Jazbi B, Goodwin C, Tackett D, Faulkner S
Ann Otol Rhinol Laryngol. 1977 Sep-Oct;86(5 Pt 1):644-8. doi: 10.1177/000348947708600519.
A 2 1/2-year-old child was found to have subglottic stenosis with no obvious etiology. He initially responded well to dilatation, injection of triamcinolone and intermittent stenting of the airway, but four months later developed a marked, unyielding subglottic stenosis requiring tracheostomy. He had a gradual good response to dilatations and injections with triamcinolone and acquired a good subglottic lumen. However, he developed a recurrence following an episode of croup. Systemic steroids were added to the regimen leading to gradual resolution of the stenosis and successful decannulation. The embryogenesis of subglottic stenosis and the correlation with the known anatomy and histology are discussed. Subglottic stenosis may be congenital, traumatic, inflammatory, neoplastic or neurogenic. An additional group of patients has no obvious etiology and are classified as idiopathic. Treatment consists of various combinations of stents, systemic and intralesional steroids, dilatations and various operative procedures in the more refractory cases.
一名2岁半的儿童被发现患有声门下狭窄,病因不明。他最初对扩张、曲安奈德注射和气道间歇性支架置入反应良好,但四个月后出现严重的、顽固的声门下狭窄,需要进行气管切开术。他对扩张和曲安奈德注射逐渐产生良好反应,并获得了良好的声门下腔。然而,他在一次喉炎发作后复发。在治疗方案中加入全身用类固醇后,狭窄逐渐缓解,气管套管成功拔除。本文讨论了声门下狭窄的胚胎发生及其与已知解剖学和组织学的相关性。声门下狭窄可能是先天性、创伤性、炎性、肿瘤性或神经性的。另有一组患者病因不明,被归类为特发性。治疗包括支架、全身和病灶内类固醇、扩张以及在更难治的病例中采用各种手术程序的不同组合。