Ishihara Yuki, Miyata Shigeki, Chiba Yoshihide, Kawai Takeshi
Department of Perinatology, National Cardiovascular Center, Suita, Osaka, Japan.
Fetal Diagn Ther. 2006;21(3):269-71. doi: 10.1159/000091354.
Although Jr(a) hemolytic disease of the newborn (HDN) is generally considered to be mild, we encountered a case of anti-Jr(a) alloimmunization hydrops fetalis due to extremely severe fetal anemia that required aggressive intrauterine treatment.
A Japanese woman developed hydrops fetalis at the 29th week of gestation. Blood examination was highly positive for anti-Jr(a) antibodies. Cordocentesis demonstrated that the fetus had anti-Jr(a) antibodies and the lowest fetal hemoglobin concentration was 2.3 g/dl. After a total of four intravascular transfusions, fetal hydrops improved and a healthy girl of 2,120 g was delivered at the 35th week of gestation. The initial neonatal hemoglobin concentration at birth was 7.2 g/dl. After two straight transfusions, the infant's anemia did not worsen. Anti-Jr(a) antibodies became negative without developing hyperbilirubinemia.
The incidence of Jr(a) negativity can lead to underestimation of the risk of Jr(a) alloimmunization. This case shows that anti-Jr(a) alloimmunization may cause HDN and hydrops fetalis.
尽管新生儿Jr(a)溶血病(HDN)通常被认为病情较轻,但我们遇到了一例因极其严重的胎儿贫血导致的抗Jr(a)同种免疫性胎儿水肿,需要积极的宫内治疗。
一名日本女性在妊娠第29周时出现胎儿水肿。血液检查显示抗Jr(a)抗体呈强阳性。脐血穿刺显示胎儿存在抗Jr(a)抗体,胎儿血红蛋白最低浓度为2.3 g/dl。总共进行了4次血管内输血后,胎儿水肿得到改善,妊娠第35周时分娩出一名体重2120 g的健康女婴。出生时新生儿初始血红蛋白浓度为7.2 g/dl。连续两次输血后,婴儿贫血未加重。抗Jr(a)抗体转阴,未发生高胆红素血症。
Jr(a)阴性的发生率可能导致对Jr(a)同种免疫风险的低估。本病例表明,抗Jr(a)同种免疫可能导致HDN和胎儿水肿。