...
首页> 外文期刊>Geburtshilfe und Frauenheilkunde >Chylomicronemia Syndrome in Pregnancy:a Case Report of an Acute Necrotizing Pancreatitis
【24h】

Chylomicronemia Syndrome in Pregnancy:a Case Report of an Acute Necrotizing Pancreatitis

机译:妊娠性糜烂血症综合征:急性坏死性胰腺炎1例报告

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Introduction; Chylomicronemia syndrome (CS) is a rare disorder characterized by a high level of tri-glycerides in plasma. We present a case of a pregnant woman with a severe acute pancreatitis (AP) affected by a CS.Case: A 38-year-old gravida 2, para 0 with an uneventful course of pregnancy was referred with an AP at 37 0/7 weeks of gestation. This diagnosis was made from a nearby hospital where the chemical analysis showed elevated pancreatic enzymes with significant hypertriglyceridemia. Because of a pathological fetal heart tracing a cae-sarean delivery was performed. The APGAR score of the female newborn was 5/8/8 at 1, 5 and 10 minutes, respectively. The pH from the umbilical cord were 7.26 (artery) and 7.59 (vein). Once transferred to our intensive care unit a computer tomography scan confirmed an onset of a necro-tizing AP. A conservative treatment was tried without success. For this reason a surgical de-bridement of the infected and necrosic parts was performed. After a long hospitalisation the patient could be dismissed after 2.5 months in good general condition.Discussion: Lipid profile changes in normal pregnancy are characterized by an elevation of total plasma cholesterol and triglyceride levels. This is normally caused by an increased liver synthesis of triglycerides in response to elevated estrogen levels. When a CS is diagnosed the main goal is to maintain fasting triglyceride levels at less than 500 mg/dL to reduce the risk for AP. Conclusion: Practitioners have an important role in evaluating chylomicronemic patients and implementing therapeutic lifestyle and pharmaceu-tic interventions aimed to reduce the risk for AP.
机译:介绍;糜烂性贫血综合征(CS)是一种罕见的疾病,其特征是血浆中甘油三酸酯水平高。我们介绍了一例患有CS的重症急性胰腺炎(AP)孕妇的案例。病例:一名38岁的妊娠2胎,妊娠过程平稳,第0段以37 0/7的AP进行了转诊怀孕几周。该诊断是从附近一家医院进行的,该医院的化学分析显示胰腺酶升高,伴有明显的高甘油三酯血症。由于病理性胎儿心脏追踪,进行了剖宫产术。在1、5和10分钟时,女性新生儿的APGAR得分分别为5/8/8。来自脐带的pH为7.26(动脉)和7.59(静脉)。一旦转移到我们的重症监护室,计算机断层扫描就会确认坏死性AP的发作。尝试了保守治疗没有成功。因此,对感染和坏死部位进行了外科清创术。长期住院后,患者可在一般情况良好的2.5个月后解散。这通常是由于雌激素水平升高引起的甘油三酸酯肝脏合成增加所致。诊断为CS后,主要目标是将空腹甘油三酯水平维持在500 mg / dL以下,以降低发生AP的风险。结论:从业者在评估乳糜微血症患者以及实施旨在降低AP风险的治疗性生活方式和药物干预措施中具有重要作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号