Suppr超能文献

灾难性抗磷脂综合征病理生理学的实验室研究

Laboratory studies on pathophysiology of the catastrophic antiphospholipid syndrome.

作者信息

Espinosa Gerard, Bucciarelli Silvia, Cervera Ricard, Gómez-Puerta José A, Font Josep

机构信息

Department of Autoimmune Diseases, Hospital Clínic, Barcelona, Catalonia, Spain.

出版信息

Autoimmun Rev. 2006 Dec;6(2):68-71. doi: 10.1016/j.autrev.2006.06.006. Epub 2006 Jul 18.

Abstract

The 'catastrophic' variant of the antiphospholipid syndrome (APS) is characterized by a diffuse thrombotic microvasculopathy. In contrast to the classical APS, single venous or arterial medium-to-large blood vessel occlusions are uncommon. The mechanisms of catastrophic APS are not clearly understood. In addition, there are no studies on pathophysiologic mechanisms of catastrophic APS. The clinical manifestations of catastrophic APS probably depend on (a) the organs affected by the thrombotic events and extent of the thrombosis and (b) manifestations of the systemic inflammatory response syndrome which are presumed to be due to excessive cytokine release from affected and necrotic tissues. The evident relationship between APS and infection may enable us to explain the development of catastrophic APS using the sepsis model. This is because catastrophic APS is characterized by multiple microvascular thrombotic events, of rapid onset, and causing multiorgan failure, a picture suggestive of septic shock, in which, there is a massive, acute inflammatory response.

摘要

抗磷脂综合征(APS)的“灾难性”变体以弥漫性血栓性微血管病为特征。与经典APS不同,单一静脉或动脉中到大血管闭塞并不常见。灾难性APS的机制尚不清楚。此外,目前尚无关于灾难性APS病理生理机制的研究。灾难性APS的临床表现可能取决于:(a)受血栓形成事件影响的器官以及血栓形成的程度;(b)全身炎症反应综合征的表现,推测这是由于受影响和坏死组织中细胞因子过度释放所致。APS与感染之间的明显关系或许能让我们利用脓毒症模型来解释灾难性APS的发展。这是因为灾难性APS的特征是多个微血管血栓形成事件,起病迅速,并导致多器官功能衰竭,这一情况提示为脓毒性休克,其中存在大规模的急性炎症反应。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验