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Non-Hodgkin Lymphoma in a Child with Schimke Immuno-Osseous Dysplasia

机译:Schimke免疫性骨发育不良儿童的非霍奇金淋巴瘤

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摘要

Schimke immuno-osseous dysplasia is a rare autosomal recessive multisystem disorder characterized by steroid-resistant nephrotic syndrome, immunodeficiency, and spondyloepiphyseal dysplasia. Mutations in SWI/SNF2 related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 (SMARCAL1) gene are responsible for the disease. The present report describes, for the first time, a Schimke immuno-osseous dysplasia child with SMARCAL1 missense mutation (R561H) and manifestations of intussusception secondary to Epstein-Barr virus-negative non-Hodgkin lymphoma, who expired due to septicemia following chemotherapy. The report emphasizes the necessity of more limited immunosuppressive protocols in Schimke immuno-osseous dysplasia patients with lymphoproliferative disorders.
机译:Schimke免疫性骨发育不良是一种罕见的常染色体隐性遗传性多系统疾病,其特征为类固醇抵抗性肾病综合征,免疫缺陷和脊柱骨赘发育不良。 SWI / SNF2相关的,与基质相关的,肌动蛋白依赖的染色质调节子样亚家族a样1(SMARCAL1)基因突变引起该病。本报告首次描述了具有SMARCAL1错义突变(R561H)和因Epstein-Barr病毒阴性非霍奇金淋巴瘤继发肠套叠的Schimke免疫性骨发育不良儿童,其化疗后因败血症而死亡。该报告强调,对于有淋巴增生性疾病的Schimke免疫性骨发育不良的患者,必须采取更为有限的免疫抑制方案。

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