Greenberg Max, Caloway Christen, Hersh Cheryl, Ryan Daniel, Goldenberg Paula, Hartnick Christopher
Rosalind Franklin University of Medicine and Science, Chicago Medical School, North Chicago, IL, USA; Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, MA, USA.
Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, MA, USA.
Int J Pediatr Otorhinolaryngol. 2019 May;120:130-133. doi: 10.1016/j.ijporl.2019.02.010. Epub 2019 Feb 13.
22q11.2 deletion syndrome is the most common microdeletion syndrome in children. Many patients with this disease develop craniofacial defects including cleft palate, bifid uvula, and velopharyngeal insufficiency. Our study adds to the current body of literature by describing a novel technique of carotid mobilization performed in conjunction with pharyngeal flap surgery in patients with extensive medialization of the carotid artery.
Carotid artery mobilization followed by insertion of a superiorly based pharyngeal flap was performed on two patients, a 10-year-old girl and a 5-year-old boy, with 22q11.2 deletion syndrome concurrent with velopharyngeal insufficiency.
Neither patient experienced significant post-operative issues. Following the procedure, parents of both patients noted significant speech and voice improvement. Both patients had improvements in VPI Effects On Life Outcome (VELO) scores, nasometry, and production of paragraph passages following surgery.
Our study describes a novel surgical treatment for children with 22q11.2 deletion syndrome with significant velopharyngeal insufficiency (VPI). The procedure wherein is characterized by an extensive mobilization of the carotid artery followed by implantation of a pharyngeal flap. This technique resulted in no significant intra-operative bleeding, and was measured to be successful as noted by nasometry scores and changes in pre- and post-op VELO scores.
22q11.2缺失综合征是儿童中最常见的微缺失综合征。许多患有这种疾病的患者会出现颅面缺陷,包括腭裂、悬雍垂裂和腭咽闭合不全。我们的研究通过描述一种在颈动脉广泛内移的患者中与咽瓣手术联合进行的颈动脉游离新技术,为当前的文献增添了内容。
对一名10岁女孩和一名5岁男孩这两名患有22q11.2缺失综合征并发腭咽闭合不全的患者进行了颈动脉游离,随后植入了蒂在上的咽瓣。
两名患者术后均未出现重大问题。手术后,两名患者的父母均指出其言语和嗓音有显著改善。两名患者术后的腭咽闭合不全对生活结果的影响(VELO)评分、鼻音测量以及段落朗读能力均有改善。
我们的研究描述了一种针对患有严重腭咽闭合不全(VPI)的22q11.2缺失综合征儿童的新型手术治疗方法。该手术的特点是对颈动脉进行广泛游离,随后植入咽瓣。该技术未导致术中大量出血,通过鼻音测量评分以及术前和术后VELO评分的变化表明手术取得了成功。