Kornfeld M
J Neuropathol Exp Neurol. 1986 Jul;45(4):447-62.
Granular cell tumors in the cerebral hemispheres are rare and of unknown origin. Two large aggressive cerebral neoplasms composed mainly of granular cells and also containing neoplastic astrocytes were studied histologically, ultrastructurally and immunohistochemically. In both instances, transitional forms between astrocytes and typical granular cells were demonstrated. In the second case which consisted of a central core of typical glioblastoma surrounded by a thick shell of granular cells, the latter spread in a fashion that is characteristic of intrinsic tumors of the central nervous system by forming abundant secondary structures of Scherer, particularly under the pia and around cortical blood vessels. All the evidence indicates that in these two cases granular cells were transformed neoplastic astrocytes. Paradoxically, many granular cells exhibited benign cytological features that belied their malignant nature.
大脑半球的颗粒细胞瘤很罕见,其起源不明。对两个主要由颗粒细胞组成且还含有肿瘤性星形胶质细胞的大型侵袭性脑肿瘤进行了组织学、超微结构和免疫组织化学研究。在这两个病例中,均证实了星形胶质细胞与典型颗粒细胞之间的过渡形式。在第二个病例中,由典型胶质母细胞瘤的中央核心被一层厚厚的颗粒细胞壳包围,后者以中枢神经系统固有肿瘤的特征性方式扩散,形成大量的谢勒二级结构,尤其是在软脑膜下和皮质血管周围。所有证据表明,在这两个病例中,颗粒细胞是转化的肿瘤性星形胶质细胞。矛盾的是,许多颗粒细胞表现出良性的细胞学特征,掩盖了它们的恶性本质。