Ueha Rumi, Goto Takao, Kaneoka Asako, Takano Tomonori, Sato Taku, Hirata Yoichiro, Nito Takaharu, Yamasoba Tatsuya
Department of Otolaryngology, The University of Tokyo, Tokyo, Japan.
Department of Otolaryngology, The University of Tokyo, Tokyo, Japan.
Auris Nasus Larynx. 2018 Oct;45(5):1121-1126. doi: 10.1016/j.anl.2018.03.010. Epub 2018 Apr 16.
Laryngeal clefts are rare congenital malformations of the posterior part of the larynx. The severities are correlated with the downward extension of the cleft and can involve numerous clinical symptoms including dysphagia and respiratory distress. As significant comorbidities may be present, individual treatments depend on the child's general condition and type of cleft involved. Herein, we describe two cases of children with laryngeal clefts and severe comorbidities requiring mechanical ventilation. One child with type III laryngeal cleft was successfully managed with the lateral pharyngotomy approach. The other child with type II laryngeal cleft has not been able to undergo cleft-closure surgery because of severe general conditions, therefore has continued training for feeding and swallowing.
喉裂是喉部后部罕见的先天性畸形。其严重程度与裂孔向下延伸有关,可涉及多种临床症状,包括吞咽困难和呼吸窘迫。由于可能存在重大合并症,个体化治疗取决于患儿的一般状况和所涉及的裂孔类型。在此,我们描述两例患有喉裂且伴有严重合并症需要机械通气的儿童病例。一名患有III型喉裂的儿童通过侧咽切开术成功治疗。另一名患有II型喉裂的儿童由于一般状况严重,未能接受裂孔闭合手术,因此继续进行喂养和吞咽训练。