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中枢神经细胞瘤的分化模式。11例活检组织的免疫组织化学研究。

Patterns of differentiation in central neurocytoma. An immunohistochemical study of eleven biopsies.

作者信息

von Deimling A, Janzer R, Kleihues P, Wiestler O D

机构信息

Abteilung für Neuropathologie, Universität Zürich, Switzerland.

出版信息

Acta Neuropathol. 1990;79(5):473-9. doi: 10.1007/BF00296105.

Abstract

Central neurocytoma has been characterised by its intraventricular localisation, predominant occurrence in young adults, oligodendroglioma-like histology, benign course and ultrastructural evidence for neuronal differentiation. Eleven intraventricular central neurocytomas were studied histopathologically, employing cell type-specific immunocytochemical markers and electron microscopic analysis. In the past, these lesions have caused diagnostic problems since central neurocytomas share basic histopathological features with other periventricular neoplasms. Accordingly, several tumours of this series had previously been classified as ependymomas of the foramen of Monro or oligodendrogliomas. Although generally regarded as benign lesions, two central neurocytomas of this series showed histopathological evidence of anaplasia, with focal necrosis, mitotic activity and vascular proliferation. All central neurocytomas exhibited immunoreactivity for neuron-specific enolase and synaptophysin, indicating consistent neuronal differentiation. Three tumours were studied by electron microscopy and contained synaptic vesicles, neuritic processes and neurosecretory granules. In addition, one tumour contained ganglioid cells and this was associated with focal immunoreactivity for neurofilament protein, suggesting that some central neurocytomas may, at least focally, continue to differentiate towards the formation of mature neurons.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

中枢神经细胞瘤的特点是位于脑室内,主要发生于年轻人,具有少突胶质细胞瘤样的组织学特征、良性病程以及神经元分化的超微结构证据。我们采用细胞类型特异性免疫细胞化学标记和电子显微镜分析,对11例脑室内中枢神经细胞瘤进行了组织病理学研究。过去,由于中枢神经细胞瘤与其他脑室周围肿瘤具有共同的基本组织病理学特征,这些病变曾引起诊断难题。因此,本系列中的一些肿瘤此前被归类为孟氏孔室管膜瘤或少突胶质细胞瘤。尽管通常被视为良性病变,但本系列中的2例中枢神经细胞瘤显示出间变的组织病理学证据,伴有局灶性坏死、有丝分裂活性和血管增生。所有中枢神经细胞瘤均对神经元特异性烯醇化酶和突触素呈免疫反应,表明存在一致的神经元分化。对3例肿瘤进行了电子显微镜研究,发现其中含有突触小泡、神经突和神经分泌颗粒。此外,1例肿瘤含有神经节样细胞,这与神经丝蛋白的局灶性免疫反应相关,提示一些中枢神经细胞瘤可能至少在局部继续分化为成熟神经元。(摘要截取自250词)

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