Article Text
Abstract
Solitary neurofibromas of the larynx are extremely rare, with a total of 15 cases described in the literature. Nonetheless, acquaintance with this diagnosis is important, as misdiagnoses can have negative consequences. Presenting symptoms are non-specific and depend on tumour size and location. As well-defined submucosal masses with a broad differential diagnosis, they remain a clinical and radiological challenge. While some characteristics might favour a benign nature and subtle signs might help narrow the differential diagnosis, imaging alone is not sufficient for differentiation and definitive diagnosis requires a biopsy. Complete surgical resection and long-term follow-up is indicated. We share our experience on a case of a solitary laryngeal neurofibroma in a middle-aged woman, presenting with a large well-defined paraglottic lesion.
- ear
- nose and throat/otolaryngology
- head and neck cancer
- radiology
- head and neck surgery
- peripheral nerve disease
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Footnotes
Contributors BC: reviewed the subject, collected the images and wrote and reviewed the manuscript. RP: consulting surgeon responsible for the surgery, clinical management and follow-up of the patient and reviewed the manuscript. IF: made the pathologic diagnosis and reviewed all the pathology specimens available and reviewed the pathology part of the manuscript. AB: conceptualised the manuscript, reviewed the images and helped in writing and reviewing the manuscript.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Patient consent for publication Obtained.
Provenance and peer review Not commissioned; externally peer reviewed.