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小儿单侧孤立性后鼻孔闭锁与下颌骨髁突发育不良无关。

Pediatric unilateral isolated choanal atresia is not associated with mandibular condyle hypoplasia.

机构信息

Department of Otolaryngology-Head and Neck Surgery, Emory University School of Medicine, Atlanta, GA, United States of America.

Department of Radiology and Imaging Sciences, Emory University School of Medicine, Atlanta, GA, United States of America; Department of Radiology, Children's Healthcare of Atlanta, Atlanta, GA, United States of America.

出版信息

Am J Otolaryngol. 2021 Jan-Feb;42(1):102824. doi: 10.1016/j.amjoto.2020.102824. Epub 2020 Nov 12.

Abstract

PURPOSE

We hypothesized that the ontogeny of unilateral isolated choanal atresia involves a field defect manifesting as ipsilateral mandibular condylar hypoplasia. The topic is important because the mechanism of the unilateral isolated choanal atresia is unknown.

MATERIALS AND METHODS

Retrospective self-controlled case series. We included 20 patients (2 males and 18 females, ages 2 weeks to 13 years) with unilateral isolated non-syndromic choanal atresia. We studied their high-resolution computed tomographic scans. Two otolaryngologists measured the largest cross-sectional area of the mandibular condyle in the axial plane perpendicular to the posterior border of each mandibular ramus independently. Statistical significance and inter-rater agreement were calculated with paired Wilcoxon rank sum test and Spearman's non-parametric correlation coefficient respectively.

RESULTS

Cross-sectional areas of the condyles ipsilateral to the choanal atresia were not statistically different than those of the contralateral condyle (P = 0.27). Inter-observer agreement of condyle areas was excellent: Spearman's r = 0.85 on the right and r = 0.94 on the left.

CONCLUSIONS

In this cohort of children with the rarity of isolated non-syndromic unilateral congenital choanal atresia, no associated mandibular condyle hypoplasia was found. The data suggest that the underlying ontogeny was unlikely attributable to a field defect.

摘要

目的

我们假设单侧孤立性后鼻孔闭锁的发生机制与同侧下颌骨髁突发育不良的局灶性缺陷有关。本研究的主题非常重要,因为单侧孤立性后鼻孔闭锁的发生机制尚不清楚。

材料和方法

这是一项回顾性自身对照病例系列研究。我们纳入了 20 名单侧孤立性非综合征性后鼻孔闭锁患者(2 名男性和 18 名女性,年龄 2 周至 13 岁),研究了他们的高分辨率计算机断层扫描。两位耳鼻喉科医生分别在垂直于下颌支后缘的轴位平面上测量了每侧下颌骨髁突的最大横截面积。使用配对 Wilcoxon 秩和检验和 Spearman 非参数相关系数分别计算统计显著性和观察者间一致性。

结果

患侧与健侧的髁突横截面积无统计学差异(P=0.27)。髁突面积的观察者间一致性极好:右侧 r=0.85,左侧 r=0.94。

结论

在本队列中,单侧孤立性非综合征性先天性后鼻孔闭锁患儿罕见,并未发现同侧下颌骨髁突发育不良。这些数据表明,其潜在的发生机制不太可能归因于局灶性缺陷。

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