MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1097/mao.0000000000004691

Медицинская библиотека · Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology · 2025

Clinical Characteristics of a Rare Type I Congenital First Branchial Cleft Anomaly With Native Sinus Tract.

Luo Wenwei, Mao Weilong, Sheng Xiaoli, Xu Xianzhen, Xu Mimi, Chen Liangsi

СтатьяПеревод в очереди

Аннотация

OBJECTIVES

We present an unusual type I congenital first branchial cleft anomaly (CFBCA) characterized by a distinct sinus tract in the superior wall of the cartilaginous external auditory canal (EAC), classified as the sinus variant of type I congenital first branchial cleft anomalies (CFBCAs). This study aims to characterize its distinctive clinical features and present management approaches for this rare entity.

METHODS

Medical records of patients undergoing excision for sinus variant of type I CFBCAs between January 2007 and September 2023 (a 16-y period) were retrospectively analyzed. Clinical characteristics, therapeutic interventions, histopathologic diagnoses, and long-term outcomes were systematically catalogued.

RESULTS

The sinus variant of type I CFBCAs is a rare manifestation of CFBCAs, accounting for 11 of 188 cases (5.9%) in our series. Cardinal clinical features included recurrent periauricular inflammation (9/11 cases, 81.8%), with all cases demonstrating a characteristic concealed sinus orifice at the superior cartilaginous EAC (11/11 cases, 100%). All patients (11/11 cases, 100%) were initially misdiagnosed as lymphadenitis, epidermal cysts, or localized infections. The concealed sinus orifices at the superior cartilaginous EAC were frequently overlooked, with definitive diagnosis established by visual inspection in only 3 patients (3/11 cases, 27.3%). In the remaining 8 patients (8/11 cases, 72.7%), occult sinus orifices were identified through combined palpation and visual inspection. All lesions originated exclusively from the superior cartilaginous EAC (11/11 cases, 100%) and maintained a relative simple relationship with the facial nerve trunk (11/11 cases, 100%). Complete surgical excision of the sinus tract along with any adherent periauricular cysts was determined to be the optimal treatment approach.

CONCLUSIONS

Clinicians should maintain a high index of suspicion for the sinus variant of type I CFBCAs when evaluating pediatric patients with recurrent preauricular inflammation. The identification of a characteristic sinus orifice at the superior cartilaginous EAC during focused examination is diagnostic.

LEVEL OF EVIDENCE: Level 4.

Для цитирования: Luo Wenwei, Mao Weilong, Sheng Xiaoli, Xu Xianzhen, Xu Mimi, Chen Liangsi. Clinical Characteristics of a Rare Type I Congenital First Branchial Cleft Anomaly With Native Sinus Tract.. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 2025. DOI: 10.1097/mao.0000000000004691.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.