Goates J J, Dickson D W, Horoupian D S
Department of Pathology/Neuropathology, Stanford University School of Medicine, CA 94305-5324.
Acta Neuropathol. 1991;82(6):527-32. doi: 10.1007/BF00293390.
Meningioangiomatosis (MA) is a rare malformative lesion of the central nervous system. It has generally been thought that the main cells forming this lesion are derived from arachnoidal cap cells. We report a case of MA in which histochemical, immunoperoxidase and electron microscopic studies did not support a meningothelial origin of this lesion. Rather, the lesion in this case appears to be a vascular malformation with the dominant cells being fibroblastic, derived from vessel walls; however, their origin from arachnoid cap cells that differentiated into fibroblast-like cells could not be totally ruled out. Residual neurons within the lesion contained neurofibrillary tangles with ultrastructural and immunostaining properties identical to those seen in Alzheimer's disease except for the absence of A4 amyloid.
脑膜血管外皮细胞瘤(MA)是一种罕见的中枢神经系统发育异常性病变。一般认为形成该病变的主要细胞来源于蛛网膜帽状细胞。我们报告一例MA病例,其组织化学、免疫过氧化物酶和电子显微镜研究并不支持该病变起源于脑膜内皮细胞。相反,该病例中的病变似乎是一种血管畸形,主要细胞为成纤维细胞,来源于血管壁;然而,也不能完全排除它们起源于分化为成纤维细胞样细胞的蛛网膜帽状细胞。病变内的残留神经元含有神经原纤维缠结,其超微结构和免疫染色特性与阿尔茨海默病所见相同,但无A4淀粉样蛋白。