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先天性喉蹼为少见的先天性畸形。笔者于1987～1989年在非洲乌干达金贾市医院工作期间曾诊治1例。患儿,男,13岁。黑种人。出生后即严重声嘶、音低、哮喘,若遇感冒、发热或剧烈活动时则呼吸困难加重。直接喉镜检查:声门前2/3为表面光滑的淡红色蹼,蹼较厚,与两侧声带相连,声门后1/3为圆形小孔、直径约3mm。因患儿呼吸困难,在全麻下先行气管切开术,从气管切开开口放入麻醉插管,插管时发现气管较正常儿童明显狭窄;继而行喉
Congenital laryngeal web for rare congenital malformations. The author in 1987 ~ 1989 in Uganda, Jinja City Hospital worked during the diagnosis and treatment of 1 case. Children, male, 13 years old. black people. Serious hoarseness after birth, low tone, asthma, in case of a cold, fever or severe activity, then increased dyspnea. Direct laryngoscopy: glottis 2/3 for the smooth surface of the light-red webbed, web thicker, connected with the vocal cords on both sides of the glottis after 1/3 is a circular hole diameter of about 3mm. Due to children with dyspnea, the first tracheotomy under general anesthesia, anesthesia intubation from the tracheotomy opening into the trachea, tracheal intubation was significantly narrower than normal children; followed by throat