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Idiopathic systemic capillary leak syndrome (SCLS): case report and systematic review of cases reported in the last 16 years.

机译:特发性系统性毛细血管渗漏综合征(SCLS):病例报告和最近16年来所报告病例的系统评价。

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摘要

'Idiopathic systemic capillary leak syndrome (SCLS), or Clarkson's disease is an unusual entity first described 45 years ago. It presents with recurrent episodes of shock due to leakage of the plasma, which is reflected by accompanying hemo-concentration, hypo-albuminemia and edema. We report the case of a young man with multiple episodes of shock with generalized edema and pleural effusion. An initial diagnosis of sepsis was made, but the lack of fever and absence of a demonstrable organism or source led to a revision of diagnosis to SLCS. The last review of this syndrome which analyzed 24 cases was published in 1990. Since then, 75 more cases have been reported. This article reviews these cases.
机译:特发性系统性毛细血管渗漏综合征(SCLS)或克拉克森氏病是45年前首次描述的不寻常实体。它表现为由于血浆渗漏而引起的休克复发发作,这可通过伴随的血药浓度,低白蛋白血症和水肿来反映。我们报道了一个年轻人多发性休克伴全身性水肿和胸腔积液的病例。最初诊断为败血症,但是由于没有发烧和缺乏可证实的生物体或来源,导致对SLCS的诊断有所改变。 1990年发表了对该综合征的最新综述,其中分析了24例病例。此后,又报告了75例病例。本文介绍了这些情况。

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