Case Report: Laryngeal web in a Yorkshire Terrier
- PMID: 40761841
- PMCID: PMC12320528
- DOI: 10.3389/fvets.2025.1595548
Case Report: Laryngeal web in a Yorkshire Terrier
Abstract
The laryngeal web is a congenital or acquired, abnormal transverse membrane, most commonly between the free edges of the vocal cords. Ensuing glottic stenosis may be asymptomatic or, in some cases, can lead to vocal and respiratory signs, such as dysphonia, stridor, and dyspnoea. Here, we describe a rare case of a laryngeal web in a Yorkshire Terrier presented with atypical clinical signs, including dysphonia, flatulence, and halitosis. Following a reasonable exclusion of an initial concern of laryngeal neoplasia and given the diagnosis of a congenital laryngeal web, the owners elected not to pursue surgical treatment. The dog's clinical signs remained unchanged with no development of new respiratory signs for over 4 years post-diagnosis. The findings presented herein highlight the importance of considering the laryngeal web as a rare but possible differential diagnosis for dysphonia and emphasise the need to establish specific individual selection criteria for surgical and medical treatments for dogs affected with this laryngeal anomaly.
Keywords: airways; congenital; dog; laryngeal web; larynx; ventriculocordectomy.
Copyright © 2025 Louie, Acosta, Yeadon and Bęczkowski.
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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References
-
- Burns H. Laryngeal webs (Chapter 4) in Laryngology: A Case-Based Approach. Plural Publishing, Incorporated. (2019).
-
- Holinger PH. Clinical aspects of congenital anomalies of the larynx, trachea, bronchi and oesophagus. J Laryngol Otol. (1961) 75:1–44. - PubMed
-
- Torres JBM, Lingan MB, Nieves CS, Reala ET. A makeshift stent using feeding port of siliconized nasogastric tube for management of idiopathic acquired supraglottic web. Otolaryngol Case Rep. (2025) 34:100648. doi: 10.1016/j.xocr.2024.100648 - DOI
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