First branchial cleft anomalies in children: long-term outcome in 16 patients.

IF 1.9 3区 医学 Q2 OTORHINOLARYNGOLOGY
M Moyaert, K Vandermaesen, Q-A Parys, P Delaere, J Meulemans, G Hens, R Hermans, V Vander Poorten
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引用次数: 0

Abstract

Introduction: 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.

Methods: 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.

Results: 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.

Conclusion: 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.

儿童第一鳃裂异常:16例患者的长期预后。
简介:第一鳃裂畸形是一种罕见的先天性头颈部畸形,常被误诊和误治。我们将介绍FBCA的临床表现、诊断、围手术期与面神经的关系、手术入路、并发症和患者满意度。方法:对1999年至2021年间接受FBCA手术治疗的16例连续队列患者进行分析。从他们的医疗记录中提取人口统计和临床信息。此外,通过电话访谈14例患者,使用李克特量表评估术后结果和患者满意度。结果:16例患者(女11例,男5例)手术治疗,年龄7个月~ 13岁。I型和II型FBCA分布均匀。病变表现为囊肿(n = 4)、鼻窦(n = 7)或瘘管(n = 5)。主要症状为肿胀、炎症和分泌物。有耳科症状的占31%。在80%的患者中,需要磁共振成像才能达到正确的诊断。10例患者(63%)在本中心接受最终手术治疗前曾在其他中心尝试过手术。所有患者均完成了完全切除。术后并发症包括局限性Frey综合征(n = 4)、暂时性增生性瘢痕(n = 4)、面神经下颌缘支轻度麻痹(n = 1)和局限性外耳道狭窄(n = 1)。一名患者在外耳道水平复发,需要进行小翻修手术。患者平均满意度为13.64分(满分15分)。结论:充分的临床检查、对不同实体的认识和对专家头颈部放射学建议的认识对FBCA的正确诊断和分型,确定正确的手术入路至关重要。诊断为FBCA的患者在专业中心接受手术是至关重要的。尽管具有挑战性的手术及其潜在的并发症,总体上病人的满意度仍然很高。
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来源期刊
CiteScore
5.30
自引率
7.70%
发文量
537
审稿时长
2-4 weeks
期刊介绍: Official Journal of European Union of Medical Specialists – ORL Section and Board Official Journal of Confederation of European Oto-Rhino-Laryngology Head and Neck Surgery "European Archives of Oto-Rhino-Laryngology" publishes original clinical reports and clinically relevant experimental studies, as well as short communications presenting new results of special interest. With peer review by a respected international editorial board and prompt English-language publication, the journal provides rapid dissemination of information by authors from around the world. This particular feature makes it the journal of choice for readers who want to be informed about the continuing state of the art concerning basic sciences and the diagnosis and management of diseases of the head and neck on an international level. European Archives of Oto-Rhino-Laryngology was founded in 1864 as "Archiv für Ohrenheilkunde" by A. von Tröltsch, A. Politzer and H. Schwartze.
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