Bilateral second branchial cleft fistulae coexisting with bilateral pre-auricular fistulae: A rare case report

IF 0.3 Q4 OTORHINOLARYNGOLOGY
H. Gong, Chunping Wu, Liang Zhou, L. Tao
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引用次数: 2

Abstract

Abstract Bilateral second branchial cleft fistulae are very rare and usually arise from the incomplete obliteration of the branchial apparatus during the embryonic period. Here, we present the clinical characteristics and surgical treatment of a case with bilateral second branchial cleft fistulae coexisting with bilateral pre-auricular fistulae. A 32-year-old man with complaints of a mucus-like discharge that was occasionally secreted on both sides of his neck at 2 years of age when swallowing or pressing the upper area of the two openings. He underwent surgical treatment. The fistulae tracts were traced ascending to the area adjacent to the internal and external carotid arteries, passing the glossopharyngeal and hypoglossal nerves, and opening into the tonsillar fossa finally. The correct diagnosis and definitive surgical excision should be made by a doctor who is familiar with the history, clinical examination, and anatomic structure of the different types of branchial anomalies.
双侧第二鳃裂瘘管并发双侧耳前瘘管1例
摘要双侧第二鳃裂瘘管非常罕见,通常是由于胚胎期鳃裂器官不完全闭塞引起的。本文报告一例双侧第二鳃裂瘘合并双侧耳前瘘的临床特点及手术治疗。32岁男性,主诉2岁时吞咽或按压两个开口上部时颈部两侧偶有粘液样分泌物。他接受了手术治疗。瘘束呈上升状至颈内外动脉附近,经过舌咽神经和舌下神经,最后进入扁桃体窝。正确的诊断和明确的手术切除应由熟悉不同类型支气管异常的病史、临床检查和解剖结构的医生做出。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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29 weeks
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