Mohd Nazri H, Noor Haslina M N, Shafini M Y, Noor Shaidatul Akmal A R, Rapiaah M, Wan Zaidah A
Universiti Sains Malaysia, School of Medical Sciences, Department of Hematology, 16150 Kubang Kerian, Kelantan.
Malays J Pathol. 2017 Apr;39(1):73-76.
Haemolytic disease of the foetus and newborn (HDFN) is caused by maternal red blood cells (RBC) alloimmunisation resulted from incompatibility of maternal and foetal RBCs. However, only a few HDFN attributed to anti-M were reported, varying from asymptomatic to severe anaemia with hydrops foetalis and even intrauterine death. A case of severe HDFN due to anti-M alloantibody from an alloimmunized grandmultiparous Malay woman with recurrent pregnancy loss is reported here. The newborn was delivered with severe and prolonged anaemia which required frequent RBC transfusions, intensive phototherapy and intravenous immunoglobulin administration. Although anti-M is rarely known to cause severe HDFN, a careful serological work-up and close assessment of foetal well-being is important, similar to the management of RhD HDFN. Alloimmunisation with anti-M type can lead to severe HDFN and even foetal loss.
胎儿及新生儿溶血病(HDFN)是由母婴红细胞(RBC)不相容导致母体红细胞同种免疫引起的。然而,仅有少数由抗-M引起的HDFN病例报道,症状从无症状到重度贫血伴胎儿水肿甚至宫内死亡不等。本文报道了一例来自一位多次妊娠失败的马来族经产妇的严重HDFN病例,该病例由抗-M同种抗体引起。新生儿出生时患有严重且持续的贫血,需要频繁输注红细胞、强化光疗及静脉注射免疫球蛋白。尽管抗-M很少引起严重的HDFN,但与RhD HDFN的处理类似,进行仔细的血清学检查及密切评估胎儿健康状况很重要。抗-M型同种免疫可导致严重的HDFN甚至胎儿丢失。