Neurofibromatosis type I with an Rare Oral Manifestation

Neurofibromatosis type I is one of the most common genetic diseases and it may have oral manifestation. Objetive: To report a case about a 33 years old female patient diagnosed with neurofibromatosis type I in the skin. Case Report: In the extraoral clinical examination were observed subcutaneous nodules and café-au-lait spots, in different sizes around the body. In the intraoral examination was diagnosed the presence of rounded nodule in the hard palate. The excisional biopsy of the lesion was performed and the histopathological examination suggested a diagnosis of neurofibroma. Conclusion: The case report emphasizes the importance of a detailed anamnesis and a thorough physical examination, so that systemic diseases can be considered in oral diagnosis.