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[胎儿及新生儿同种免疫性血小板减少症]

[Fetal and neonatal alloimmune thrombocytopenias].

作者信息

Kaplan C

机构信息

Immunologie Plaquettaire, Institut National de la Transfusion Sanguine, 75739 Paris cedex 15, France.

出版信息

Transfus Clin Biol. 2009 May;16(2):214-7. doi: 10.1016/j.tracli.2009.03.013. Epub 2009 May 5.

Abstract

Fetal and neonatal alloimmune thrombocytopenias result from maternal immunization against fetal specific platelet antigens inherited from the father that the mother lacks. The incidence has been estimated to one in 800 to one in 1000 live births. The most feared complication in case of severe thrombocytopenia is the occurrence of intracranial hemorrhage, leading to death or neurological sequelea. The diagnosis is straightforward when a maternal alloantibody is detected and the offending antigen identified in the infant. Any difficulties in confirming the diagnosis should not delay the treatment. Since the first description of these conditions in the 1950's, significant progress has been made in laboratory diagnosis and management.

摘要

胎儿和新生儿同种免疫性血小板减少症是由于母亲针对从父亲遗传而来但母亲缺乏的胎儿特异性血小板抗原产生免疫反应所致。据估计,其发病率为每800至1000例活产中有1例。严重血小板减少症最可怕的并发症是颅内出血,可导致死亡或神经系统后遗症。当在母亲体内检测到同种抗体并在婴儿体内鉴定出致病抗原时,诊断很简单。确诊过程中遇到的任何困难都不应延误治疗。自20世纪50年代首次描述这些病症以来,实验室诊断和管理方面已取得了重大进展。

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