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获得性再生障碍性贫血中因杂合性拷贝数中性缺失导致的假纯合HLA基因分型结果

False homozygous HLA genotyping results due to copy number neutral loss of heterozygosity in acquired aplastic anaemia.

作者信息

Heyrman Bert, De Becker Ann, Verheyden Sonja, Demanet Christian

机构信息

Department of Hematology, Universitair Ziekenhuis Brussels, Brussels, Belgium.

Department of Molecular Hematology, Universitair Ziekenhuis Brussels, Brussels, Belgium.

出版信息

BMJ Case Rep. 2017 Mar 2;2017:bcr2016217867. doi: 10.1136/bcr-2016-217867.

Abstract

The aim of this case report is to draw attention on possible false human leucocyte antigen (HLA) genotyping in acquired aplastic anaemia prior to allogeneic haematopoietic stem cell transplantation. In acquired aplastic anaemia loss of heterozygosity (LOH) of chromosome 6p is known to occur in around 12%. We report false HLA genotyping results due to LOH and a coinciding steep rise in neutrophils following filgrastim stimulation in a patient with very severe aplastic anaemia. At diagnosis we obtained heterozygous results on peripheral blood. Failing to reach a partial response at 6 months with immune-suppressive therapy we repeated HLA genotyping, obtaining homozygous results. Repeated testing confirmed loss of HLA genotype heterozygosity. HLA genotyping on cells obtained by a buccal swab confirmed the previous HLA heterozygosity. A second course of filgrastim at the time of homozygous HLA genotyping resulted in a steep rise in neutrophils. Stopping filgrastim resulted in an equally steep drop.

摘要

本病例报告的目的是引起人们对异基因造血干细胞移植前获得性再生障碍性贫血中可能出现的人类白细胞抗原(HLA)基因分型错误的关注。在获得性再生障碍性贫血中,已知6号染色体短臂杂合性缺失(LOH)的发生率约为12%。我们报告了1例极重型再生障碍性贫血患者因LOH导致的HLA基因分型结果错误,以及在使用非格司亭刺激后中性粒细胞同时急剧上升的情况。诊断时,我们在外周血中获得了杂合结果。免疫抑制治疗6个月未能达到部分缓解,我们重复进行HLA基因分型,得到了纯合结果。重复检测证实了HLA基因型杂合性的丧失。通过口腔拭子获取的细胞进行的HLA基因分型证实了先前的HLA杂合性。在HLA基因分型为纯合时再次使用非格司亭导致中性粒细胞急剧上升。停用非格司亭导致同样急剧下降。

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