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BMJ Case Reports 2012; doi:10.1136/bcr.12.2011.5389
  • Rare disease

Intraoral schwannoma – a report of two cases

  1. Preeti P Nair3
  1. 1Oral Medicine & Radiology Department, Amrita School of Dentistry, Kochi, Kerala, India
  2. 2Head & Neck Institute, Amrita Institute of Medical Sciences, Kochi, India
  3. 3Oral Medicine & Radiology Department, People’s College of Dental Sciences & Research Centre, Bhopal, India
  1. Correspondence to Professor Preeti P Nair, shajihoss{at}gmail.com

Summary

Schwannomas, also known as neurilemmomas, are uncommon neoplasms, derived from schwann cells. These neoplasms, although rare, should be considered in the differential diagnosis of slow growing tumour masses of the oral cavity. The growth of these tumours sometimes causes displacement and compression of the nerve of origin, giving rise to clinical signs and symptoms. It can develop at any age and there is no sex predilection. Intraorally, the tongue is the most common site followed by the palate, floor of the mouth, buccal mucosa, lips and jaws. Surgical excision is the treatment of choice for schwannomas, with few reports of recurrence or malignant transformation. In this paper, the authors report two cases of patients with intraoral schwannoma, where the preoperative clinical diagnosis was inconclusive and final diagnosis was established based on radiographic and histopathological examination.

Footnotes

  • Competing interests None.

  • Patient consent Obtained.

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