Suppr超能文献

变形性斜头畸形伴悬雍垂畸形

Uvular malformation in the presence of deformational plagiocephaly.

作者信息

Archer Kaete, Marrinan Eileen, Stearns Susan, Tatum Sherard

机构信息

*Department of Otolaryngology and Communication Sciences †Department of Cell and Development Biology, State University of New York (SUNY) Upstate Medical University, Syracuse, NY.

出版信息

J Craniofac Surg. 2015 May;26(3):836-9. doi: 10.1097/SCS.0000000000001572.

Abstract

BACKGROUND

Deformational plagiocephaly is cranial asymmetry caused by external forces on the skull. Deformational plagiocephaly is seen in 5% to 48% of healthy newborns. Incomplete uvular fusion, in contrast, is one of many uvular malformations. The incidence of all degrees of incomplete uvular fusion is approximately 1% in healthy children. Bifid uvula is a malformation that is often considered a microform cleft palate or a marker for submucous cleft palate.

METHODS

This is a retrospective study of patients with deformational plagiocephaly seen at the Upstate Cleft and Craniofacial Center between January 1, 2006, and September 30, 2011. Patients were identified by the International Classification of Diseases, Ninth Revision code for plagiocephaly. Seventy-nine patients were excluded with craniosynostosis and syndromic diagnoses. One hundred forty-six patients with deformational plagiocephaly were included in the study. Data were collected for sex, age at presentation, parity, multiple births, delivery, oligohydramnios, cephalohematoma, uterine abnormalities, fetal position, and intrauterine growth restriction. Clinical findings were collected including location of cranial flattening and uvular malformations.

RESULTS

Twenty-four of 146 patients with deformational plagiocephaly had incomplete fusion of the uvula ranging from complete bifid uvula to a notched uvular tip (16.4%). This association was statistically significant (odds ratio, 18; 95% confidence interval, 11.1-28.9). Most patients (62.3%) were male. We recorded primiparity (44.5%), multiple births (17.1%), vacuum-assisted delivery (6.2%), cesarean section (36.3%), oligohydramnios (4.1%), uterine abnormalities (2.1%), abnormal fetal position (3.4%), and intrauterine growth restriction (1.4%). Ten of the 24 patients with plagiocephaly and uvular malformation were seen for an initial consultation only in our chart system. Of the remaining 14 patients with follow-up, none had recorded signs or symptoms of velopharyngeal insufficiency.

CONCLUSIONS

The incidence of incomplete uvular fusion in infants with deformational plagiocephaly is 16.4%, which is significantly higher than the approximate 1% incidence reported in the general population. This is the first report of uvular malformation in the presence of deformational plagiocephaly.

摘要

背景

变形性斜头畸形是由颅骨上的外力导致的颅骨不对称。在5%至48%的健康新生儿中可见变形性斜头畸形。相比之下,悬雍垂融合不全是众多悬雍垂畸形之一。在健康儿童中,各种程度的悬雍垂融合不全的发生率约为1%。双裂悬雍垂是一种常被认为是微小型腭裂或黏膜下腭裂标志的畸形。

方法

这是一项对2006年1月1日至2011年9月30日在北部腭裂与颅面中心就诊的变形性斜头畸形患者的回顾性研究。通过国际疾病分类第九版中斜头畸形的编码来识别患者。79例患有颅缝早闭和综合征诊断的患者被排除。146例变形性斜头畸形患者被纳入研究。收集了性别、就诊年龄、产次、多胎妊娠、分娩方式、羊水过少、头颅血肿、子宫异常、胎儿位置和宫内生长受限等数据。收集了临床发现,包括颅骨扁平的位置和悬雍垂畸形。

结果

146例变形性斜头畸形患者中有24例存在悬雍垂融合不全,范围从完全双裂悬雍垂到悬雍垂尖端有缺口(16.4%)。这种关联具有统计学意义(优势比为18;95%置信区间为11.1 - 28.9)。大多数患者(62.3%)为男性。我们记录了初产(44.5%)、多胎妊娠(17.1%)、真空辅助分娩(6.2%)、剖宫产(36.3%)、羊水过少(4.1%)、子宫异常(2.1%)、异常胎儿位置(3.4%)和宫内生长受限(1.4%)。24例患有斜头畸形和悬雍垂畸形的患者中有10例仅在我们的病历系统中进行了初次咨询。在其余14例有随访的患者中,没有记录到腭咽闭合不全的体征或症状。

结论

变形性斜头畸形婴儿中悬雍垂融合不全的发生率为16.4%,显著高于一般人群中报道的约1%的发生率。这是关于变形性斜头畸形存在时悬雍垂畸形的首次报告。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验