Goudakos John K, Blioskas Sarantis, Psillas George, Vital Victor, Markou Konstantinos
1st Department of Otorhinolaryngology-Head and Neck Surgery, AHEPA University Hospital, Aristotle University of Thessaloniki, 54636 Thessaloniki, Greece.
Case Rep Otolaryngol. 2012;2012:924571. doi: 10.1155/2012/924571. Epub 2012 Nov 19.
The objective of the present paper is to describe the clinical presentation, diagnostic process, surgical treatment, and outcome of 2 patients with first branchial cleft anomaly. The first case was an 8-year-old girl presented with an elastic lesion located in the left infra-auricular area, in close relation with the lobule, duplicating the external auditory canal. The magnetic resonance imaging revealed a lesion, appearing as a rather well-circumscribed mass within the left parotid gland and duplicating the ear canal. A superficial parotidectomy was subsequently performed, with total excision of the cyst. The second patient was a 15-year-old girl presented with a congenital fistula of the right lateral neck. At superficial parotidectomy, a total excision of the fistula was performed. During the operation the tract was recorded to lay between the branches of the facial nerve, extending with a blind ending canal parallel to the external acoustic meatus. Conclusively, first branchial cleft anomalies are rare malformations with cervical, parotid, or auricular clinical manifestations. Diagnosis of first branchial cleft lesions is achieved mainly through careful physical examination. Complete surgical excision with wide exposure of the lesion is essential in order to achieve permanent cure and avoid recurrence.
本文的目的是描述2例第一鳃裂畸形患者的临床表现、诊断过程、手术治疗及结果。第一例是一名8岁女孩,其左耳下区域有一个弹性病变,与耳垂关系密切,外耳道呈双管状。磁共振成像显示一个病变,表现为左腮腺内边界相当清晰的肿块,外耳道呈双管状。随后进行了浅叶腮腺切除术,囊肿被完全切除。第二例患者是一名15岁女孩,右侧颈部有一个先天性瘘管。在浅叶腮腺切除术中,瘘管被完全切除。手术过程中发现瘘管位于面神经分支之间,以一个盲端管道平行于外耳道延伸。总之,第一鳃裂畸形是一种罕见的畸形,具有颈部、腮腺或耳部的临床表现。第一鳃裂病变的诊断主要通过仔细的体格检查来实现。为了实现永久治愈并避免复发,广泛暴露病变并进行完整的手术切除至关重要。