NEUROFIBROMATOSIS TYPE I WITH INTRAORAL MANIFESTATION

Authors

  • Karla Coelho de Miranda Freitas
  • George João Ferreira do Nascimento
  • Richard Ribeiro Alonso de Andrade
  • Emanuel Dias
  • Belmiro Cavalcanti do Egito Vasconcelos
  • Ana Paula Veras Sobral

Keywords:

mouth, von Recklinghausen's diseases, neurofibroma, neurofibromatosis

Abstract

Neurofibromatosis type I is the most common clinicai variant of a group of genetic disorders known as neurofibromatosis that primarily affects the ce/1 growth of neural tissues. The purpose of this work is to describe one case of a woman with neurofibromatosis type I presenting oral cavity involvement. The clinica/ signs of the patient fulfilled the National lnstitute of Health criteria for neurofibromatosis type I and the intraoral-nodular lesion was removed, analyzed microscopically, and after H&E staining and S-100 immunohistochemical assay, the diagnosis of neurofibroma was confirmed. After two months, this intraoral lesion recurred.

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References

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Published

2006-02-28

How to Cite

Freitas, K. C. de M., Nascimento, G. J. F. do, Andrade, R. R. A. de, Dias, E., Vasconcelos, B. C. do E., & Sobral, A. P. V. (2006). NEUROFIBROMATOSIS TYPE I WITH INTRAORAL MANIFESTATION. Revista De Ciências Médicas, 15(1). Retrieved from https://seer.sis.puc-campinas.edu.br/cienciasmedicas/article/view/1138

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