Sanuki Takuro, Watanabe Toshihiro, Kurata Shinji, Ayuse Takao
Associate Professor, Department of Clinical Physiology, Unit of Translational Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Staff anesthesiologist, Department of Dental Anesthesiology, Nagasaki University Hospital, Nagasaki, Japan.
J Oral Maxillofac Surg. 2014 Dec;72(12):2421.e1-3. doi: 10.1016/j.joms.2014.08.026. Epub 2014 Aug 27.
Hereditary angioedema (HAE) is a rare genetic disorder that causes a deficiency in or dysfunction of C1 esterase inhibitor (C1-INH) and is clinically characterized by sudden and recurrent attacks of angioedema. Although almost any part of the body can be affected, HAE is of greatest concern and can be life-threatening when the upper airway is involved, particularly the larynx (laryngeal attack). HAE attacks can be triggered by physical or psychological stress or can arise spontaneously without any apparent trigger. Dental treatments and routine oral surgical procedures, such as tooth extraction, abound with factors that can trigger an attack of HAE. Indeed, several cases of death resulting from HAE attacks have been reported after such procedures. Therefore, patients with HAE are of special concern in dentistry and require precautionary preparations before treatment. This report describes the successful management of tooth extractions in a patient with HAE who was at high risk of an HAE-induced laryngeal attack.
遗传性血管性水肿(HAE)是一种罕见的遗传性疾病,它会导致C1酯酶抑制剂(C1-INH)缺乏或功能障碍,临床特征为血管性水肿的突然发作和反复发作。尽管身体的几乎任何部位都可能受到影响,但当累及上呼吸道,尤其是喉部(喉发作)时,HAE最为令人担忧且可能危及生命。HAE发作可由身体或心理压力触发,也可能在没有任何明显诱因的情况下自发出现。牙科治疗和常规口腔外科手术,如拔牙,充满了可触发HAE发作的因素。事实上,已有数例此类手术后因HAE发作导致死亡的报道。因此,HAE患者在牙科领域备受关注,治疗前需要进行预防性准备。本报告描述了一名有HAE诱发喉发作高风险的HAE患者拔牙的成功管理。