Publicação

Rhabdoid choroid plexus carcinoma: a rare histological type

Ver documento

Detalhes bibliográficos
Resumo:Primary central nervous system atypical teratoid/rhabdoid tumors mostly occur during early childhood and are almost invariably fatal. These tumors show similar histological and radiological features to primitive neuroectodermal tumor, meduloblastoma and choroid plexus carcinoma, but present different biological behaviors. We present the case of an 18 year-old man who presented headache, vomiting and ataxia. CT-scan and MRI revealed a posterior fossa tumor. A gross total resection was performed. An intraoperative study showed papillary-like tumors with large cells and mitotic features. Histological examination showed two different main growth patterns: solid sheets of undifferentiated polygonal cells with papillary features and rhabdoid cells. Immunohistochemically, these rhabdoid cells were positive for vimentin, epithelial membrane antigen, smooth-muscle actin, cytokeratin, S-100 protein, and glial fibrillary acidic protein. Electro-microscopically, the typical rhabdoid cells contained whorled bundles of intermediate filaments in their cytoplasm. A rhabdoid tumor is a clinicalpathological entity and emphasizes the necessity to distinguish this unique tumor from other pediatric central nervous system neoplasms. Cytopathological features, immunohistochemistry and electro-microscopy differential diagnoses are discussed.
Autores principais:Tena-Suck,Martha Lilia
Outros Autores:Gómez-Amador,Juan Luis; Ortiz-Plata,Alma; Salina-Lara,C.; Rembao-Bojórquez,Daniel; Vega-Orozco,Rosalba
Assunto:choroid plexus tumors imunohistochemistry rhabdoid/teratoid tumor rhabdoid features rhabdoid carcinoma
Ano:2007
País:Brasil
Tipo de documento:artigo
Tipo de acesso:acesso aberto
Instituição associada:IBICT
Idioma:inglês
Origem:Oasisbr

Registos relacionados

Atividades financiadas

Não foram encontrados projetos financiados.

Registos relacionados