Totsuka S, Hattori T, Yazaki M, Nagao K, Mizushima S
Folia Psychiatr Neurol Jpn. 1985;39(2):155-66. doi: 10.1111/j.1440-1819.1985.tb02899.x.
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.
对9例神经白塞病进行了临床病理研究。中枢神经系统的病理表现如下:好发部位为脑干,其次为脊髓、大脑和小脑。特征性改变为小血管周围反复发生炎症,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,还偶尔出现红细胞渗出、神经细胞和少突胶质细胞变性、胶质结节、髓鞘和轴突破坏、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聚集外,没有病毒颗粒的证据。