Miller R L, Burzynski N J, Giammara B L
J Oral Pathol. 1977 Sep;6(5):253-63. doi: 10.1111/j.1600-0714.1977.tb01647.x.
The ultrastructure of oral neuromas from 2 patients with multiple mucosal neuromas, pheochromocytoma, medullary thyroid carcinoma syndrome reveals numerous hypertrophic unmyelinated and myelinated axons, hyperplastic neurilemmal cells and associated collagen fiber formation. These tumors are described and compared ultrastructurally with neurilemmomas and neurofibromas as described by other authors. On the basis of this comparison, these tumors are not considered to be of neurilemmal origin. On the basis of light and electron microscopic histology it is postulated that these tumors represent hypertrophy of axons similar to that noted in amputation neuromas.
对2例患有多发性黏膜神经瘤、嗜铬细胞瘤、甲状腺髓样癌综合征患者的口腔神经瘤进行超微结构研究,发现有大量肥大的无髓鞘和有髓鞘轴突、增生的神经膜细胞以及相关胶原纤维形成。本文对这些肿瘤进行了描述,并在超微结构上与其他作者所描述的神经鞘瘤和神经纤维瘤进行了比较。基于这种比较,这些肿瘤不被认为起源于神经膜。根据光镜和电镜组织学推测,这些肿瘤代表轴突肥大,类似于截肢神经瘤中所观察到的情况。