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Int J Surg Pathol ; 26(4): 364-369, 2018 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-29254456

RESUMO

Primary extraspinal myxopapillary ependymoma (MPE) is an exceptionally rare lesion that is mainly located in the subcutaneous sacrococcygeal region. We describe the first case of MPE that presented as an intramuscular tumor mass located in the lumbar area. Absence of the visible connection with the spinal cord and lack of any other tumors in the reported case argue for the primary ectopic origin of the MPE. The differential diagnosis of MPE is discussed. Additionally, we evaluated the expression level of molecular biomarkers that have a prognostic value in central nervous system tumors.


Assuntos
Ependimoma/genética , Ependimoma/patologia , Neoplasias de Tecidos Moles/genética , Neoplasias de Tecidos Moles/patologia , Adolescente , Feminino , Humanos , Região Lombossacral , Transcriptoma
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