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胚胎发育不良性神经上皮肿瘤(DNT):一项免疫组织化学和超微结构研究。

Dysembryoplastic neuroeptihelial tumor (DNT): an immunohistochemical and ultrastructural study.

作者信息

Hirose T, Scheithauer B W, Lopes M B, VandenBerg S R

机构信息

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota 55905.

出版信息

J Neuropathol Exp Neurol. 1994 Mar;53(2):184-95. doi: 10.1097/00005072-199403000-00010.

DOI:10.1097/00005072-199403000-00010
PMID:8120540
Abstract

To assess the range of differentiation of the cells comprising dysembryoplastic neuroepithelial tumor (DNT), particularly the oligodendrocyte-like cells (OLC), 14 DNT were immunochemically studied with a spectrum of neuronal and glial markers. Eight tumors were also studied ultrastructurally. Neurofilament protein, class III beta-tubulin, and synaptophysin preparations stained a few OLC in two, six and one lesion, respectively. In addition, many OLC within a single cortical nodule were reactive for class III beta-tubulin. The vast majority of OLC were strongly S-100 protein positive. Glial fibrillary acidic protein labeled a fair number of OLC in two cases and one nodule consisted almost entirely of immunoreactive astrocytes. Ultrastructurally, many OLC resembled oligodendrocytes in exhibiting microtubules, prominent Golgi and short cell processes; pericellular lamination of cell processes, a characteristic of oligodendroglia, was noted in only one tumor. In two cases, OLC with astrocytic features were seen to contain small numbers of intermediate filaments. In four cases, a few OLC resembled immature neurons with scant dense-core granules or synapses. This study confirms the glioneuronal nature of DNT, a lesion composed of heterogeneous cells, many resembling oligodendrocytes and a few showing early astrocytic and neuronal differentiation. Although their relation to OLC is unclear, the presence and peculiar distribution of mature neurons is nonetheless an integral diagnostic feature of the lesion.

摘要

为评估构成胚胎发育不良性神经上皮肿瘤(DNT)的细胞,尤其是少突胶质细胞样细胞(OLC)的分化范围,我们用一系列神经元和神经胶质标志物对14例DNT进行了免疫化学研究。对其中8例肿瘤还进行了超微结构研究。神经丝蛋白、Ⅲ类β微管蛋白和突触素制剂分别在2个、6个和1个病灶中使少数OLC染色。此外,单个皮质结节内的许多OLC对Ⅲ类β微管蛋白呈反应性。绝大多数OLC对S-100蛋白呈强阳性。胶质纤维酸性蛋白在2例中标记了相当数量的OLC,1个结节几乎完全由免疫反应性星形胶质细胞组成。超微结构上,许多OLC在显示微管、显著的高尔基体和短细胞突起方面类似于少突胶质细胞;仅在1例肿瘤中观察到细胞突起的细胞周围分层,这是少突胶质细胞的一个特征。在2例中,具有星形胶质细胞特征的OLC可见含有少量中间丝。在4例中,少数OLC类似于未成熟神经元,具有少量致密核心颗粒或突触。本研究证实了DNT的神经胶质神经元性质,该病变由异质性细胞组成,许多类似于少突胶质细胞,少数显示早期星形胶质细胞和神经元分化。尽管它们与OLC的关系尚不清楚,但成熟神经元的存在及其特殊分布仍然是该病变不可或缺的诊断特征。

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