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[腭裂合并中耳胆脂瘤患儿的临床特征]

[Clinical characteristics in children with cleft palate associated with middle ear cholesteatoma].

作者信息

Yang Y, Chen M, Hao J S, Liu W, Zhang J

机构信息

Department of Otorhinolaryngology Head and Neck Surgery, Beijing Children's Hospital, Capital Medical University, Beijing 100045, China.

出版信息

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2017 May 7;52(5):377-380. doi: 10.3760/cma.j.issn.1673-0860.2017.05.011.

Abstract

To summarize the characteristics of children diagnosed as cleft palate associated with middle ear cholesteatoma. There were five middle ear cholesteatoma cases who had previously received cleft palate repairment surgery. All of the patients were followed up for 17 to 47 months. Median follow-up time was 31 months. There were three males and two females with three to eleven years old , and the average of age was seven years and ten months. The time of cleft palate repairment surgery was from six months to four years, and the average age was one year and nine months. No history of grommet insertion. Three cases were unilateral choleateatoma (right ear in two cases and left ear in one case, of which two cases of contralateral ear with secretory otitis media) and two cases were bilateral choleateatoma. Five cases(seven ears) received surgeries. Radical mastoidectomy + canal wall down tympanoplasty were performed in three ears, in which we found stapes disappeared. Radical mastoidectomy + canal wall up tympanoplasty were performed in four ears, in which we found intact foot plate, with recurrence occurred in one case nine months after the first surgery. No recurrence occurred after the second canal wall down tympanoplasty. The postoperative average hearing thresholds of air conduction were improved in different degrees. There may be a relationship between cleft palate associated with middle ear cholesteatoma and no grommet insertion history. The incidence of bilateral cases is relatively high, and otitis media with effusion may occur because of poor Eustachian tube function in the unilateral cases. Choice of surgical methods should be decided basing on combination of decreasing the recrudescence and improving the hearing.

摘要

总结诊断为腭裂伴中耳胆脂瘤患儿的特征。有5例中耳胆脂瘤患者曾接受腭裂修复手术。所有患者均随访17至47个月,中位随访时间为31个月。有3名男性和2名女性,年龄3至11岁,平均年龄为7岁10个月。腭裂修复手术时间为6个月至4岁,平均年龄为1岁9个月。无鼓膜置管史。3例为单侧胆脂瘤(2例右耳,1例左耳,其中2例对侧耳伴分泌性中耳炎),2例为双侧胆脂瘤。5例(7耳)接受了手术。3耳行根治性乳突切除术+开放式鼓室成形术,其中发现镫骨消失。4耳行根治性乳突切除术+完壁式鼓室成形术,其中发现足板完整,1例在首次手术后9个月复发。二次开放式鼓室成形术后无复发。术后气导平均听阈均有不同程度改善。腭裂伴中耳胆脂瘤可能与无鼓膜置管史有关。双侧病例发生率相对较高,单侧病例可能因咽鼓管功能不良而发生中耳积液。手术方法的选择应基于降低复发率和提高听力的综合考虑来决定。

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