Challenges in blood transfusion caused by anti-Hr0: A rare case of D-- Phenotype in Asia Abstract

IF 1.2 Q4 GENETICS & HEREDITY
Yuanyuan Luo, Chunya Ma, Lihui Fu, Yang Yu
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引用次数: 0

Abstract

D–Phenotype is linked to abnormal expression of RHCE gene. Consequently, individuals with this condition may develop antibodies against high-prevalence Rh antigens when exposed to a normal Rh phenotype, leading to challenges in blood matching. A 90-year-old male was admitted to the hospital due to prostatitis and acute retention of urinary. Surgery was planned after evaluation by urologist. A request was made for 2 units of red blood cells (RBC). The result for unexpected antibody screening was positive, and the antibody was identified as anti-Hr0 alloantibody , a rare RHCE * CE-D (5) – CE was discovered by genetic testing. The patient has only one history of blood transfusion, which may result in the production of the anti-Hr0 antibody. Compatible blood donors for this patient were not found, even after extensive screening. This report records a rare case of a D-- phenotype individual who produced anti-Hr0 alloantibody. Subsequent analysis of RH gene sequencing revealed a genotype that has not been previously reported in Asia.
抗Hr0给输血带来的挑战:亚洲一例罕见的D--表型病例 摘要
D 表型与 RHCE 基因的异常表达有关。因此,患有这种病症的人在接触正常的 Rh 表型时,可能会产生针对高流行率 Rh 抗原的抗体,从而导致血液配对方面的挑战。一名 90 岁的男性因前列腺炎和急性尿潴留入院。经泌尿科医生评估后,计划进行手术治疗。患者需要 2 个单位的红细胞(RBC)。意外的抗体筛查结果呈阳性,抗体被确定为抗 Hr0 同种抗体,这是一种通过基因检测发现的罕见 RHCE * CE-D (5) - CE。患者只有一次输血史,这可能会导致抗 Hr0 抗体的产生。即使经过广泛筛查,也没有找到与该患者匹配的献血者。本报告记录了一例罕见的 D--表型个体产生抗 Hr0 同种抗体的病例。随后的 RH 基因测序分析表明,这种基因型以前在亚洲从未报道过。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Egyptian Journal of Medical Human Genetics
Egyptian Journal of Medical Human Genetics Medicine-Genetics (clinical)
CiteScore
2.20
自引率
7.70%
发文量
150
审稿时长
18 weeks
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