青少年不明原因的细胞减少症?你想想看。

Justin Rueckert, Heather Bradeen, Katherine Devitt, Juli-Anne Gardner
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引用次数: 0

摘要

目的:DNA结合蛋白GATA家族由六种不同的转录因子(GATA1-6)组成,每种转录因子都具有不同的生物学功能。转录因子GATA1-3的功能主要是协调造血;然而,它们在非造血细胞中也有作用。我们目前对GATA转录因子的大部分知识来自于对已知GATA突变的疾病状态的观察。GATA2蛋白已被证明对造血干细胞的增殖和维持至关重要;突变导致包括骨髓增生异常综合征在内的各种表型。我们报告一个19岁的男性病例,他有全血细胞减少和骨髓细胞减少的历史,并伴有发育不良的形态学改变,他接受了广泛的检查以确定病因。分子鉴定鉴定出一株种系GATA2 c.1081C>T杂合突变,使该病例被归类为世界卫生组织(WHO)实体:髓系肿瘤伴种系GATA2突变。
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Unexplained cytopenias in an adolescent? You GATA think about it.

Objectives: The GATA family of DNA binding proteins consists of six different transcription factors (GATA1-6), each with a diverse biologic function. The transcription factors GATA1-3 function primarily to orchestrate hematopoiesis; however, they have roles in non-hematopoietic cells as well. Much of our current knowledge of the GATA transcription factors has come through observation of disease states with known GATA mutations. The GATA2 protein has been shown to be vital for proliferation and maintenance of hematopoietic stem cells; mutations result in variable phenotypes including myelodysplastic syndrome. We present a case of a 19-year-old male with a history of pancytopenia and hypocellular bone marrow with dysplastic morphologic changes who underwent an extensive workup to determine an etiology. Molecular testing identified a germline GATA2 c.1081 C>T heterozygous mutation, allowing his case to be classified as the World Health Organization (WHO) entity: myeloid neoplasm with germline GATA2 mutation.

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