Clinicopathologic studies on neuro-Behçet's disease.

S Totsuka, T Hattori, M Yazaki, K Nagao, S Mizushima
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引用次数: 20

Abstract

Nine cases of neuro-Behcet's disease were investigated clinicopathologically. Pathological pictures of the central nervous system were characterized as follows: the site of predilection was the brain stem, followed by the spinal cord, cerebrum and cerebellum. The pathognomonic changes were recurrent inflammations around small vessels, causing a softening of the tissue. Lesions were composed of a perivascular infiltration of lymphocytes, histiocytes and microglias and, moreover, diapedesis, degenerated nerve cells and oligodendroglias, glial nodule, breakdown of myelin and axon, fatty granule cells and glio-mesenchymal proliferation were present occasionally. Electron microscopic studies on the neurons revealed no evidence of viral particles except for some accumulations of electron dense bodies.

神经behaperet病的临床病理研究。
对9例神经白塞病进行临床病理分析。中枢神经系统病理表现为:发病部位以脑干为主,其次为脊髓、大脑、小脑。典型的变化是小血管周围的复发性炎症,导致组织软化。病变由淋巴细胞、组织细胞和小胶质细胞的血管周围浸润组成,此外,偶尔还存在渗出、神经细胞和少突胶质细胞变性、胶质结节、髓鞘和轴突破裂、脂肪颗粒细胞和胶质间充质增生。对神经元的电子显微镜研究显示,除了一些电子致密体的积聚外,没有病毒颗粒的证据。
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