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电子显微镜检查在恶性神经鞘瘤诊断中的应用。6例报告。

Electron microscopy in the diagnosis of malignant schwannomas. A report of six cases.

作者信息

Chitale A R, Dickersin G R

出版信息

Cancer. 1983 Apr 15;51(8):1448-61. doi: 10.1002/1097-0142(19830415)51:8<1448::aid-cncr2820510819>3.0.co;2-p.

Abstract

The diagnosis of malignant schwannoma may be difficult or impossible by light microscopy alone, if the neoplasm is poorly differentiated and if there is no clinical evidence for its arising from a nerve-trunk. Six cases of malignant schwannoma in which electron microscopy confirmed or established the diagnosis are reported. In four cases, the anatomic origin of the neoplasm arising from a large nerve was demonstrated at the time of operation, and in one of these the patient had von Recklinghausen's disease. In three of the four cases, as well as in the fifth case, in which the tumor was associated with an overlying malignant melanoma, the distinctive schwannoma patterns of Antoni types A and B tissue were absent. In the sixth case, there were no clinical clues as to nerve sheath origin, but both the light and electron microscopic features of the neoplasm were very characteristic of Schwann cell derivation. The most consistently present, ultrastructural features of malignant schwannoma are the spindle shape of the cells and the terminal cytoplasmic processes. If the processes show intertwining and if lateral cell borders are interdigitated, the diagnosis is more readily confirmed. Likewise, basal lamina is an important diagnostic feature but may be scant and focal in the very cellular and less differentiated tumors. Microfilaments are usually present, albeit in varying numbers, and they do not form the dense bodies seen in smooth muscle cells. Other diagnostically useful, but less consistent characteristics include microtubules, primary and secondary lysosomes, and dense-core type granules. Long-spacing collagen was present in only one case and in none of those reviewed from the literature. This is also an important finding. It is probable that most malignant nerve sheath neoplasms arise from Schwann cells, rather than from fibroblasts or perinurial cells, but electron microscopy often will be necessary to confirm this impression.

摘要

仅通过光学显微镜检查,恶性神经鞘瘤的诊断可能困难甚至无法实现,尤其是肿瘤分化不良且无临床证据表明其起源于神经干时。本文报告了6例经电子显微镜检查确诊或明确诊断为恶性神经鞘瘤的病例。4例在手术时证实肿瘤起源于大神经,其中1例患者患有冯·雷克林豪森病。在这4例中的3例以及第5例中,肿瘤与上方的恶性黑色素瘤相关,均未出现典型的Antoni A型和B型神经鞘瘤组织模式。第6例中,没有关于神经鞘起源的临床线索,但肿瘤的光学显微镜和电子显微镜特征均非常符合施万细胞来源。恶性神经鞘瘤最常见的超微结构特征是细胞呈梭形以及细胞质有终末突起。如果突起相互缠绕且细胞侧面边界相互交错,则更易于确诊。同样,基底膜是一个重要的诊断特征,但在细胞密集且分化程度较低的肿瘤中可能稀少且呈局灶性。微丝通常存在,数量不等,且不会形成平滑肌细胞中所见的致密体。其他有助于诊断但不太一致的特征包括微管、初级和次级溶酶体以及致密核心型颗粒。仅1例出现长间距胶原,文献复习的病例中均未出现。这也是一个重要发现。大多数恶性神经鞘瘤可能起源于施万细胞,而非成纤维细胞或神经束膜细胞,但通常需要电子显微镜检查来证实这一推测。

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