Moyaert M, Vandermaesen K, Parys Q-A, Delaere P, Meulemans J, Hens G, Hermans R, Vander Poorten V
Otorhinolaryngology, Head and Neck Surgery, University Hospitals Leuven, Leuven, Belgium.
Department of Oncology, Section Head and Neck Oncology, KU Leuven, Leuven, Belgium.
Eur Arch Otorhinolaryngol. 2025 Jun;282(6):3151-3161. doi: 10.1007/s00405-025-09203-4. Epub 2025 Jan 30.
First branchial cleft anomalies (FBCA) are rare congenital head and neck malformations, often subject to incorrect diagnosis and treatment. We present our experience with FBCA, focusing on clinical presentation, diagnosis, perioperative relation to the facial nerve, surgical approach, complications and patient satisfaction.
A consecutive cohort of 16 patients undergoing surgical treatment for FBCA between 1999 and 2021 was analyzed. Demographic and clinical information was extracted from their medical records. Additionally 14 patients were interviewed by telephone to assess postoperative outcomes and patient satisfaction using a Likert scale.
Sixteen patients (11 females, 5 males) were surgically treated at an age ranging from 7 months to 13 years. Type I and type II FBCA were evenly distributed. Lesions presented as cysts (n = 4), sinuses (n = 7) or fistulas (n = 5). The main symptoms were swelling, inflammation and discharge. Otologic symptoms were present in 31%. In 80% of patients, magnetic resonance imaging was needed to reach the correct diagnosis. Ten patients (63%) had a history of a surgical attempt in another center before definitive surgical treatment in our center. Complete excision was accomplished in all patients. Postoperative complications included limited Frey syndrome (n = 4), temporary hypertrophic scarring (n = 4), minimal paresis of the marginal mandibular branch of the facial nerve (n = 1) and limited external auditory canal stenosis (n = 1). One patient experienced a recurrence at the level of the external auditory canal, that required minor revision surgery. The average patient satisfaction score was 13.64 out of 15.
Thorough clinical examination, awareness of the different entities and awareness of expert head and neck radiological advice are crucial for correct FBCA diagnosis and typing, determining the correct surgical approach. It is crucial that patients diagnosed with FBCA undergo surgery in specialized centers. Despite the challenging surgery and its potential complications, the overall patient satisfaction remains high post- treatment.
第一鳃裂畸形(FBCA)是一种罕见的先天性头颈部畸形,常常容易被误诊和误治。我们介绍我们在FBCA方面的经验,重点关注临床表现、诊断、与面神经的围手术期关系、手术方法、并发症及患者满意度。
分析了1999年至2021年间连续接受FBCA手术治疗的16例患者。从他们的病历中提取人口统计学和临床信息。此外,通过电话采访了14例患者,使用李克特量表评估术后结果和患者满意度。
16例患者(11例女性,5例男性)接受了手术治疗,年龄从7个月至13岁不等。I型和II型FBCA分布均匀。病变表现为囊肿(n = 4)、窦道(n = 7)或瘘管(n = 5)。主要症状为肿胀、炎症和分泌物。31%的患者有耳部症状。80%的患者需要磁共振成像才能做出正确诊断。10例患者(6