21三体、21四体、19三体暂时性骨髓异常1例。

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL
Miku Munakata, Hayato Go, Shun Hiruta, Hirotaka Ichikawa, Hajime Maeda, Kei Ogasawara, Shingo Kudo, Yoshihiro Ohara, Mitsuaki Hosoya
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引用次数: 0

摘要

背景:短暂性异常骨髓生成(TAM)是一种短暂性异常类白血病反应,发生在大约5-10%的唐氏综合征病例中。TAM通常是自限性的,然而,由于严重的肺部或肝脏并发症,它可能危及生命。大约20%的患者在4岁时病情缓解后发展为急性巨核母细胞白血病。在此,我们报告一例TAM合并21三体、21四体和19三体。病例报告:患者为1日龄男性新生儿,孕16周胎儿超声检查颈透明。由于他出生时的面部特征,他被怀疑患有唐氏综合症。确诊TAM时外周血g带染色显示21三体、21四体、19三体。细胞在4个月大时从外周血中消失。爆炸消失时外周血g带染色显示21四体和19三体消失。结论:从病程推断,21四体和19三体细胞可能为TAM胚细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case of transient abnormal myelopoiesis with trisomy 21, tetrasomy 21, and trisomy 19.

Background: Transient abnormal myelopoiesis (TAM) is a transient abnormal leukemoid reaction that occurs in approximately 5-10% of Down syndrome cases. TAM is typically self-limiting, however, it can be life-threatening because of severe pulmonary or hepatic complications. Approximately 20% of these patients develop acute megakaryoblastic leukemia after remission by the age of 4 years. Here, we report a case of TAM with trisomy 21, tetrasomy 21, and trisomy 19.

Case report: The patient was a 1-day-old male neonate with nuchal translucency measured by fetal ultrasonography at 16 weeks of gestation. He was suspected to have Down syndrome due to his characteristic facial appearance at birth. G-band staining of the peripheral blood when TAM was diagnosed showed trisomy 21, tetrasomy 21, and trisomy 19. The blasts disappeared from the peripheral blood at 4 months of age. G-band staining of the peripheral blood at the time of blast disappearance demonstrated that tetrasomy 21 and trisomy 19 had resolved.

Conclusion: It was inferred from the course of the disease that the cells with tetrasomy 21 and trisomy 19 might be blast cells of TAM.

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来源期刊
Fukushima Journal of Medical Science
Fukushima Journal of Medical Science MEDICINE, GENERAL & INTERNAL-
CiteScore
1.70
自引率
12.50%
发文量
24
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