儿童患者免疫性血小板减少症与t淋巴母细胞淋巴瘤的关系。

IF 0.7 Q4 HEMATOLOGY
Case Reports in Hematology Pub Date : 2019-12-17 eCollection Date: 2019-01-01 DOI:10.1155/2019/1425151
Ryan A Denu, Daniel R Matson, Matthew J Davis, Natalie J Tedford, Christine E Brichta, Carol A Diamond, Margo L Hoover-Regan
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引用次数: 1

摘要

免疫性血小板减少症(ITP)以病因不明的孤立性血小板减少为特征。我们提出一个独特的案例,一个8岁的女孩慢性ITP谁随后被诊断为t淋巴母细胞淋巴瘤在11岁。在给予奈拉宾、鞘内注射和大剂量全身甲氨蝶呤后,临床过程因非癫痫样事件的发生和奇怪的行为改变而复杂化。本病例强调了一个不寻常的血液恶性肿瘤和慢性ITP在其他健康的儿童共同发生。我们推测,潜在的遗传或免疫病变可能使一部分儿童ITP患者易患血液系统恶性肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Association of Immune Thrombocytopenia and T-Lymphoblastic Lymphoma in a Pediatric Patient.

Association of Immune Thrombocytopenia and T-Lymphoblastic Lymphoma in a Pediatric Patient.

Association of Immune Thrombocytopenia and T-Lymphoblastic Lymphoma in a Pediatric Patient.

Immune thrombocytopenia (ITP) is characterized by isolated thrombocytopenia of unclear etiology. We present a unique case of an 8-year-old girl with chronic ITP who was subsequently diagnosed with T-lymphoblastic lymphoma at age 11. The clinical course was complicated by the occurrence of nonepileptiform events with bizarre behavior changes following the administration of nelarabine and intrathecal and high-dose systemic methotrexate. This case highlights an unusual co-occurrence of hematologic malignancy and chronic ITP in an otherwise healthy child. We speculate that underlying genetic or immunologic lesions may predispose a subset of pediatric ITP patients to the development of hematologic malignancies.

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