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[第一鳃裂畸形的管理与分类]

[Management and classification of first branchial cleft anomalies].

作者信息

Zhong Zhen, Zhao Enmin, Liu Yuhe, Liu Ping, Wang Quangui, Xiao Shuifang

机构信息

Department of Otolaryngology-Head and Neck Surgery, Peking University First Hospital, Beijing100034, China.

出版信息

Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 Jul;27(13):691-4.

Abstract

OBJECTIVE

We aimed to identify the different courses of first branchial cleft anomalies and to discuss the management and classification of these anomalies.

METHOD

Twenty-four patients with first branchial cleft anomalies were reviewed. The courses of first branchial cleft anomalies and their corresponding managements were analyzed. Each case was classified according to Olsen's criteria and Works criteria.

RESULT

According to Olsen's criteria, 3 types of first branchial cleft anomalies are identified: cysts (n = 4), sinuses (n = 13), and fistulas (n = 7). The internal opening was in the external auditory meatus in 16 cases. Two fistulas were parallel to the external auditory canal and the Eustachian tube, with the internal openings on the Eustachian tube. Fourteen cases had close relations to the parotid gland and dissection of the facial nerve had to be done in the operation. Temporary weakness of the mandibular branch of facial nerve occurred in 2 cases. Salivary fistula of the parotid gland occurred in one patient, which was managed by pressure dressing for two weeks. Canal stenosis occurred in one patient, who underwent canalplasty after three months. The presence of squamous epithelium was reported in all cases, adnexal skin structures in 6 cases, and cartilage in 14 cases. The specimens of the fistula which extended to the nasopharynx were reported as tracts lined with squamous epithelium (the external part) and ciliated columnar epithelium (the internal part). According to Work's criteria, 9 cases were classified as Type I lesions, 13 cases were classified as Type II lesions, and two special cases could not be classified. The average follow-up was 83 months (ranging from 12 to 152 months). No recurrence was found.

CONCLUSION

First branchial cleft anomalies have high variability in the courses. If a patient is suspected to have first branchial anomalies, the external auditory canal must be examined for the internal opening. CT should be done to understand the extension of the lesion. For cases without internal openings in the external auditory canal, CT fistulography should be done to demonstrate the courses, followed by corresponding treatment. Two special cases might be classified as a new type of lesions.

摘要

目的

我们旨在确定第一鳃裂畸形的不同病程,并讨论这些畸形的处理和分类。

方法

回顾了24例第一鳃裂畸形患者。分析了第一鳃裂畸形的病程及其相应的处理方法。每例病例均根据奥尔森标准和沃克斯标准进行分类。

结果

根据奥尔森标准,确定了3种类型的第一鳃裂畸形:囊肿(n = 4)、窦道(n = 13)和瘘管(n = 7)。16例的内口位于外耳道。2例瘘管与外耳道和咽鼓管平行,内口位于咽鼓管。14例与腮腺关系密切,手术中必须解剖面神经。2例出现面神经下颌支暂时麻痹。1例患者发生腮腺涎瘘,通过加压包扎两周进行处理。1例患者出现外耳道狭窄,3个月后接受外耳道成形术。所有病例均报告有鳞状上皮,6例有附属皮肤结构,14例有软骨。延伸至鼻咽部的瘘管标本报告为内衬鳞状上皮(外部)和纤毛柱状上皮(内部)的管道。根据沃克斯标准,9例被分类为I型病变,13例被分类为II型病变,2例特殊病例无法分类。平均随访83个月(范围为12至152个月)。未发现复发。

结论

第一鳃裂畸形的病程具有高度变异性。如果怀疑患者患有第一鳃裂畸形,必须检查外耳道是否有内口。应进行CT检查以了解病变的范围。对于外耳道无内口的病例,应进行CT瘘管造影以显示病程,然后进行相应的治疗。2例特殊病例可能被分类为一种新型病变。

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