Sanguinetti C, Greco F, de Palma L, Specchia N, Toesca A, Nori S
Cattedra di Traumatologia della Strada, Istituto di Clinica Ortopedica, Roma.
Ital J Orthop Traumatol. 1991 Jun;17(2):237-46.
An electron microscopic study of 4 solitary schwannomas and 2 neurofibromas of peripheral nerves was performed with the aim of investigating the debated histogenesis of the two types of lesion. Our observations confirm that solitary schwannoma is composed almost exclusively of cells with characteristics of differentiated Schwann cells, thus providing evidence for a neuroectodermal origin of the tumor. Analysis of the ultrastructure of neurofibroma shows the presence of 3 different types of cells: Schwann-like cells, perineurial-like cells, and fibroblast-like cells. Perineurial-like cells were prevalent in our observations. These findings as well as the many controversial aspects of the origin of neurofibroma could be explained by separating this type of neoplasia into two pathological forms: perineurial and interstitial. Moreover, the numerous differences between solitary schwannoma and neurofibroma allow us to hypothesize a different cellular origin for each tumor. If confirmed by further observations, this would explain the difference in the capacity of the two types of neoplasia to undergo malignant change, an occurrence almost unknown in solitary schwannoma yet relatively common in neurofibroma.
为研究两种病变存在争议的组织发生学,对4例孤立性神经鞘瘤和2例周围神经神经纤维瘤进行了电子显微镜研究。我们的观察证实,孤立性神经鞘瘤几乎完全由具有分化型施万细胞特征的细胞组成,从而为该肿瘤的神经外胚层起源提供了证据。对神经纤维瘤超微结构的分析显示存在3种不同类型的细胞:施万样细胞、神经束膜样细胞和成纤维细胞样细胞。在我们的观察中,神经束膜样细胞最为常见。将这种类型的肿瘤形成分为两种病理形式:神经束膜型和间质型,可以解释这些发现以及神经纤维瘤起源的许多争议方面。此外,孤立性神经鞘瘤和神经纤维瘤之间的众多差异使我们能够推测每种肿瘤有不同的细胞起源。如果进一步的观察证实这一点,这将解释两种肿瘤形成发生恶变能力的差异,孤立性神经鞘瘤几乎不会发生恶变,而神经纤维瘤则相对常见。