So Hee Park, Hayeon Kim, Jeong In Choi, Soo-Ho Chung, Jae Hong Sang
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Thus, we diagnosed early HELLP syndrome and immediately started conservative treatments. One day after admission, symptoms and laboratory results showed aggravation of the disease. We performed termination, followed by dilation and curettage for retained placenta. Her general condition improved rapidly after the operation. Placen.tal biopsy showed both acute and chronic inflammation. She also had anticardiolipin antibody IgM, and after discharge, she was referred to a rheumatology specialist to address the antiphospho.lipid syndrome issue. Discussion: Although the triggers of HELLP syndrome are unclear, a recent inflammatory hypothesis suggests that placenta-derived inflammatory cytokines are involved. In our case, the anti-cardiolipin antibody may have triggered microangiopathy of the placenta. Our analysis of published HELLP cases revealed that, apart from the three diagnostic criteria, the most common abnormal laboratory finding was antiphospholipid antibodies. 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引用次数: 0
摘要
简介:溶血、肝酶升高和低血小板(HELLP)综合征是一种罕见的妊娠疾病,发生在妊娠20周前。我们报告一例HELLP综合征在妊娠14周和2天的发展。病例介绍:一名33岁的亚洲初产妇,妊娠14周零2天,以发烧和头痛就诊于急诊室。初始血压140/70 mm Hg,体温。体温38.5℃,心率130次/分,伴有心动过速。她的产前检查已经结束了。明显,胎儿超声检查在正常范围内。实验室结果显示血小板计数低,肝酶、d -二聚体和纤维蛋白原升高,但无黄疸迹象。她的白细胞鉴别提示是细菌感染。因此,我们早期诊断出HELLP综合征并立即开始保守治疗。入院后1天,症状及化验结果显示病情加重。我们进行了终止妊娠,随后对保留的胎盘进行了扩张和刮除。手术后她的一般情况迅速好转。Placen。活检显示急性和慢性炎症。她也有抗心磷脂抗体IgM,出院后,她被转介到风湿病专家解决抗磷问题。脂质综合征问题。讨论:尽管HELLP综合征的触发因素尚不清楚,但最近的一项炎症假说表明,胎盘源性炎症细胞因子参与其中。在我们的病例中,抗心磷脂抗体可能引发了胎盘微血管病变。我们对已发表的HELLP病例的分析显示,除了三个诊断标准外,最常见的实验室异常发现是抗磷脂抗体。因此,尽管罕见,如果患者出现炎症迹象,无论胎龄如何,考虑HELLP综合征是很重要的
HELLP Syndrome Developing at 14 Weeks of Gestation: An Extremely Rare Case Report and a Literature Review
Introduction: Hemolysis, elevated liver enzymes and low platelets (HELLP) syndrome is a disease of pregnancy that occurs very rarely before 20 weeks of gestation. We report a case of HELLP syndrome developing at 14 weeks and 2 days of gestation. Case Presentation: A 33-year-old Asian primipara at 14 weeks and 2 days of gestation visited the emergency room with a fever and headache. Initial blood pressure was 140/70 mm Hg, tempera.ture 38.5°C, heart rate 130 beats/min with tachycardia. Her prenatal examination has been unre.markable, and fetal ultrasonography was within normal range. The laboratory results showed low platelet count with elevated liver enzymes, D-dimer, and fibrinogen but no sign of jaundice. Her WBC differential suggested a bacterial infection. Thus, we diagnosed early HELLP syndrome and immediately started conservative treatments. One day after admission, symptoms and laboratory results showed aggravation of the disease. We performed termination, followed by dilation and curettage for retained placenta. Her general condition improved rapidly after the operation. Placen.tal biopsy showed both acute and chronic inflammation. She also had anticardiolipin antibody IgM, and after discharge, she was referred to a rheumatology specialist to address the antiphospho.lipid syndrome issue. Discussion: Although the triggers of HELLP syndrome are unclear, a recent inflammatory hypothesis suggests that placenta-derived inflammatory cytokines are involved. In our case, the anti-cardiolipin antibody may have triggered microangiopathy of the placenta. Our analysis of published HELLP cases revealed that, apart from the three diagnostic criteria, the most common abnormal laboratory finding was antiphospholipid antibodies. Therefore, despite its rarity, if a sign of inflammation is present in a patient, it is important to consider HELLP syndrome regardless of gestational age
期刊介绍:
Current Women"s Health Reviews publishes frontier reviews on all the latest advances on obstetrics and gynecology. The journal"s aim is to publish the highest quality review articles dedicated to research in the field. The journal is essential reading for all clinicians and researchers in the fields of obstetrics and gynecology.