Hilbig Arlete, Barbosa-Coutinho Lígia Maria, Toscani Nadima, Ribeiro Marlise de Castro, da Cunha Bartira Silveira Campos
Department of Morphological Sciences, Fundação Faculdade Federal de Ciências Médicas de Porto Alegre, UFRGS, Rua Sarmento Leite 245, 90050-170 Porto Alegre RS, Brazil.
Arq Neuropsiquiatr. 2006 Sep;64(3B):781-6. doi: 10.1590/s0004-282x2006000500015.
Gliomatosis cerebri (GC) is a rare form of CNS neoplasia in which there is diffuse involvement of the nervous tissue with or without the presence of tumor mass. The origin of the tumor is unknown, nor whether it represents a disease with diffuse onset or infiltration from a neoplastic focus. Here we studied the histopathologic characteristics of 6 cases with a diagnosis of GC and performed an immunohistochemical analysis using glial fibrillary acidic protein (GFAP), synaptophysin, nestin and vimentin. Most tumor cells were negative for GFAP, even though there were foci of positivity for this marker in all cases. We detected the presence of many positive cells for nestin and vimentin in all studied samples. The presence of these cells may indicate origin of the tumor from undifferentiated cells with a high degree of mobility.
大脑胶质瘤病(GC)是一种罕见的中枢神经系统肿瘤形成形式,其中神经组织存在弥漫性受累,伴有或不伴有肿瘤块。肿瘤的起源尚不清楚,也不清楚它是代表一种弥漫性发病的疾病还是从肿瘤病灶浸润而来。在这里,我们研究了6例诊断为GC的组织病理学特征,并使用胶质纤维酸性蛋白(GFAP)、突触素、巢蛋白和波形蛋白进行了免疫组织化学分析。大多数肿瘤细胞对GFAP呈阴性,尽管在所有病例中都有该标志物的阳性灶。我们在所有研究样本中检测到许多巢蛋白和波形蛋白阳性细胞。这些细胞的存在可能表明肿瘤起源于具有高度迁移性的未分化细胞。