RESUMO
A 59-year-old woman presented with disturbance of consciousness and decreased visual acuity caused by a suprasellar mass identified on MRI. A bifrontal interhemispheric approach allowed removal of the top and lateral sides of the tumor from the wall of the third ventricle. The hypothalamus appeared to be the origin of the mass, which proved to be hemangioblastoma, a rare tumor in this location.
Assuntos
Neoplasias do Ventrículo Cerebral/patologia , Hemangioblastoma/patologia , Neoplasias Hipotalâmicas/patologia , Hipotálamo/patologia , Terceiro Ventrículo/patologia , Antígenos CD34/análise , Antígenos CD34/metabolismo , Biomarcadores Tumorais , Capilares/patologia , Neoplasias do Ventrículo Cerebral/irrigação sanguínea , Neoplasias do Ventrículo Cerebral/cirurgia , Transtornos da Consciência/etiologia , Feminino , Hemangioblastoma/irrigação sanguínea , Hemangioblastoma/cirurgia , Humanos , Neoplasias Hipotalâmicas/irrigação sanguínea , Neoplasias Hipotalâmicas/cirurgia , Imageamento por Ressonância Magnética , Pessoa de Meia-Idade , Procedimentos Neurocirúrgicos , Molécula-1 de Adesão Celular Endotelial a Plaquetas/análise , Molécula-1 de Adesão Celular Endotelial a Plaquetas/metabolismo , Sela Túrcica/anatomia & histologia , Células Estromais/patologia , Terceiro Ventrículo/cirurgia , Resultado do Tratamento , Baixa Visão/etiologiaRESUMO
OBJECT: The authors' aim in conducting this study was to investigate retrospectively the prognostic significance of angiogenic features in optic pathway/hypothalamic gliomas (OPHGs) in children. METHODS: Patients were identified in whom a diagnosis of OPHG was made using pathological analysis at the Toronto Hospital for Sick Children between 1985 and 2002. Tumor specimens were reviewed for diagnostic accuracy and adequacy of the specimen. Sections were immunostained with factor VIII to assess microvessel density (MVD). A ratio of alpha-smooth muscle actin to factor VIII immunostaining was calculated to arrive at a vascular maturity index (VMI). Vascular endothelial growth factor (VEGF) and VEGF receptor (VEGFR) immunostaining were performed to evaluate angiogenic factors. In addition, the MIB-1 labeling index (LI) was used to assess proliferation. These factors were evaluated with respect to progression-free survival (PFS). Forty-one of 60 patients originally identified had adequate samples and follow up for inclusion in the study. Of these, eight patients had coexisting neurofibromatosis Type 1. Twenty-eight patients experienced tumor progression after the initial treatment (surgery with or without adjuvant treatment). Thirty-eight patients are still alive. A high MVD (> 21 vessels/1.2 mm2) was associated with a significantly higher rate of progression compared with a low MVD (< 21 vessels/1.2 mm2; p = 0.017). Microvessel density was also predictive of reduced PFS on multivariate analysis stratified for extent of resection (p = 0.04), and VMI as well as intensity and distribution of VEGF and VEGFR staining and the MIB-1 LI were not significantly associated with PFS. CONCLUSIONS: These findings suggest that MVD is the best current predictor of PFS in incompletely resected OPHGs. This information highlights the importance of angiogenesis in regard to low-grade gliomas.
Assuntos
Neoplasias Hipotalâmicas/irrigação sanguínea , Neovascularização Patológica/patologia , Glioma do Nervo Óptico/irrigação sanguínea , Adolescente , Biomarcadores Tumorais/análise , Divisão Celular/fisiologia , Criança , Pré-Escolar , Progressão da Doença , Humanos , Neoplasias Hipotalâmicas/patologia , Neoplasias Hipotalâmicas/cirurgia , Técnicas Imunoenzimáticas , Lactente , Microcirculação/patologia , Neoplasia Residual/irrigação sanguínea , Neoplasia Residual/patologia , Neovascularização Patológica/cirurgia , Glioma do Nervo Óptico/patologia , Glioma do Nervo Óptico/cirurgia , Prognóstico , Estudos RetrospectivosRESUMO
We report five cases of tumors occurring in three children and in two adults. The tumors had unusual histomorphology and a mixture of ependymal and piloid-like astrocytic features and a myxoid stroma similar to myxopapillary ependymomas. MR imaging in three of the cases showed aggressive, intensely enhancing partially cystic hypothalamic-suprasellar masses near midline and near the floor of the third ventricle. In the three pediatric cases, the tumor encased the circle of Willis. This newly characterized tumor, the tanycytoma, has neoplastic cells with histomorphologic and ultrastructural characteristics similar to those of the tanycyte.