婴幼儿喉气管狭窄的外科治疗。

P Narcy, P Contencin, Y Menier, S Bobin, M Francois
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引用次数: 2

摘要

儿童喉气管狭窄是难以控制的,特别是在获得性病变的情况下。在317例病例中,我们报告了75例手术病例:28例是先天性的,47例是获得性的,主要是由于气管内插管。根据患者的年龄和状态、喉腔的大小、狭窄的确切位置和任何相关的异常情况,各种各样的喉气管成形术已被用于重建。Evans, Cotton和Rethi描述了使用的三种主要技术。支架植入依靠的是硅胶卷、蒙哥马利t型管和Aboulker特氟龙假体。65例患者的结果显示,先天性狭窄的通断率为92%,获得性狭窄的通断率为80%。为了减少治疗后的插管时间和产生语音障碍的后遗症,改进治疗似乎仍然是必要的。
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Surgical treatment of laryngotracheal stenosis in infants and children.

Laryngotracheal stenosis in children is difficult to manage, especially in cases of acquired lesions. Of 317 cases reviewed, 75 surgical cases are reported here: 28 were congenital and 47 acquired, mostly due to endotracheal intubation. A large variety of laryngotracheoplasty techniques have been used in reconstruction, depending on the age and status of the patient, the size of the laryngeal lumen, the exact site of the stenosis and any associated anomalies. The three main techniques used have been described by Evans, Cotton, and Rethi. Stenting relied on Silastic rolls, Montgomery T-tubes and Aboulker Teflon prostheses. The results in 65 patients showed a decannulation rate of 92% in cases of congenital stenosis and 80% in acquired ones. Improvements in therapy still seem necessary in order to reduce the cannulation time following treatment and the sequelae producing dysphonia.

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