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先天性喉畸形的管理

Management of congenital laryngeal malformations.

作者信息

Sichel J Y, Dangoor E, Eliashar R, Halperin D

机构信息

Department of Otolaryngology/Head and Neck Surgery, Hadassah University Hospital, Jerusalem, Israel.

出版信息

Am J Otolaryngol. 2000 Jan-Feb;21(1):22-30. doi: 10.1016/s0196-0709(00)80120-9.

Abstract

Congenital malformations of the larynx are relatively rare but may be life-threatening. The most common causes include laryngomalacia, vocal cord paralysis, and subglottic stenosis. The last 20 years has seen major advances in the field of surgical correction of such anomalies also serving to reduce the number of tracheotomies in children and the inherent dangers they pose. Success rates for the most popular surgical procedures have been favorable. These include supraglottoplasty for cases of severe laryngomalacia, in which relief of respiratory symptoms has been shown to occur in excess of 80% of cases. Complication rate is low, although postoperative death has been reported. Failure usually occurs in patients with concomitant airway abnormalities including pharyngomalacia. Vocal cord lateralization for vocal cord paralysis with airway compromise is achieved by means of arytenoidopexy or arytenoidectomy, using the lateral approach. Arytenoidectomy also can be performed using laryngofissure or endoscopic laser excision. Subglottic stenosis is the 3rd most common congenital anomaly. Anterior or multiple cricoid splitting with cartilage graft interpositioning is usually performed. The success rates for these procedures has been shown to be approximately 90%.

摘要

先天性喉畸形相对少见,但可能危及生命。最常见的病因包括喉软化、声带麻痹和声门下狭窄。在过去20年里,此类畸形的外科矫正领域取得了重大进展,这也有助于减少儿童气管切开术的数量及其带来的固有风险。最常用手术的成功率令人满意。这些手术包括针对严重喉软化病例的声门上成形术,超过80%的此类病例术后呼吸症状得到缓解。并发症发生率较低,不过有术后死亡的报道。手术失败通常发生在伴有包括咽软化在内的气道异常的患者中。对于伴有气道受损的声带麻痹,通过采用外侧入路的杓状软骨固定术或杓状软骨切除术来实现声带外移。杓状软骨切除术也可通过喉裂开术或内镜激光切除术进行。声门下狭窄是第三常见的先天性畸形。通常采用前部或多处环状软骨裂开并植入软骨的手术方法。这些手术的成功率已显示约为90%。

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