Tsuneyoshi M, Enjoji M
Acta Pathol Jpn. 1979 May;29(3):363-75. doi: 10.1111/j.1440-1827.1979.tb00194.x.
A clinicopath-logic and electron microscopic study was performed on 35 cases of primary malignant peripheral nerve tumors, among which 12 developed in association with neurofibromatosis (von Recklinghausen's disease) and further 11 in keeping with anatomically discernible nerves in patients without neurofibromatosis. Depending upon the histologically predominant pattern, these tumors were subdivided into three groups: 23 compact spindle cell, 6 myxoid, and 6 epithelioid varieties of the tumor. The common ultrastructures in three of the 35 tumors were as follows: 1) The cell membranes manifested characteristic infoldings and lamellar configuation. 2) The tumor cell surfaces were coated by occasional basal lamina or homogeneously electron-dense membranous material. 3) The cytoplasms contained well-developed organelles and a few neurosecretory-type granules. Differential points from other soft-tissue sarcomas were briefly discussed on the histologic basis.
对35例原发性恶性周围神经肿瘤进行了临床病理及电子显微镜研究,其中12例与神经纤维瘤病(冯·雷克林豪森病)相关,另有11例发生于无神经纤维瘤病患者且与解剖学上可辨别的神经有关。根据组织学上的主要模式,这些肿瘤被分为三组:23例致密梭形细胞型、6例黏液样型和6例上皮样型肿瘤。35例肿瘤中的3例的常见超微结构如下:1)细胞膜表现出特征性的内褶和板层结构。2)肿瘤细胞表面偶尔有基底膜或均匀电子致密的膜性物质覆盖。3)细胞质中含有发育良好的细胞器和一些神经分泌型颗粒。在组织学基础上简要讨论了与其他软组织肉瘤的鉴别要点。