镰状细胞病母亲因轻微血型同种异体免疫而导致胎儿和新生儿溶血病。

IF 0.6 Q4 HEMATOLOGY
Asian Journal of Transfusion Science Pub Date : 2023-07-01 Epub Date: 2023-05-11 DOI:10.4103/ajts.ajts_161_22
Stephy Varghese, Satya Prakash, Somnath Mukherjee, Ansuman Sahu, Debasish Mishra
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引用次数: 0

摘要

胎儿和新生儿溶血病是由于母体 IgG 抗体通过胎盘转运并破坏新生儿红细胞所致。母体和胎儿之间的抗原不匹配会导致同种免疫,从而引起轻度贫血,在宫内可能发展为胎儿水肿,在新生儿中可能发展为严重的高胆红素血症和新生儿红细胞症。同种免疫主要由 Rh-D 和 ABO 抗体引起。在本病例报告中,我们发现新生儿高胆红素血症是由于镰状细胞病(SCD)孕妇体内存在抗异体抗体所致。在需要交换输血的 SCD 患者中,因轻微血型同种异体免疫而导致胎儿高胆红素血症的病例并不多见。应告知多次输血的患者,为了更好地治疗母婴,需要在怀孕前经常进行抗体筛查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hemolytic disease of the fetus and newborn due to minor blood group alloimmunization in a mother of sickle cell disease with multiple alloantibodies.

Hemolytic disease of the fetus and newborn is due to maternal IgG antibodies that transport through the placenta and destroy neonatal red cells. A mismatch of antigens between mother and fetus causes isoimmunization resulting in mild anemia, which may progress to fetal hydrops in the intrauterine period and severe hyperbilirubinemia to kernicterus in neonates. The isoimmunization is mainly caused by Rh-D and ABO antibodies. In this case report, we found neonatal hyperbilirubinemia due to the presence of anti-c alloantibody previously developed in a sickle cell disease (SCD) pregnant female. It is an unusual case of fetal hyperbilirubinemia due to minor blood group alloimmunization in a SCD needing exchange transfusion. Multi-transfused patients should be counseled regarding the need to perform antibody screening frequently before pregnancy for better treatment of both mother and child.

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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
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