Narayanan Aravind, Date Rohit R, Birur Sanathkumar, Bhakta Pradipta, Srinivasan Sinnakirouchenane
Department of Anaesthesia & Intensive Care, Sultan Qaboos University Hospital, Muscat, Oman.
Sultan Qaboos Univ Med J. 2013 Aug;13(3):E467-71. doi: 10.12816/0003276. Epub 2013 Jun 25.
Hereditary angioedema (HAE) is a rare disorder caused by a deficiency of C1 esterase inhibitor. Minor trauma and emotional stress are the most common initiating events leading to contact system activation and excessive uncontrolled bradykinin release. This manifests as angioedema, a vascular reaction of the deeper layers of the skin and mucous membranes, with vasodilatation and increased permeability resulting in tissue swelling. Severe angioedema can occur in the perioperative period, leading to fatal airway obstruction. We describe the anaesthetic management of a child with HAE for dental rehabilitation and provide an review of the relevant literature.
遗传性血管性水肿(HAE)是一种由C1酯酶抑制剂缺乏引起的罕见疾病。轻微创伤和情绪应激是导致接触系统激活和缓激肽过度失控释放的最常见诱发因素。这表现为血管性水肿,即皮肤和黏膜深层的一种血管反应,伴有血管扩张和通透性增加,导致组织肿胀。严重的血管性水肿可发生在围手术期,导致致命的气道梗阻。我们描述了一名患有HAE的儿童进行牙齿修复的麻醉管理,并对相关文献进行了综述。