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首页> 外文期刊>Turkish Journal of Hematology >A case of Hydrops fetalis due to Kell alloimmunization: A perinatal approach to a rare case
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A case of Hydrops fetalis due to Kell alloimmunization: A perinatal approach to a rare case

机译:凯氏同种异体免疫接种致胎儿水肿一例:围产期罕见病例

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Introduction: While the routine administration of Rhesus immunoglobulin has significantly reduced the incidence of this type of alloimmunization, maternal alloimmunization to other red cell antigens continues to contribute to perinatal morbidity and mortality. Although the Kell antigen is found on the red cells of only 9% of the population, attention has increasingly been focused on Kell antibodies. Case Report: We present a case of fetal hydrops who was sonographically detected at 30th week of pregnancy. Antenatal tests for evaluation of fetal condition clearly showed the critical level of hemolytic disease but the baby was delivered prematurely due to fetal distress. The combination of anemia, reticulocytopenia, hydrops fetalis, and positive indirect Coombs test suggested Kell isoimmunization. The baby was treated by exchange transfusion with the Kell-negative packed red cell succesfully, and was discharged on postnatal 30th day. Conclusion: Here we describe a case of hydrops fetalis caused by Kell alloimmunization that was determined in postnatal period, and thus we plan to discuss the perinatal approach to the Kell immunization.
机译:简介:尽管常规给予恒河猴免疫球蛋白已大大降低了这种同种免疫的发生率,但母体对其他红细胞抗原的同种免疫仍继续导致围产期发病和死亡。尽管仅在9%的人口红细胞中发现了Kell抗原,但人们的注意力越来越集中在Kell抗体上。病例报告:我们提供一例胎儿水肿,在妊娠第30周通过超声检查发现。评估胎儿状况的产前检查清楚地表明了溶血性疾病的严重程度,但由于胎儿窘迫,婴儿早产了。贫血,网状细胞减少,胎儿积水和间接Coombs阳性试验的结合提示了Kell同种免疫。婴儿成功通过交换输注与凯尔阴性包装的红细胞进行治疗,并在出生后第30天出院。结论:在此我们描述了一例在出生后确定的由Kell同种免疫引起的胎儿水肿病例,因此我们计划讨论围产期Kell免疫的方法。

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