Título: TONGUE NEUROMA IN A PEDIATRIC PATIENT
Nome do Apresentador: Karine Duarte da Silva
Categoria do Trabalho: Painel de caso clínico (PCC)
Área Temática: Odontologia para pacientes especiais
Resumo: Neurofibromatosis (NF) are rare genetic diseases caused by pathogenic variants in certain genes, leading to a series of clinical manifestations such as neurofibromas. The most common type, NF1, is characterized by multiple neuromas anywhere on the body, brown stains, freckles in the axillary or inguinal regions, optic glioma, Lisch nodules, sphenoid dysplasia, and a dominant inheritance pattern. The case described here involves a 10-year-old male patient with NF1, whose parents and grandparents also had the same diagnosis. We observed intellectual deficit, scoliosis, kyphosis, café au lait spots all over the body, ephelides in the axilla and a significant neuroma on the tongue. Three partial glossectomies were performed (2016/2023/2024) to remove the neuroma. This case aims to describe the manifestations and alterations present and the follow-up by a multi-professional team.
Autor 1: Mariana Israel Rocha
E-mail 1: [email protected]
Autor 2: Karine Duarte da Silva
E-mail 2: [email protected]
Autor 3 : Juliani Santana de Oliveira
E-mail 3: [email protected]
Autor 4: Kelly Machado de Andrade e Reyes
E-mail 4: [email protected]
Autor 5: Ingrid Akemi Morita Kataguiri
E-mail 5: [email protected]
Autor 6: Tatiane Marega
E-mail 6: [email protected]
Autor 7: Silvana Ribeiro Roda
E-mail 7: [email protected]
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