期刊文献+

2747例感音神经性聋内耳畸形分类的研究 被引量:12

Study on 2 747 cases of inner ear malformation for its classification in patient with sensorineural hearingloss
原文传递
导出
摘要 目的:研究大宗病例高分辨率CT资料,了解中国人感音神经性聋患者群体内耳畸形的发病情况,探讨内耳畸形分类的依据。方法:对2 747例感音神经性聋患者的资料进行回顾性分析,按照Sennaroglu分类方法对患者的内耳CT检查结果进行分类研究。结果:1发现内耳畸形843例(30.69%);2843例内耳畸形中耳蜗畸形占52.31%(441/843),单纯前庭导水管畸形占40.33%(340/843),单纯前庭/半规管/内耳道畸形占7.35%(62/843);3441例耳蜗畸形中Michel畸形占1.13%(5/441),耳蜗未发育占1.81%(8/441),共同腔畸形占3.17%(14/441),IP-Ⅰ畸形占8.62%(38/441),耳蜗发育不全占9.07%(40/441),Mondini畸形(伴大前庭水管)占76.19%(336/441)。结论:通过高分辨率CT检查发现中国人感音神经性聋患者群体中存在较高的内耳畸形发病率,Sennaroglu分类方法对于各类内耳畸形发病率的流行病学统计具有重要的指导意义。 Objective:Analyze the data of the patients with sensorineural hearing loss in China and study the classification and incidence of inner ear malformationsby the high-resolution computed, tomography. Method: The investigation took a retrospective review of CT findings relating to the 2 747 cases of outpatients. The inner ear malformations diagnosed by CT were classified according to the methods proposed by Sennaroglu. Result:(1)843 cases of inner ear malformations were found in 2 747 cases of patients with sensorineural hearing loss by CT examination. The incidence of inner ear malformation was 30.69 % (843/2 747). (2)The epidemiological information of 843 cases of inner ear malformation according to Sennaroglu's classification was as follows: cochlea was 52.31 % (441/ 843), simple vestibular aqueduct was 40.33% (340/843), simple vestibular/ semicircular canal/ internal auditory canal were 7.35%(62/843) of the group. (3)441 cases of cochlea malformation were consisted of these types of malformation: Michel deformity was 1.13%(5/441), cochlear aplasia was 1.81%(8/441), common cavity deformity was 3.17%(14/441), incomplete partition type I was 8.62%(38/441), cochlea hypoplasia was 9.07% (40/441) and incomplete partition type Ⅱ was 76. 19%(336/441) of the group. Conclusion:The results suggested that 30.69% cases of inner ear malformation can be found in patients with sensorineural hearing loss, which is more higher than reported by the high-resolution computed tomography. Sennaroglu's classification is instructively significant in investigating the status of inner ear malformations.
出处 《临床耳鼻咽喉头颈外科杂志》 CAS 北大核心 2015年第1期45-47,共3页 Journal of Clinical Otorhinolaryngology Head And Neck Surgery
基金 国家自然科学基金重点项目(No:81230020) 国家自然科学基金面上项目(No:81371096 No:30371610)
关键词 感音神经性 内耳畸形 hearing loss sensorineural inner ear malformation
  • 相关文献

参考文献10

  • 1CROSS N C,STEPHENS S D G,FRANCIS M,et al.Computed tomography evaluation of the inner ear as a diagnostic,counseling and management strategy in patients with congenital sensorineural hearing impairment[J].Clin Otolaryngol,1999,24:235-238.
  • 2SENNAROGLU L,SAATCI I.A new classification for cochleovestibular malformations[J].Laryngoscope,2002,112:2230-2241.
  • 3李幼瑾,杨军,李蕴.感音神经性聋患儿中先天性内耳畸形的构成、影像学及临床听力学特征[J].临床耳鼻咽喉头颈外科杂志,2011,25(1):1-5. 被引量:28
  • 4程岚,吴皓,杨军,陶峥,李蕴,侯峥,李玉华.儿童先天性感音神经性聋中内耳畸形的影像学分析[J].上海交通大学学报(医学版),2007,27(1):29-32. 被引量:7
  • 5SCHUKNECHT H F.Pathology of the ear[M].2nd ed.Philadelphia:Lea and Febiger,1993:180-181.
  • 6SHIM H J,SHIN J E,CHUNG J W,et al.Inner ear anomalies in cochlear implantees:importance of radiologic measurements in the classification[J].Otol Neurotol,2006,27:831-837.
  • 7KABATOVA Z,PROFANT M,SIMKOVA L,et al.Cochlear implantation in malformed inner ear[J].Bratisl Lek Listy,2009,110:609-613.
  • 8杨军,樊碧云,李幼瑾,吴皓.关于内听道、耳蜗神经管及耳蜗神经畸形分型的建议[J].临床耳鼻咽喉头颈外科杂志,2014,28(16):1185-1187. 被引量:14
  • 9LOW W M.Imaging of cochlear and auditory brain stem implantation[J].Am J Neuroradiol,1998:1147-1154.
  • 10SLATTERY W H,LUXFORD W M.Cochlear implantation in the congenital malformed cochlea[J].Laryngoscope,1995,105:1184-1187.

二级参考文献27

  • 1包颜明,赵光明,宋光义.内耳高分辨率CT的应用[J].放射学实践,2004,19(7):526-528. 被引量:10
  • 2杨军.对先天性内耳畸形的再认识[J].临床耳鼻咽喉科杂志,2006,20(22):1049-1051. 被引量:11
  • 3JOHNSON J, LALWANI A K. Sensorineural and conductive hearing loss associated with lateral semicircular canal malformation[J]. Laryngoscope, 2000, 110:1673--1679.
  • 4FERREIR T, SHAYESTEHFAR B, LUFKIN R. Narrow,duplicated internal auditory canal[J]. Neuroradiology, 2003,45 : 308 -- 310.
  • 5CHRISTINE M, DAVIDSON H C, HARNSBERG ER H R, et al. Imaging findings of cochlear nerve de ficiency[J]. AJNR Am J Neuroradiol, 2002,4 : 635-643.
  • 6JOHN E, TANDY R, GRUNDFAST K, et al. Ma jor and minor temporal bone abnormalities in children with and without congenital sensorineural hearing loss [J]. Arch Otolaryngol Head Neck Surg, 2002,128: 664--671.
  • 7PINTO J A, MELLO C F Jr, MARGUI A C, et al. Enlarged vestibular aqueduct syndrome: report of 3 cases and literature review[J]. Braz J Otorhinolaryngol, 2005,71:386--391.
  • 8OKAMOTO K, ITO J, FURUSAWA T, et al. MRI of enlarged endolymphatic sacs in the large vestibular aqueduct syndrome [J], Neuroradiology, 1998, 40: 167- 172.
  • 9JOSEPH A, GRIMMER J F, HEDLUND G, et al. Cohlear abnormalities associated with enlarged vestibular aqueduct anomaly[J]. Int J Pediatr Otorhinolar yngol, 2009,73:1682--1685.
  • 10SENNAROGLU L, SATTIC I. A new classification for cochleovestibula malformations [J]. Laryngoscope, 2002,112:2230--2241.

共引文献44

同被引文献89

引证文献12

二级引证文献33

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部