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抗赖特(抗Wra)所致新生儿溶血病:病例报告及文献复习

Hemolytic disease of the newborn caused by anti-Wright (anti-Wra): case report and review of literature.

作者信息

Squires Amanda, Nasef Nehad, Lin Yulia, Callum Jeannie, Khadawardi Emad M, Drolet Christine, Core David, Simmons Brian

机构信息

NICU at Sunnybrook Health Sciences Center, Toronto, Canada.

出版信息

Neonatal Netw. 2012 Mar-Apr;31(2):69-80. doi: 10.1891/0730-0832.31.2.69.

DOI:10.1891/0730-0832.31.2.69
PMID:22397791
Abstract

Antibodies to red cell antigens that are found at low frequency in the general population are rare causes of hemolytic disease of the newborn. To understand how to detect these cases, we provide a basic review of routine antenatal maternal antibody testing and report a case of a neonate with severe HDN caused by anti-Wright (anti-Wra), successfully managed with transfusion, phototherapy, and high-dose intravenous immunoglobulin. When hemolysis in a newborn is suspected in the absence of major blood group incompatibility or commonly detected maternal red cell antibodies, a direct antiglobulin test should be performed. A positive DAT should alert the clinician to the presence of maternal antibodies against low-incidence antigens. Antibodies to the Wra antigen are one such rare cause of HDN.

摘要

针对在普通人群中低频出现的红细胞抗原的抗体,是新生儿溶血病的罕见病因。为了解如何检测这些病例,我们对常规产前母体抗体检测进行了基本回顾,并报告了一例由抗赖特(抗-Wra)引起的严重新生儿溶血病病例,该病例通过输血、光疗和大剂量静脉注射免疫球蛋白成功得到治疗。当怀疑新生儿发生溶血但不存在主要血型不相容或常见的母体红细胞抗体时,应进行直接抗球蛋白试验。直接抗球蛋白试验阳性应提醒临床医生存在针对低发生率抗原的母体抗体。抗Wra抗原的抗体就是导致新生儿溶血病的此类罕见病因之一。

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Hemolytic disease of the newborn caused by anti-Wright (anti-Wra): case report and review of literature.抗赖特(抗Wra)所致新生儿溶血病:病例报告及文献复习
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引用本文的文献

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Alloimmunization to low and high prevalence blood group antigens: rare causes of hemolytic disease of the fetus and newborn.对低频率和高频率血型抗原的同种免疫:胎儿和新生儿溶血病的罕见病因。
J Perinatol. 2025 Feb;45(2):287-290. doi: 10.1038/s41372-024-02186-w. Epub 2024 Dec 7.
2
Fatal Acute Hemolytic Transfusion Reaction due to Anti-Wr.抗Wr导致的致命性急性溶血性输血反应
Transfus Med Hemother. 2018 Nov;45(6):438-441. doi: 10.1159/000488863. Epub 2018 Aug 24.