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第一鳃裂瘘管/窦道的临床表现、诊断与治疗:病例系列及文献综述

Clinical Manifestations, Diagnosis, and Management of First Branchial Cleft Fistula/Sinus: A Case Series and Literature Review.

作者信息

Liu Huan, Cheng Aoming, Ward Brent B, Wang Chong, Han Zhengxue, Feng Zhien

机构信息

Resident, Department of Oral and Maxillofacial-Head and Neck Oncology, Beijing Stomatological Hospital, Capital Medical University, Beijing, China.

Department Head, Division of Oral and Maxillofacial Surgery, Department of Surgery, University of Michigan, Ann Arbor, MI.

出版信息

J Oral Maxillofac Surg. 2020 May;78(5):749-761. doi: 10.1016/j.joms.2019.12.017. Epub 2020 Jan 7.

Abstract

PURPOSE

First branchial cleft fistula/sinus is a rare congenital developmental deformity that can sometimes be acquired from incision and drainage of a branchial cleft cyst. The aim of the present study was to explore the clinical manifestations, diagnosis, and surgical management of first branchial cleft fistula/sinus in both a large patient series and a review of the pertinent literature.

MATERIALS AND METHODS

The data from 31 cases diagnosed from February 2004 to April 2019 as first branchial cleft fistula/sinus were retrospectively reviewed. The patient demographic data and outcomes were explored. In addition, we performed a literature review of studies reported from 1923 to 2018 for first branchial cleft fistula/sinus and summarized those results.

RESULTS

The present study included 31 patients (15 males, 16 females) with a median age of 4 years. All the patients reviewed had presented with a unilateral first branchial cleft fistula/sinus. The parotid region was the most frequent site of presentation (41.9%) in these cases. The fistula/sinus had occurred on the left side in 13 patients (41.9%) and on the right side in 18 patients (58.1%). Of the 31 patients, 24 (77.4%) had acquired the disease from infection of an existing brachial cleft cyst or incomplete previous excision. Of the 31 cases, 28 (90%) had an intimate relationship between the tract and the facial nerve. Despite this close association, no patient developed postoperative facial nerve palsy. Of the 31 operations, 30 (97%) successfully accomplished complete resection with no recurrence postoperatively. Only 1 patient with a history of multiple recurrences experienced a subsequent recurrence, which was successfully treated with a second surgery.

CONCLUSIONS

First branchial cleft fistula/sinus is a frequently misdiagnosed and, therefore, undertreated entity, which leads to recurrence. It is closely associated with the facial nerve and extra auditory canal. The correct diagnosis and meticulous removal can be effectively achieved with minimal risk to the facial nerve.

摘要

目的

第一鳃裂瘘管/窦是一种罕见的先天性发育畸形,有时可由鳃裂囊肿切开引流引发。本研究旨在通过大量病例系列及相关文献回顾,探讨第一鳃裂瘘管/窦的临床表现、诊断及外科治疗方法。

材料与方法

回顾性分析2004年2月至2019年4月诊断为第一鳃裂瘘管/窦的31例患者的数据,探究患者人口统计学数据及治疗结果。此外,我们对1923年至2018年报道的第一鳃裂瘘管/窦的研究进行了文献回顾,并总结了相关结果。

结果

本研究纳入31例患者(男15例,女16例),中位年龄4岁。所有纳入研究的患者均表现为单侧第一鳃裂瘘管/窦。腮腺区是这些病例中最常见的发病部位(41.9%)。瘘管/窦发生在左侧13例(41.9%),右侧18例(58.1%)。31例患者中,24例(77.4%)因现有鳃裂囊肿感染或既往切除不完全而患病。31例病例中,28例(90%)的瘘管与面神经关系密切。尽管存在这种紧密关联,但无一例患者术后发生面神经麻痹。31例手术中,30例(97%)成功完成完全切除,术后无复发。仅1例有多次复发史的患者随后复发,二次手术成功治愈。

结论

第一鳃裂瘘管/窦是一种常被误诊且因此治疗不足的疾病,易导致复发。它与面神经和外耳道密切相关。正确诊断并细致切除可有效实现,同时将面神经损伤风险降至最低。

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