Sarmento Dmitry José de Santana, Carvalho Sérgio Henrique Gonçalves de, Araújo José Cadmo Wanderley Peregrino de, Carvalho Marianne de Vasconcelos, Silveira Éricka Janine Dantas da
Department of Oral Pathology, Universidade de São Paulo (USP) - São Paulo (SP), Brazil.
Department of Odontology, Universidade Estadual da Paraíba (UEPB) - Araruna (PB), Brazil.
An Bras Dermatol. 2017 Mar-Apr;92(2):249-252. doi: 10.1590/abd1806-4841.20175277.
We report a 35-year-old mulatto female patient with neurofibromatosis Type 1 who presented with facial asymmetry. The patient had two lesions: florid cemento-osseous dysplasia associated with peripheral giant cell granuloma. She was referred for surgical treatment of the peripheral giant cell granuloma and the florid cemento-osseous dysplasia was treated conservatively by a multidisciplinary team. So far, no changes have been observed in the patient's clinical status. We observed no recurrence of peripheral giant cell granuloma. To the best of our knowledge, the present case is the first report of a patient with neurofibromatosis Type 1 associated with a giant cell lesion and florid cemento-osseous dysplasia.