Hseu Anne F, Spencer Grant P, Jo Stacy, Clark Roseanne, Nuss Roger C
Department of Otolaryngology and Communication Enhancement, Boston Children's Hospital, Boston, MA, USA; Department of Otolaryngology, Harvard Medical School, Boston, MA, USA.
Department of Otolaryngology and Communication Enhancement, Boston Children's Hospital, Boston, MA, USA.
Int J Pediatr Otorhinolaryngol. 2022 Jun;157:111118. doi: 10.1016/j.ijporl.2022.111118. Epub 2022 Mar 26.
Down syndrome is the most common chromosomal abnormality and is associated with a higher incidence of congenital heart defects, which often require surgery within the first year of life. Previous studies have found that children with Down syndrome are at higher risk for subglottic stenosis, vocal fold paralysis, and laryngomalacia. The goal of this study is to review children with Down syndrome presenting with dysphonia and to characterize their laryngeal pathologies.
A retrospective review was performed of patients with Down syndrome seen at a tertiary pediatric hospital's department of otolaryngology from Jan. 2007-Jul. 2021 for voice-related concerns. Inclusion criteria included age less than 18 years, diagnosis of Trisomy 21, and complaint of dysphonia. The data extracted included history of dysphonia, co-morbidities, demographic information, age at presentation, perceptual voice assessments, voice quality of life scores, acoustic data, laryngoscopic and/or videostroboscopic exams, and surgical procedures.
Twenty-three total patients met the study criteria. Of these children, 13 (57%) were male and 10 (43%) were female. The mean age at first presentation was 4.08 years (range 12 days-16.3 years). Eleven of the 23 patients presented within the first 12 months of life. Sixteen patients were diagnosed with vocal fold immobility, 13 of which were left-sided unilateral immobility and the remaining 3 were bilateral immobility. 5 patients were diagnosed with vocal fold nodules. 12 children in the immobility group had a history of cardiothoracic surgery at our institution. Only 3 patients had Consensus Auditory-Perceptual Evaluation of Voice (CAPE-V) assessments, though all three showed overall dysphonia ratings of severely deviant, with roughness and strain scores being the most severe.
The most common etiology of dysphonia in our Down syndrome patient population was vocal fold immobility and hypomobility, as opposed to vocal fold nodules (which is the most common in the general pediatric population). The higher likelihood of cardiac surgery in patients with Trisomy 21 may result in the increased incidence of vocal fold immobility. There should be a low threshold to refer dysphonic patients with Down syndrome for laryngoscopic evaluation, as treatment options may be available.
唐氏综合征是最常见的染色体异常疾病,与先天性心脏缺陷的较高发病率相关,这些心脏缺陷通常需要在生命的第一年内进行手术。先前的研究发现,唐氏综合征患儿发生声门下狭窄、声带麻痹和喉软化的风险更高。本研究的目的是回顾患有发声困难的唐氏综合征患儿,并描述他们的喉部病变特征。
对2007年1月至2021年7月在一家三级儿科医院耳鼻喉科就诊的唐氏综合征患者进行回顾性研究,这些患者存在与声音相关的问题。纳入标准包括年龄小于18岁、21三体综合征诊断以及发声困难主诉。提取的数据包括发声困难病史、合并症、人口统计学信息、就诊年龄、嗓音感知评估、嗓音生活质量评分、声学数据、喉镜和/或频闪喉镜检查以及手术操作。
共有23名患者符合研究标准。在这些儿童中,13名(57%)为男性,10名(43%)为女性。首次就诊的平均年龄为4.08岁(范围为12天至16.3岁)。23名患者中有11名在出生后的前12个月内就诊。16名患者被诊断为声带活动障碍,其中13名是左侧单侧活动障碍,其余3名是双侧活动障碍。5名患者被诊断为声带小结。活动障碍组中有12名儿童在我们机构有心胸外科手术史。只有3名患者进行了嗓音共识听觉-感知评估(CAPE-V),不过所有三名患者的总体发声困难评级均为严重异常,粗糙度和紧张度评分最为严重。
在我们的唐氏综合征患者群体中,发声困难最常见的病因是声带活动障碍和活动减弱,这与声带小结(这是一般儿科人群中最常见的病因)不同。21三体综合征患者进行心脏手术的可能性较高,这可能导致声带活动障碍的发病率增加。对于患有唐氏综合征且发声困难的患者,应降低进行喉镜评估的阈值,因为可能有治疗选择。