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一例罕见的妊娠相关性血栓性血小板减少性紫癜:诊断与管理中的挑战

A Rare Case of Pregnancy-Associated Thrombotic Thrombocytopenic Purpura: Challenges in Diagnosis and Management.

作者信息

Albousaeed Fatemah, AlmohammedAli Anwar, Alowainati Zainab, Salman Zainab, Alsubhi Mohammed

机构信息

College of Medicine and Health Sciences, Arabian Gulf University, Manama, BHR.

College of Medicine, Jordan University of Science and Technology, Irbid, JOR.

出版信息

Cureus. 2025 May 6;17(5):e83587. doi: 10.7759/cureus.83587. eCollection 2025 May.

Abstract

Thrombotic thrombocytopenic purpura (TTP) in pregnancy is a rare but potentially life-threatening condition that presents significant diagnostic challenges due to its overlapping features with other pregnancy-related disorders, such as preeclampsia and HELLP (hemolysis, elevated liver enzymes, and low platelet count) syndrome. We present the case of a 29-year-old gravida 2 para 1 woman at 35 weeks of gestation who presented with generalized weakness, nausea, and bruising, with laboratory findings indicating thrombocytopenia, microangiopathic hemolytic anemia, and schistocytes on peripheral blood smear. A diagnosis of pregnancy-associated TTP was made after excluding other causes such as preeclampsia. The patient was treated with plasma exchange, and her condition improved, leading to a successful cesarean section at 36 weeks of gestation. The neonatal outcome was favorable. This case highlights the importance of early recognition of TTP in pregnancy, as timely diagnosis and treatment with plasma exchange are critical for both maternal and fetal survival.

摘要

妊娠期血栓性血小板减少性紫癜(TTP)是一种罕见但可能危及生命的疾病,由于其与其他妊娠相关疾病(如子痫前期和HELLP(溶血、肝酶升高和血小板计数降低)综合征)有重叠特征,因此在诊断上面临重大挑战。我们报告一例29岁、孕2产1的女性,妊娠35周时出现全身乏力、恶心和瘀斑,实验室检查结果显示血小板减少、微血管病性溶血性贫血,外周血涂片可见裂红细胞。排除子痫前期等其他病因后,诊断为妊娠相关TTP。患者接受了血浆置换治疗,病情改善,于妊娠36周成功进行剖宫产。新生儿结局良好。该病例强调了妊娠期早期识别TTP的重要性,因为及时诊断并进行血浆置换治疗对母婴存活至关重要。

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