SOLITARY FIBROUS TUMOR OF THE BRAIN: A CASE REPORT: TUMOR FIBROSO SOLITARIO CEREBRAL: A PROPÓSITO DE UN CASO

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Introduction: Solitary fibrous tumors (SFTs) are rare mesenchymal neoplasms that, although typically develop in the visceral pleura, occasionally occur in the intracranial cavity. Furthermore, they are characterized by high rates of metastasis and recurrence.Case Report: We present the case of a 59-...

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Detalles Bibliográficos
Autores: Ortiz Ramos, Valeria Antuanne, Itusaca Dueñas, Nora Nicole, Ulloa Ordoñez, Lucia Victoria, Paredes Pacual, Ricardo Romulo, Vela Ruiz , José Manuel, Yovera Orellana, Leslie Estefany, Torres Canqui, Jonathan Joel
Formato: artículo
Fecha de Publicación:2024
Institución:Universidad Ricardo Palma
Repositorio:Revistas - Universidad Ricardo Palma
Lenguaje:español
inglés
OAI Identifier:oai:oai.revistas.urp.edu.pe:article/6050
Enlace del recurso:http://revistas.urp.edu.pe/index.php/RFMH/article/view/6050
Nivel de acceso:acceso abierto
Materia:Solitary Fibrous Tumors
Brain Neoplasms
Central Nervous System Neoplasms
Tumores Fibrosos Solitarios
Neoplasias Encefálicas
Neoplasias del Sistema Nervioso Central
Descripción
Sumario:Introduction: Solitary fibrous tumors (SFTs) are rare mesenchymal neoplasms that, although typically develop in the visceral pleura, occasionally occur in the intracranial cavity. Furthermore, they are characterized by high rates of metastasis and recurrence.Case Report: We present the case of a 59-year-old male patient with a 3-month history of headache and bradyphrenia. Computed tomography revealed a neoformative tumor infiltrating the nasal cavity, ethmoid sinuses, and anterior cranial fossa, involving the left frontal lobe. The patient underwent two exploratory craniectomies, during which diagnoses suggestive of high-grade glial neoplasia and SFT were made. For precise diagnosis, immunohistochemistry was performed, which was consistent with solitary fibrous tumor. The case is analyzed, focusing particularly on histopathological aspects, the unusual location of this tumor, and its variable clinical manifestations.
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