板减少症时,应排除更常见的病因后应注意ITP。

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