Chimelli L, Symon L, Scaravilli F
J Neuropathol Exp Neurol. 1984 Nov;43(6):634-42. doi: 10.1097/00005072-198411000-00007.
Granular cell tumors arising from the cranial nerves are rare. We describe a granular cell neoplasm of the fifth cranial nerve in a 66-year-old male. Light microscopic appearances included rows and clusters of cells with small peripheral nuclei and abundant eosinophilic cytoplasm. Ultrastructurally the cytoplasm of these cells contained numerous dense bodies, multivesicular bodies and vacuoles. In some areas tumor cells were intermingled with myelinated and unmyelinated nerve fibers showing the same relationships as do Schwann cells and nerve fibers. The association between tumor cells and axon seen in this case lends further support to the putative Schwann cell origin of this neoplasm.
起源于颅神经的颗粒细胞瘤很罕见。我们描述了一名66岁男性的第五颅神经颗粒细胞瘤。光镜下表现为细胞呈条索状和团块状,细胞核位于周边且小,细胞质嗜酸性丰富。超微结构显示这些细胞的细胞质内含有大量致密体、多囊体和空泡。在一些区域,肿瘤细胞与有髓和无髓神经纤维相互交织,其关系与施万细胞和神经纤维相同。本病例中所见的肿瘤细胞与轴突之间的关联进一步支持了该肿瘤起源于施万细胞的推测。