Fraga J C, Schopf L, Forte V
Department of Pediatric Surgery, School of Medicine, and Graduate Program in Medicine, Surgery, Universidade Federal do Rio Grande do Sul, Rio Grande do Sul, Brazil.
J Pediatr Surg. 2001 Aug;36(8):1258-61. doi: 10.1053/jpsu.2001.25788.
BACKGROUND/PURPOSE: Laryngotracheoplasty has become an accepted treatment alternative for subglottic stenosis. However, the best autogenous material for laryngotracheoplasty remains controversial. Autogenous superior thyroid alar cartilage (TAC) has been used successfully in single stage laryngotracheal reconstruction in children with subglottic stenosis.
This is a retrospective study of 6 children (mean age, 16.6 months) undergoing TAC graft laryngotracheoplasty between September 1995, and June 1999. Two children had immediate tracheal intubation for congenital subglottic stenosis. Four others had previous tracheostomy: 3 for severe postintubation subglottic stenosis and 1 for congenital subglottic stenosis. After an anterior cricoid split, a piece of TAC was sutured between the cut ends of the cricoid, with the graft perichondrium facing intraluminally. Endotracheal intubation was maintained postoperatively.
Four children underwent successfully extubation 9 to 21 days (mean, 15.5 days) postoperatively. Two required tracheostomy, which was maintained because of severe laryngomalacia and laryngotracheobronchomalacia. One child was treated with CO2 laser because of symptomatic recurrence of the subglottic stenosis 3 weeks after the surgery; another required fundoplication for gastroesophageal reflux 12 months after laryngotracheoplasty. There were no donor site complications in any of the 6 cases. Repeat laryngoscopy and bronchoscopy showed a patent subglottic airway. All of them are without symptoms after a mean follow-up of 26 months.
(1) This preliminary experience indicates that the TAC graft technique is a viable option for laryngotracheal reconstruction; (2) the TAC graft has significant advantages, including a single operative incision and absence of donor-site morbidity.
背景/目的:喉气管成形术已成为声门下狭窄可接受的治疗选择。然而,用于喉气管成形术的最佳自体材料仍存在争议。自体甲状软骨上角(TAC)已成功用于声门下狭窄儿童的一期喉气管重建。
这是一项对1995年9月至1999年6月期间接受TAC移植喉气管成形术的6名儿童(平均年龄16.6个月)的回顾性研究。2名儿童因先天性声门下狭窄立即行气管插管。另外4名儿童曾行气管切开术:3名因严重插管后声门下狭窄,1名因先天性声门下狭窄。在环状软骨前部劈开后,将一块TAC缝合在环状软骨的断端之间,移植软骨膜面向管腔内。术后维持气管插管。
4名儿童术后9至21天(平均15.5天)成功拔管。2名儿童因严重喉软化和喉气管支气管软化而维持气管切开术。1名儿童在术后3周因声门下狭窄症状复发接受二氧化碳激光治疗;另1名儿童在喉气管成形术后12个月因胃食管反流需要行胃底折叠术。6例中无一例出现供区并发症。重复喉镜和支气管镜检查显示声门下气道通畅。平均随访26个月后,所有患儿均无症状。
(1)这一初步经验表明,TAC移植技术是喉气管重建的可行选择;(2)TAC移植具有显著优势,包括单一手术切口和无供区并发症。