Hostname: page-component-745bb68f8f-hvd4g Total loading time: 0 Render date: 2025-02-11T13:49:16.788Z Has data issue: false hasContentIssue false

Neurofibroma of the supraglottic larynx in childhood

Published online by Cambridge University Press:  29 June 2007

Jenö Czigner*
Affiliation:
Clinic of Otolaryngology, Albert Szent-Györgyi Medical University, Szeged, Hungary.
Gabriella Fekete-Szabó
Affiliation:
Clinic of Otolaryngology, Albert Szent-Györgyi Medical University, Szeged, Hungary.
*
Jenö Czigner, M.D., A. Szent-Györgyi Medical University, Clinic of Otolaryngology, Tisza L. Krt. 111, H-6725 Szeged, Hungary.
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

The case of a male child with a benign neurogenic laryngeal tumour caused by von Recklinghausen's disease is presented. At the age of eight years, tracheostomy was necessary. The tumour, deforming the right half of the larynx and extending into the right half of the neck, was removed three years later. Following this procedure, decannulation was possible, and the patient has been free of laryngological complaints for six years.

Attention is drawn to the fact that autosomal dominantly inherited neurofibromatosis is a generalized benign tumour with a special form. If it involves any vital structure or forms a functional obstacle, meticulous surgical removal is necessary, and this provides good prospects over a long period.

Type
Clinical Records
Copyright
Copyright © JLO (1984) Limited 1994

References

Barker, V. (1987) Gene for von Recklinghausen's neurofibromatosis is in the pericentromeric region on chromosome 17. Science 236: 11001102.CrossRefGoogle ScholarPubMed
Chang-Lo, M. (1977) Laryngeal involvement in von Recklinghausen's disease: a case report and review of the literature. Laryngoscope 87: 435442.CrossRefGoogle ScholarPubMed
Daly, J. F., Roesler, H. G. (1963) Neurilemmoma of the cervical sympathetic chain. Archives of Otolaryngology 11: 262267.CrossRefGoogle Scholar
Holt, R. G. (1978) ENT manifestations of von Recklinghausen's disease. Laryngoscope 88: 16271632.CrossRefGoogle ScholarPubMed
Karja, J. (1982) Benign neoplastic tumours and space-occupying tumorous lesions of the larynx in children. Acta Otolaryngology 386 (Suppl.): 181183.CrossRefGoogle Scholar
Kimmelman, Ch. P. (1979) Otolaryngologic aspects of neurofibromatosis. Archives of Otolaryngology 105: 732736.CrossRefGoogle ScholarPubMed
McKennan, M. D., Bard, M. D. (1991) Neurofibromatosis type 2. Laryngoscope 101: 109113.CrossRefGoogle ScholarPubMed
Rees, G. (1971) Neurofibroma of the recurrent laryngeal nerve. Chest 60: 414418.CrossRefGoogle ScholarPubMed
Ruckley, R. W. (1986) Neurofibroma of the cervical sympathetic chain presenting with Homer's syndrome. Journal of Laryngology and Otology 100: 14331436.CrossRefGoogle Scholar
Seizinger, B. R., Roullau, G. A. (1987) Genetic linkage of von Rechlinghausen's neurofibromatosis to the nerve growth factor receptor gene. Cell 49: 589594.CrossRefGoogle Scholar
White, K., Bigler, C. R. (1986) Head and neck manifestations of neurofibromatosis. Laryngoscope 96: 732737.CrossRefGoogle ScholarPubMed