一例疑似罕见血型B(A)型的患者。

IF 0.6 Q4 HEMATOLOGY Asian Journal of Transfusion Science Pub Date : 2024-07-01 Epub Date: 2022-09-28 DOI:10.4103/ajts.ajts_166_21
Avineesh Chandra, P M Bala Bhasker, Romesh Jain, Rakesh Kumar, Subodh Srivastava
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引用次数: 0

摘要

20世纪初,Karl Landsteiner发现了ABO血型系统,但在检测ABO亚群或较弱变异时,免疫血液学仍然存在不确定性。患者样本中弱亚群的存在导致正向(细胞)和反向(血清)分组的差异。我们在此报告一例B(a)表型的患者谁被诊断为慢性肝病急性胰腺炎,需要包装红细胞由于贫血。采用血清学检测和吸附洗脱技术解决血型差异。管法血组与抗a抗血清凝集2+,与抗B、抗ab、抗d抗血清强凝集(4+),与A1细胞凝集4+,与B、O细胞无凝集。洗脱和最后一次洗涤的结果对所有使用的供体细胞都是阴性的。本报告强调了细胞和血清分组、解决血型差异以及及时提供交叉配型相容血液成分的重要性。这种罕见的表型是印度首次报道的。
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A patient with probable rare blood Group B(A) phenotype.

Karl Landsteiner discovered ABO blood group system in the early 20th century, but still, uncertainty remains in immunohematology while detection of ABO subgroups or weaker variants. The presence of weak subgroups in patient samples gives rise to the discrepancy in forward (cell) and reverse (serum) grouping. We here report a case of the B(A) phenotype in a patient who was diagnosed with chronic liver disease with acute pancreatitis, requiring packed red blood cells due to anemia. The blood group discrepancy was resolved using serological testing and adsorption-elution technique. Blood grouping by the tube technique showed 2+ agglutination with anti-A antisera, strong agglutination (4+) with anti-B, anti-AB, and anti-D antisera, 4+ agglutination with A1 cells, and no agglutination with B cells and O cells in serum grouping. Results for both eluate and last wash were negative to all the donor cells used. This report highlights the importance of cell and serum grouping, solving blood group discrepancy, and also in providing crossmatch compatible blood components without delay. This rare phenotype in a patient is the first of its kind reported from India.

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来源期刊
CiteScore
0.90
自引率
0.00%
发文量
56
审稿时长
44 weeks
期刊最新文献
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