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Extranodal Marginal Zone B-Cell Lymphoma of Mucosa-Associated Tissue Type Involving the Dura / Journal of the Korean Cancer Association, 대한암학회지
Article em En | WPRIM | ID: wpr-132148
Biblioteca responsável: WPRO
ABSTRACT
Primary central nervous system marginal zone B-cell lymphoma (MZBCL) is very rare, with only a few reported cases worldwide. It has an indolent disease course with high cure potential. We experienced a rare case of dural MZBCL of mucosa-associated lymphoid tissue (MALT) in a 69-year-old man who presented with headache. A magnetic resonance imaging scan of brain showed a 1.9×3.6-cm-sized extra-axial mass with a broad based dural attachment to the anterosuperior aspect of the falx cerebri, radiographically consistent with meningioma. Surgical resection yielded a MZBCL of the MALT type. Histopathology revealed a lymphoplasmacytic infiltration of the dura, and immunohistochemical study showed a B-cell phenotype with CD20, bcl-2, MUM-1, Ki-67 positive. He was treated with chemotherapy after complete surgical resection and remained free of disease at 30 months after chemotherapy. MALT lymphoma must be considered in the differential diagnosis in patients presenting radiographically with meningioma.
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Texto completo: 1 Índice: WPRIM Assunto principal: Fenótipo / Encéfalo / Imageamento por Ressonância Magnética / Linfócitos B / Sistema Nervoso Central / Neoplasias do Sistema Nervoso Central / Linfoma de Zona Marginal Tipo Células B / Diagnóstico Diferencial / Tratamento Farmacológico / Dura-Máter Tipo de estudo: Diagnostic_studies Limite: Aged / Humans Idioma: En Revista: Cancer Research and Treatment Ano de publicação: 2016 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Assunto principal: Fenótipo / Encéfalo / Imageamento por Ressonância Magnética / Linfócitos B / Sistema Nervoso Central / Neoplasias do Sistema Nervoso Central / Linfoma de Zona Marginal Tipo Células B / Diagnóstico Diferencial / Tratamento Farmacológico / Dura-Máter Tipo de estudo: Diagnostic_studies Limite: Aged / Humans Idioma: En Revista: Cancer Research and Treatment Ano de publicação: 2016 Tipo de documento: Article