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第一鳃裂畸形:39例病例研究及文献综述

First branchial cleft anomalies: a study of 39 cases and a review of the literature.

作者信息

Triglia J M, Nicollas R, Ducroz V, Koltai P J, Garabedian E N

机构信息

Department of Pediatric Otorhinolaryngology, La Timone Hospital, Marseille, France.

出版信息

Arch Otolaryngol Head Neck Surg. 1998 Mar;124(3):291-5. doi: 10.1001/archotol.124.3.291.

DOI:10.1001/archotol.124.3.291
PMID:9525513
Abstract

OBJECTIVES

To identify the clinical and anatomical presentations and to discuss the guidelines for surgical management of anomalies of the first branchial cleft.

DESIGN

Retrospective study.

SETTING

Three tertiary care centers.

PATIENTS

Thirty-nine patients with first branchial cleft anomalies operated on between 1980 and 1996.

INTERVENTION

All patients were treated surgically. Complete removal of the lesion required superficial parotidectomy with facial nerve dissection in 36 cases. The relationship of the facial nerve and anomalies is discussed.

RESULTS

Anatomically, 3 types of first branchial cleft anomalies are identified: fistulas (n=11), sinuses (n=20), and cysts (n=8). Clinically, 3 types of presentation are noted: chronic purulent drainage from the ear (n=12), periauricular swelling in the parotid area (n=18), and abscess or persistent fistula in the neck located above a horizontal plane passing through the hyoid bone (n=21). A membranous attachment between the floor of the external auditory canal and the tympanic membrane was observed in 10% of cases. The facial nerve was located lateral to the anomaly in 39% of cases.

CONCLUSIONS

Before definitive surgery, many patients (n=17) underwent incision and drainage for infection owing to the difficulties in diagnosing this anomaly. Wide exposure is necessary in most cases, and a standard parotidectomy incision allows adequate exposure of the anomaly and preservation of the facial nerve. Complete removal without complications depends on a good understanding of regional embryogenesis, a knowledge of the circumstances surrounding discovery, an awareness of the different anatomical presentations, and a readiness to identify and protect the facial nerve during resection.

摘要

目的

确定第一鳃裂畸形的临床和解剖学表现,并探讨其外科治疗指南。

设计

回顾性研究。

地点

三个三级医疗中心。

患者

1980年至1996年间接受手术治疗的39例第一鳃裂畸形患者。

干预措施

所有患者均接受手术治疗。36例患者需要行浅叶腮腺切除术并解剖面神经以彻底切除病变。讨论了面神经与畸形的关系。

结果

在解剖学上,确定了3种类型的第一鳃裂畸形:瘘管(n = 11)、窦道(n = 20)和囊肿(n = 8)。在临床上,注意到3种表现类型:耳部慢性脓性引流(n = 12)、腮腺区耳周肿胀(n = 18)以及位于穿过舌骨的水平面上方颈部的脓肿或持续性瘘管(n = 21)。10%的病例观察到外耳道底与鼓膜之间有膜性附着。39%的病例中面神经位于畸形外侧。

结论

由于诊断这种畸形存在困难,许多患者(n = 17)在确定性手术前因感染接受了切开引流。大多数情况下需要广泛暴露,标准的腮腺切除术切口可充分暴露畸形并保留面神经。无并发症的完整切除取决于对区域胚胎发育的良好理解、对发现情况的了解、对不同解剖学表现的认识以及在切除过程中识别和保护面神经的准备。

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