• 主题
高级搜索  >
历史搜索 清空历史
首页> 外文期刊>Gynecology, obstetrics & reproductive medicine : >Atypical HELLP Syndrome in a Pregnant Patient with Takayasu Arteritis and Subclavian to Axillary Artery Saphenous Vein Bypass Graft: A Case Report
【24h】

Atypical HELLP Syndrome in a Pregnant Patient with Takayasu Arteritis and Subclavian to Axillary Artery Saphenous Vein Bypass Graft: A Case Report

机译：孕妇高枝动脉炎并锁骨下至腋动脉大隐静脉旁路移植术的非典型HELLP综合征：一例报告

获取原文
           
页面导航
  • 摘要
  • 著录项
  • 相似文献
  • 相关主题

摘要

Takayasu arteritis (TA) is a rare chronic granulomatous inflammatory disease of the aorta and/or its?major branches, affecting mostly the vertebral, carotid, subclavian, iliac, and renal arteries. The disease?shows a striking predilection for women during the child-bearing years, and it is reasonable to expect at?least 1 pregnancy event in these women. Therefore, the management of pregnancies in patients with?this disease is of great importance to obstetricians. Here, we present the case of a patient with atypical?hemolysis, elevated liver enzymes, and low platelets (HELLP syndrome); this patient was receiving corticosteroid?therapy and had undergone subclavian-axillary artery saphenous vein graft for TA.
机译：Takayasu动脉炎（TA）是主动脉和/或其主要分支的一种罕见的慢性肉芽肿性炎性疾病，主要影响椎骨，颈动脉，锁骨下动脉，ilia动脉和肾动脉。这种疾病在育龄妇女中表现出惊人的喜好，因此可以预期这些妇女至少发生一次妊娠事件。因此，该病患者的妊娠管理对产科医生具有重要意义。在这里，我们介绍了一个非典型溶血，肝酶升高和低血小板（HELLP综合征）患者的病例。该患者正在接受皮质类固醇激素治疗，并已行锁骨下腋窝大隐静脉移植。

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