Friede R L, Yasargil M G
J Neuropathol Exp Neurol. 1977 Sep-Oct;36(5):769-82. doi: 10.1097/00005072-197709000-00001.
A classification of granular cell lesions of neuropathologic interest is presented along with an unique case in which a suprasellar neoplasm having light and electron microscopic features of a meningioma contained multifocal nests of granular cells which apparently persisted in this tumor over a period of nearly five years. A spectrum of cell differentiation suggested the development of granular cells from small, electron-dense mesenchymal elements having numerous mitochondria. No evidence for a Schwann cell origin was found. It is proposed that the pituitary-hypothalamic axis, where intracranial granular cell nests and granular cell tumors are most common may also give origin to rare mixed neoplasms with a granular cell component.
本文提出了一种具有神经病理学意义的颗粒细胞病变分类方法,并介绍了一个独特病例。该病例中,鞍上肿瘤具有脑膜瘤的光镜和电镜特征,其中包含多灶性颗粒细胞巢,这些颗粒细胞巢在近五年的时间里明显持续存在于肿瘤中。一系列细胞分化情况表明,颗粒细胞由具有大量线粒体的小的、电子致密的间充质成分发育而来。未发现支持雪旺细胞起源的证据。有人提出,颅内颗粒细胞巢和颗粒细胞瘤最常见的垂体-下丘脑轴,也可能产生罕见的具有颗粒细胞成分的混合性肿瘤。