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伊普西兰蒂血红蛋白病——真性红细胞增多症一种罕见但重要的鉴别诊断。

Haemoglobinopathia Ypsilanti - A rare, but important differential diagnosis to polycythaemia vera.

作者信息

Nygaard Marietta, Petersen Jesper, Bjerrum Ole W

机构信息

Hematological Department, Rigshospitalet, Copenhagen, Denmark.

Hematological Department, Herlev Hospital, Herlev, Denmark.

出版信息

Leuk Res Rep. 2013 Oct 9;2(2):86-8. doi: 10.1016/j.lrr.2013.09.002. eCollection 2013.

Abstract

We present a case of a mother and daughter who were initially diagnosed with polycythaemia vera and treated with venesectio. As JAK2 V6217F/exon 12 mutation analyses became available, these were performed and turned out negative. Haemoglobin electrophoresis was performed and the patients were found to have high oxygen affinity haemoglobin Ypsilanti. It is important and relevant to look for high oxygen affinity variants of haemoglobin when there is a family history of erythrocytosis, in young persons and when there is no apparent reason or clonal marker present.

摘要

我们报告了一例母女病例,她们最初被诊断为真性红细胞增多症并接受了放血治疗。随着JAK2 V6217F/外显子12突变分析技术的出现,对她们进行了检测,结果为阴性。进行了血红蛋白电泳,发现这两名患者患有高氧亲和力血红蛋白伊普西兰蒂。当存在红细胞增多症家族史、患者为年轻人且无明显病因或克隆标志物时,寻找高氧亲和力血红蛋白变体很重要且具有相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fa5/3850385/a266e69cf8c1/gr1.jpg

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