Aykut Serdar, Demir Suleyman Cansun, Evruke Ismaıl Cuneyt, Sucu Mete, Uzay Fatma Islek, Avan Mesut, Bayer Ozge Keles, Yalcin Emre
Department of Obstetrics and Gynecology Division of Maternal Fetal Medicine Cukurova University School of Medicine, Adana, Türkiye.
Case Rep Hematol. 2024 Jul 23;2024:1929147. doi: 10.1155/2024/1929147. eCollection 2024.
Hemolytic disease of the fetus and newborn (HDFN) is the development of anemia, hyperbilirubinemia, and finally hydrops fetalis in the fetus when antibodies to antigens on the surface of erythrocytes are transferred from the placenta to the fetus. The most common cause is D-HDFN. K (KEL1) from the Kell blood group system is the most potent immunogenic antigen after D among all blood group antigens. K-HDFN occurs in 0.1-0.3% of pregnant women. It accounts for 10% of cases of antibody-mediated severe fetal anemia. We present a successful management of Kell alloimmunization in a pregnant woman who had 3 times pregnancy loss with hydrops fetalis due to K-HDFN and who was proven to have K-HDFN in the postnatal period in her last pregnancy.
胎儿和新生儿溶血病(HDFN)是指当红细胞表面抗原的抗体经胎盘转移至胎儿时,胎儿发生贫血、高胆红素血症,最终发展为胎儿水肿。最常见的病因是D型HDFN。凯尔血型系统中的K(KEL1)是所有血型抗原中仅次于D的最具免疫原性的抗原。K型HDFN发生于0.1% - 0.3%的孕妇中。它占抗体介导的严重胎儿贫血病例的10%。我们报告了一例成功管理凯尔血型同种免疫的孕妇病例,该孕妇因K型HDFN曾有3次胎儿水肿流产史,且在其最后一次妊娠产后被证实患有K型HDFN。