Chitale A R, Murthy A K, Desai A P, Lalitha V S
Jaslok Hospital Research Centre, K.E.M. Hospital & Cancer Research Centre, Bombay, India.
Indian J Cancer. 1991 Mar;28(1):1-8.
This report deals with the ultrastructural observations of 30 peripheral nerve sheath tumours [PNST], which include 25 schwannomas of acoustic nerve, one schwannoma of cauda equina, one neurofibroma from a case of Von Recklinghausen's disease, one pigmented neurofibroma of spinal nerve root and a malignant schwannoma of frontal region. Interdigitating slender cytoplasmic processes covered with a continuous layer of basal lamina constitute the single most important ultrastructural attribute of Schwann cells. Myelin formation was encountered in the cell processes of four out of 25 acoustic schwannomas. In four cases Microtubular arrays identical to that in an axon were seen in Schwann cells. These two observations require further support by additional cases of PNST studies by electron microscopy. The neurofibroma consisted only of Schwann cells and no ultrastructurally identifiable perineurial cells or fibroblasts were detected. The cells in the pigmented neurofibroma revealed submicroscopic features of both Schwann cell and melanocyte, indicating their common ancestry. A unique case of malignant schwannoma arising from frontal meninges is illustrated and it is emphasized that electron microscopy is mandatory for a correct histogenetic diagnosis of malignant tumours which occur at unexpected anatomical sites.
本报告涉及30例周围神经鞘瘤[PNST]的超微结构观察,其中包括25例听神经鞘瘤、1例马尾神经鞘瘤、1例来自冯·雷克林豪森病患者的神经纤维瘤、1例脊神经根色素性神经纤维瘤以及1例额叶恶性神经鞘瘤。相互交错的细长细胞质突起覆盖着一层连续的基膜,这是施万细胞最重要的单一超微结构特征。25例听神经鞘瘤中有4例在细胞突起中观察到髓鞘形成。在4例中,施万细胞中可见与轴突中相同的微管排列。这两项观察结果需要通过对更多PNST病例进行电子显微镜研究来进一步证实。神经纤维瘤仅由施万细胞组成,未检测到超微结构可识别的神经束膜细胞或成纤维细胞。色素性神经纤维瘤中的细胞显示出施万细胞和黑素细胞的亚微观特征,表明它们有共同的起源。本文展示了1例起源于额叶脑膜的独特恶性神经鞘瘤病例,并强调电子显微镜对于正确诊断发生在意外解剖部位的恶性肿瘤的组织发生学至关重要。