ABO discrepancies revealing rare weak A subgroups: a 2-case series.

IF 1
Ande Marchini, Chinelo Onyenekwu, Patricia Ruegsegger, Christine Fuja, William Rose, Caitlin Raymond
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Abstract

Introduction: ABO discrepancies caused by weak A subgroups are uncommon but clinically important because they can lead to mistyping and inappropriate transfusion management.

Methods: We present the cases of 2 patients at an academic medical center who were historically typed as group O but were found to harbor weak A subgroups upon detailed investigation.

Results: In case 1, the patient's red blood cells demonstrated weak reactivity with anti-A reagent on forward typing, with anti-A1 and anti-B identified on reverse typing. In case 2, the patient's red blood cells were nonreactive with anti-A reagent on forward typing but did agglutinate with anti-A,B reagent. Reverse typing showed weak reactivity against A1 and A2 cells, with strong reactivity against B cells, consistent with an anti-A antibody. In both cases, molecular genotyping performed at a reference laboratory returned results consistent with an Aw or Ael allele.

Discussion: These cases illustrate the serologic spectrum of weak A phenotypes, highlight the variable sensitivity of ABO reagents in detecting minimal antigen expression, and underscore the possible utility of molecular characterization when serologic results are ambiguous.

ABO差异揭示罕见的弱A亚群:2例系列。
由弱A亚群引起的ABO差异并不常见,但在临床上很重要,因为它们可能导致分型错误和输血管理不当。方法:我们报告了一个学术医疗中心的2例患者,他们在历史上被分型为O组,但在详细调查后发现有弱A亚组。结果:病例1患者红细胞正向分型抗a试剂反应弱,反向分型可识别抗a1和抗b。在病例2中,患者的红细胞在正向分型时与抗a试剂无反应,但与抗a、B试剂有凝集。反向分型对A1和A2细胞反应性弱,对B细胞反应性强,与抗a抗体一致。在这两种情况下,在参考实验室进行的分子基因分型结果与Aw或Ael等位基因一致。讨论:这些病例说明了弱A表型的血清学谱,强调了ABO试剂在检测最小抗原表达方面的可变敏感性,并强调了当血清学结果不明确时分子表征的可能效用。
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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