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妊娠中期严重特发性血小板减少症的成功管理。

Successful management of severe idiopathic thrombocytopenia in the second trimester of pregnancy.

作者信息

Antsaklis A, Papageorgiu I, Sindos M, Katsimanis E, Karaiskakis P, Michalas S

机构信息

Division of Maternal Fetal Medicine, First Department of Obstetrics and Gynecology, Alexandra Hospital, School of Medicine, University of Athens, Greece.

出版信息

Fetal Diagn Ther. 1998 Jul-Aug;13(4):233-5. doi: 10.1159/000020844.

Abstract

This paper describes a case of severe idiopathic thrombocytopenia in a primigravida. The disorder became symptomatic at 22 weeks gestation with a platelet count of 20,000/microliter. The existence of chronic idiopathic thrombocytopenia under remission was strongly suspected, but could not be documented. The patient was treated with oral corticosteroids over a period of 7 weeks. During this period, she also had three cycles of high-dose intravenous globulin. This treatment produced a transient improvement, but the platelet count fell to 4,000/ microl by the 29th gestational week. Caesarean section was carried out for maternal indication a week later, following a fourth intensified course of gamma-globulin, coupled with platelet transfusions and low-dose vinblastine. Splenectomy was not performed. Potentially life-threatening thrombocytopenia persisted for 6 weeks post partum. Despite the presence of circulating antiplatelet globulin in the maternal blood and the antenatal use of vinblastine, the infant was entirely unaffected and thrived.

摘要

本文描述了一例初产妇严重特发性血小板减少症的病例。该病症在妊娠22周时出现症状,血小板计数为20,000/微升。强烈怀疑存在处于缓解期的慢性特发性血小板减少症,但无法得到证实。患者接受了为期7周的口服皮质类固醇治疗。在此期间,她还进行了三个周期的大剂量静脉注射球蛋白治疗。这种治疗产生了短暂的改善,但到妊娠第29周时血小板计数降至4,000/微升。一周后,在进行了第四次强化的γ球蛋白疗程、输注血小板并使用小剂量长春碱后,因母亲的指征进行了剖宫产。未进行脾切除术。产后有潜在生命危险的血小板减少症持续了6周。尽管母体血液中存在循环抗血小板球蛋白且产前使用了长春碱,但婴儿完全未受影响且茁壮成长。

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