...
首页> 外文期刊>European journal of pediatrics >What dose of intravenous immunoglobulin should be administered in Kawasaki disease with suspected systemic capillary leak syndrome?: Comment on: Shock: An unusual presentation of Kawasaki disease (Eur J Pediatr. 2011 Jul; 170(7):941-3)
【24h】

What dose of intravenous immunoglobulin should be administered in Kawasaki disease with suspected systemic capillary leak syndrome?: Comment on: Shock: An unusual presentation of Kawasaki disease (Eur J Pediatr. 2011 Jul; 170(7):941-3)

机译:患有系统性毛细血管渗漏综合症的川崎病,应给予何种剂量的静脉免疫球蛋白?:评论:休克:川崎病的一种不寻常表现(Eur J Pediatr。2011 Jul; 170(7):941-3)

获取原文
获取原文并翻译 | 示例
           

摘要

We read with great interest the contribution by Thabet et al. [6]. They reported an unusual case of Kawasaki disease (KD) presenting with hypotensive shock in a 5-month-old infant. Although intravenous immunoglobulins (IVIG) were initially infused with high suspicion of KD, giant coronary aneurysms occurred 16 days later, and the condition was considered as an IVIG-resistant form of KD. Reading the case report, however, we suspected a systemic capillary leak syndrome (SCLS) because of persistent hypoalbumi-nemia in this patient.The SCLS is a rare disease of reversible plasma extravasation and vascular collapse accompanied by hypo-albuminemia due to increased vascular leakage [1]. Patients with SCLS can experience shock and noncardiogenic edema that are treated with vasopressor therapy and colloid solutions for their osmotic effects.
机译:我们非常感兴趣地阅读了Thabet等人的论文。 [6]。他们报告了一个不寻常的川崎病(KD)病例,该患儿在一个5个月大的婴儿中出现了降压性休克。尽管最初高度怀疑KD的是静脉注射免疫球蛋白(IVIG),但16天后发生了巨大的冠状动脉瘤,该病被认为是KD的IVIG耐药形式。阅读该病例报告后,我们怀疑该患者由于持续性白蛋白血症持续存在系统性毛细血管渗漏综合征(SCLS).SCLS是一种罕见的可逆性血浆外渗和血管萎缩并伴有由于血管渗漏增加引起的低白蛋白血症的疾病[1]。患有SCLS的患者会经历休克和非心源性水肿,可采用血管加压药和胶体溶液治疗渗透压,以达到渗透作用。

著录项

相似文献

  • 外文文献
  • 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