[产妇抗迪致新生儿溶血病(a):台湾1例报告]。

C H Yung, J S Lin, H Y Hu, J Y Lyou, Y R Chen, C R Chen, T C Hao, C S Peng, C H Tzeng
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引用次数: 0

摘要

台湾报道首例可能由抗di (a)引起的新生儿溶血性疾病(HDN)。母亲曾两次怀孕,但没有输血史。她的第一个男婴正常,但她的第二个足月男婴出生后不久出现轻度黄疸,总胆红素水平在24小时,48小时和72小时分别为12.1 mg/dL, 18.3 mg/dL, 23.6 mg/dL。术后第8天总胆红素为9.1 mg/dL。婴儿平静地康复了。免疫血液学检查显示母亲为AB组,Rh (D)+;Di(a - b+),父组为O组,Rh (D)+;男婴Di(a + b+)及其2岁弟弟为b组,Rh(D)+;Di(a + b+)婴儿红细胞直接抗球蛋白试验(DAT)阳性(4+,多特异性AHG;4+抗igg)。母体血清和婴儿红细胞洗脱液常规抗体检测均为阴性,但AHG期手工聚胺试验(MP)和间接抗球蛋白试验(IAT)均含有对抗Di(a+)细胞的同种异体抗体。母亲血清抗Di(a)滴度为mp1∶256,AHG滴度为1:256,婴儿洗脱液抗Di(a + b+)滴度为mp1∶128,AHC滴度为1:64。综合以上结果,我们认为该新生儿黄疸是由母体抗di (a)所致,极有可能是以前妊娠所致。综上所述,迭戈血型是一个具有很高人类学价值的系统,因为它解释了美洲印第安人、日本人和中国人的蒙古人种起源。Anti-Di(a)可能导致HDN,如本例中一位中国婴儿因母体抗- di (a)导致HDN。但在欧洲和美国,几乎所有人都是Di(a - b+)表现型,该系统似乎对父母研究和输血都不感兴趣。由于Di(a)抗原在中国人群中发病率较高,我们建议在台湾的亲代研究和输血中,Diego系统应参与常规相容性检测或抗体鉴定问题。
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 newborn caused by maternal anti-Di(a): a case report in Taiwan].

The first case of hemolytic disease of the newborn (HDN) possibly caused by anti-Di(a) in a Chinese infant in Taiwan is reported. The mother had two pregnancies before but no history of blood transfusion. Her first male infant was normal, but her second full-term male one developed mild jaundice soon after birth, and the total bilirubin level was 12.1 mg/dL, 18.3 mg/dL, 23.6 mg/dL at 24 hours, 48 hours, and 72 hours of age, respectively. Total bilirubin was 9.1 mg/dL on the eighth day after receiving phototherapy and compatible blood exchange transfusion. The infant recovered uneventfully. The immunohematological study revealed that the mother was group AB, Rh (D)+; Di(a - b+), the father was group O, Rh (D)+; Di(a + b+), the infant boy and his 2-year-old brother were group B, Rh(D)+; Di(a + b+). The direct antiglobulin test (DAT) on the infant red cells was positive (4+ with polyspecific AHG; 4+ with anti-IgG). The maternal serum and infant's eluate from red blood cells showed negative reactions in routine antibody detection tests, but they contained alloantibody reacting against the Di(a+) cells by the manual polybrene test (MP) and indirect antiglobulin test (IAT) in AHG phase. The anti-Di(a) titers in the mother's serum was MP 1:256 and AHG 1:256, and in the infant's eluate was MP 1:128 and AHC 1:64 against Di(a + b+) cells. Based on the above results we conclude that the jaundice in this newborn baby was caused by maternal anti-Di(a) which was most likely induced by previous pregnancy. In conclusion, Diego blood group is a system of high value in anthropology because it accounts for the Mongoloid origin of American Indians, Japanese and Chinese. Anti-Di(a) may cause HDN, as in our case of HDN due to maternal anti-Di(a) in a Chinese infant. But in Europe and America, where practically all people are Di(a - b+) phenotypes, the system seems of no interest in parental studies as well as in blood transfusions. Owing to the Di(a) antigen is of higher incidence in Chinese population, we suggest that the Diego system should be involved in routine compatibility testing or antibody identification problems in parental studies and in blood transfusions in Taiwan.

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