Isolated First Branchial Cleft Anomalies of the External Auditory Canal.

Alessandro Milani, Giuseppe Magliulo, Valeria Rossetti, Roberta Polimeni, Annalisa Pace
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Abstract

BACKGROUND Branchial cleft anomalies are congenital aberrations of the first to fourth pharyngeal pouches. First branchial cleft anomalies are classified into 2 subtypes according to anatomical and histological features. Their diagnosis can be difficult and depends on radiological and histological findings. In contrast, the required treatment is surgical removal, owing to the high risk of infection or malignancy. This case report introduces a first branchial cleft anomaly in an older woman with exclusive involvement of the external auditory canal (EAC). CASE REPORT This case report introduces a first branchial cleft anomaly in an 82-year-old woman with exclusive involvement of the EAC. She reported a history of mixed moderate hypoacusis and recurrent otitis media in the last year, without facial nerve involvement. Computed tomography and magnetic resonance imaging were performed to plan surgical treatment, which consisted of canaloplasty and Thiersch grafting. The histopathological examination on operative findings revealed a cystic lesion that was lined by cylindrical epithelium adjacent to the squamous cells, compatible with a diagnosis of first branchial arch malformative residues. CONCLUSIONS This is the unique case of first branchial cleft anomalies reported in an adult patient that exclusively involved the EAC. The onset of the disease was atypical, and surgery with the total removal of the lesion was the only possible treatment. Histopathology results revealed cylindric epithelium not represented in the EAC, compatible with first branchial arch malformative residues. This rare condition is a potential diagnostic option that should be considered in the differential diagnosis of cysts of the EAC.

Abstract Image

Abstract Image

孤立性第一鳃裂外耳道异常。
背景:鳃裂畸形是第一至第四咽袋的先天性畸形。根据解剖组织学特征,将鳃裂畸形分为2个亚型。他们的诊断可能是困难的,并取决于放射学和组织学结果。相反,由于感染或恶性肿瘤的高风险,所需的治疗是手术切除。这个病例报告介绍了一个老年妇女的第一鳃裂异常与外耳道(EAC)的独家累及。病例报告:本病例报告介绍了一例82岁女性的首次鳃裂异常,其完全累及EAC。她报告了去年混合性中度耳聋和复发性中耳炎的病史,没有面神经受累。进行计算机断层扫描和磁共振成像以计划手术治疗,包括管道成形术和Thiersch移植术。手术组织病理学检查显示一囊性病变,呈圆柱形上皮排列,与鳞状细胞相邻,符合第一鳃弓畸形残留的诊断。结论:这是一例单独涉及EAC的成人患者首次鳃裂异常。该疾病的发病不典型,手术切除病灶是唯一可能的治疗方法。组织病理学结果显示,EAC中未见圆筒状上皮,与第一鳃弓畸形残留物相符。这种罕见的情况是一个潜在的诊断选择,应考虑在鉴别诊断囊肿的EAC。
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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