New classification and surgical strategy for work type I congenital first branchial cleft anomalies in children.


Journal

European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery
ISSN: 1434-4726
Titre abrégé: Eur Arch Otorhinolaryngol
Pays: Germany
ID NLM: 9002937

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 28 05 2023
accepted: 17 07 2023
medline: 2 11 2023
pubmed: 28 7 2023
entrez: 28 7 2023
Statut: ppublish

Résumé

To investigate the anatomical relationships between the structures adjacent to the cartilaginous portion of the ear canal in children with Work type I congenital branchial cleft anomalies (CFBCAs) and to develop new classifications and surgical strategies. Retrospective analysis was performed on 50 children with Work type I CFBCAs admitted between December 2018 and December 2022. Among the 50 children, total parotidectomy was performed on 49 sides. In 44 cases (88%), the main body of the lesion was closely associated with the cartilage of the inferior ear canal wall. Among these cases, the lesions in 40 cases occurred within the space enclosed by the dorsal inferior wall cartilage, mastoid process, and parotid gland, while in the remaining four cases, the lesions were located between the anterior inferior wall cartilage and parotid gland. Based on the preoperative imaging observations, clinical manifestations, and intraoperative findings, the cases were classified into 6 subtypes (a to f) including 21 cases (42%) of Type Ia (inferior wall of EAC), 7 cases (14%) of Type Ib (bottom wall of EAC), 12 cases (24%) of Type Ic (posterior-inferior wall of EAC), 4 cases (8%) of Type Id (anterior-inferior wall of EAC), 4 cases (8%) of Type Ie (anterior ear wall of EAC), and 2 cases (4%) of Type If (isolated from parotid). Surgical intervention is the only treatment for first branchial cleft anomalies and a comprehensive understanding of the classifications will help with the precise localisation and excision of the lesions.

Identifiants

pubmed: 37505262
doi: 10.1007/s00405-023-08140-4
pii: 10.1007/s00405-023-08140-4
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5539-5546

Subventions

Organisme : Innovative Research Group Project of the National Natural Science Foundation of China
ID : 82071038

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Références

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Auteurs

Jing Bi (J)

Department of ENT and Head & Neck Surgery, The Children's Hospital Zhejiang University School of Medicine, Binsheng Road 3333, Hangzhou, 310051, Zhejiang, China. bijing-ent@zju.edu.cn.

Bo Yu (B)

Department of ENT and Head & Neck Surgery, The Children's Hospital Zhejiang University School of Medicine, Binsheng Road 3333, Hangzhou, 310051, Zhejiang, China.

Yong Fu (Y)

Department of ENT and Head & Neck Surgery, The Children's Hospital Zhejiang University School of Medicine, Binsheng Road 3333, Hangzhou, 310051, Zhejiang, China.
Zhejiang Provincial Key Lab of Genetic and Developmental Disorder, Hangzhou, Zhejiang, China.

Bin Xu (B)

Department of ENT and Head & Neck Surgery, The Children's Hospital Zhejiang University School of Medicine, Binsheng Road 3333, Hangzhou, 310051, Zhejiang, China.

Yang Zhang (Y)

Department of ENT and Head & Neck Surgery, The Children's Hospital Zhejiang University School of Medicine, Binsheng Road 3333, Hangzhou, 310051, Zhejiang, China.

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