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Neonatal Alloimmune Thrombocytopenia Associated with Massive Chronic Intervillositis: A Case Report and Review of the Literature

机译:新生儿同种免疫性血小板减少症与大规模慢性间质炎相关:病例报告和文献复习。

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摘要

Neonatal alloimmune thrombocytopenia (NAIT) presents as isolated thrombocytopenia in a normal neonate as a result of destruction of fetal platelets by maternal antibodies against paternally derived human platelet antigens. Neonatal alloimmune thrombocytopenia affects 0.1% of births, with maternal antibodies crossing the placenta as early as 14 weeks' gestation. Few reports describe placental histopathological changes occurring in NAIT cases. We present a case of NAIT associated with massive chronic intervillositis, a rare entity occurring in 0.06% to 0.8% of reviewed 2nd- and 3rd-trimester placentas; to our knowledge, this is the 1st report of such an association.
机译:新生儿同种免疫血小板减少症(NAIT)在正常新生儿中表现为孤立的血小板减少症,这是由于抗父源性人类血小板抗原的母体抗体破坏了胎儿血小板的结果。新生儿同种免疫性血小板减少症影响0.1%的出生,母体抗体早在妊娠14周时就穿过胎盘。很少有报道描述在NAIT病例中发生的胎盘组织病理学变化。我们提出了一例与大面积慢性间质炎相关的NAIT,这是一种罕见的个体,发生在第二,三期妊娠胎盘的0.06%至0.8%之间;据我们所知,这是该协会的第一次报告。

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