Lipitz S, Ryan G, Murphy M F, Robson S C, Haeusler M C, Metcalfe P, Kelsey H, Rodeck C H
Fetal Medicine Unit, University College Hospital, London, U.K.
Prenat Diagn. 1992 Nov;12(11):955-8. doi: 10.1002/pd.1970121116.
Neonatal alloimmune thrombocytopenia (NAIT), which usually involves sensitization to P1A1 (HPA-1a), may have devastating complications for the fetus. These may be prevented by antenatal treatment of severe cases with either maternally administered high-dose gamma-globulin and/or repeated intrauterine platelet transfusions. Determination of the paternal platelet phenotype is useful for counseling parents who have had one or more affected pregnancies. This report of an unaffected pregnancy in a woman with a history of previous pregnancies complicated by NAIT illustrates the role of paternal and fetal platelet phenotyping in managing existing pregnancies at risk of NAIT.
新生儿同种免疫性血小板减少症(NAIT)通常涉及对P1A1(HPA-1a)的致敏,可能会给胎儿带来毁灭性的并发症。对于严重病例,可通过母亲给予高剂量γ球蛋白和/或反复进行宫内血小板输注进行产前治疗来预防这些并发症。确定父亲的血小板表型有助于为有过一次或多次受影响妊娠的父母提供咨询。本报告介绍了一名有NAIT既往妊娠史的女性此次未受影响的妊娠情况,阐明了父亲和胎儿血小板表型分析在管理有NAIT风险的现有妊娠中的作用。