Neonatal testing leading to the identification of Bh (para-Bombay) phenotype in the mother: case report with review of the literature.

Q4 Medicine
G Mohan, A Vaidya, S Shastry
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引用次数: 0

Abstract

Para-Bombay is a rare phenotype with a homozygous nonfunctional FUT1 gene and a normal FUT2 gene leading to H-deficient red blood cells (RBCs) with or without ABH substances, depending on inheritance of the ABO gene. This case is about a 5-day-old male baby suffering from sepsis who required a 45-mL packed RBC transfusion. The baby's sample tested as A1B, D+ and mother's sample tested as group O, D+ with group 4 discrepancy due to ABO isoagglutinins. Further workup of the mother's sample with anti-H lectin was negative, which suggested the mother to be group Oh, D+. Antibody screening was panreactive with negative autocontrol, suggestive of anti-H. The titer of immunoglobulin (Ig)M anti-H was 64, IgG titer using dithiothreitol was 8, and anti-IH was absent. A negative adsorption and elution test suggested that RBCs were devoid of A and B antigens. The father's sample tested clearly as group A1, D+; hence, the cis-AB blood group was ruled out in the baby. The secretor study of the mother's saliva revealed the presence of B and H substances that neutralized polyclonal B and H antisera. Therefore, we concluded that the mother was of the para-Bombay (Bh) phenotype. This case highlights the importance of reverse grouping and resolving blood grouping discrepancies between mother and child-in this case because of an incongruous ABO blood type of the baby and the mother who was previously tested as group O, D+.

Para-Bombay is a rare phenotype with a homozygous nonfunctional FUT1 gene and a normal FUT2 gene leading to H-deficient red blood cells (RBCs) with or without ABH substances, depending on inheritance of the ABO gene. This case is about a 5-day-old male baby suffering from sepsis who required a 45-mL packed RBC transfusion. The baby’s sample tested as A1B, D+ and mother’s sample tested as group O, D+ with group 4 discrepancy due to ABO isoagglutinins. Further workup of the mother’s sample with anti-H lectin was negative, which suggested the mother to be group Oh, D+. Antibody screening was panreactive with negative autocontrol, suggestive of anti-H. The titer of immunoglobulin (Ig)M anti-H was 64, IgG titer using dithiothreitol was 8, and anti-IH was absent. A negative adsorption and elution test suggested that RBCs were devoid of A and B antigens. The father’s sample tested clearly as group A1, D+; hence, the cis-AB blood group was ruled out in the baby. The secretor study of the mother’s saliva revealed the presence of B and H substances that neutralized polyclonal B and H antisera. Therefore, we concluded that the mother was of the para-Bombay (Bh) phenotype. This case highlights the importance of reverse grouping and resolving blood grouping discrepancies between mother and child―in this case because of an incongruous ABO blood type of the baby and the mother who was previously tested as group O, D+.

新生儿测试导致鉴定Bh(类孟买)表型在母亲:病例报告与文献回顾。
Para-Bombay是一种罕见的表型,具有纯合的无功能FUT1基因和正常的FUT2基因,导致h缺乏性红细胞(rbc)是否含有ABH物质,这取决于ABO基因的遗传。这个病例是一个5天大的男婴,患有败血症,需要45毫升的红细胞输血。由于ABO异凝集素的原因,婴儿样本检测为A1B, D+,母亲样本检测为O, D+,存在4组差异。进一步对母亲样本进行抗h凝集素检测为阴性,提示母亲为Oh, D+组。抗体筛选呈全反应性,自控阴性,提示抗h。免疫球蛋白(Ig)M抗h滴度为64,二硫苏糖醇IgG滴度为8,无抗ih。吸附和洗脱试验阴性提示红细胞缺乏A和B抗原。父亲样本检测结果明显为A1、D+组;因此,该婴儿排除了顺式ab血型。母亲唾液分泌研究显示存在B和H物质,可中和多克隆B和H抗血清。因此,我们得出结论,母亲是准孟买(Bh)表型。这个病例强调了反向分组和解决母亲和孩子之间血型差异的重要性——在这个病例中,由于婴儿的ABO血型与先前检测为O, D+组的母亲不一致。Para-Bombay是一种罕见的表型,具有纯合的无功能FUT1基因和正常的FUT2基因,导致h缺乏性红细胞(rbc)是否含有ABH物质,这取决于ABO基因的遗传。这个病例是一个5天大的男婴,患有败血症,需要45毫升的红细胞输血。由于ABO异凝集素的原因,婴儿样本检测为A1B, D+,母亲样本检测为O, D+,存在4组差异。进一步对母亲样本进行抗h凝集素检测为阴性,提示母亲为Oh, D+组。抗体筛选呈全反应性,自控阴性,提示抗h。免疫球蛋白(Ig)M抗h滴度为64,二硫苏糖醇IgG滴度为8,无抗ih。吸附和洗脱试验阴性提示红细胞缺乏A和B抗原。父亲样本检测结果明显为A1、D+组;因此,该婴儿排除了顺式ab血型。母亲唾液分泌研究显示存在B和H物质,可中和多克隆B和H抗血清。因此,我们得出结论,母亲是准孟买(Bh)表型。这个病例强调了反向分组和解决母亲和孩子之间血型差异的重要性——在这个病例中,由于婴儿的ABO血型与先前检测为O, D+组的母亲不一致。
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
Immunohematology
Immunohematology Medicine-Medicine (all)
CiteScore
1.30
自引率
0.00%
发文量
18
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