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免疫功能低下患者的2例脑炎病例

[2 cases of encephalitis in immunodepressed patients].

作者信息

Bonnaud E, Vital C

出版信息

Ann Anat Pathol (Paris). 1977;22(2):177-92.

PMID:596687
Abstract

The authors report two new cases of encephalitis occurring in association with immunity deficiency. The first concerns a child suffering from Bruton type congenital hypogammaglobulinemia. Histological examination of the brain under light microscopy shows important lesions of panencephalitis with parenchymal atrophy : the latter was more marked in the cerebellar lamellae. Ultra-structural examination showed numerous nuclear bodies in the nuclei of the macroglial cells and tubular inclusions situated in the cytoplasm of the capillary endothelial cells. The second case is that of a man of 44 years of age who had undergone a kidney transplant for malignant arterial hypertension, who after 3 months immunodepressive treatment suffered from temporo-spatial confusion together with a pyramidal tract syndrome. He died after 3 weeks evolution of the disease. Microscopical examination of the encephalon showed the presence of microglial nodules with aspects of neurophagia, suggestive of a polioencephalitis. These lesions were situated in the temporal cortex and the brain stem. The lymphocytic reaction was very slight in the second case.

摘要

作者报告了两例与免疫缺陷相关的脑炎新病例。第一例涉及一名患有布鲁顿型先天性低丙种球蛋白血症的儿童。大脑组织的光学显微镜检查显示全脑炎伴有实质萎缩的重要病变:后者在小脑叶片中更为明显。超微结构检查显示大胶质细胞核中有许多核体,以及位于毛细血管内皮细胞质中的管状包涵体。第二例是一名44岁的男子,因恶性动脉高血压接受了肾脏移植,在免疫抑制治疗3个月后出现颞叶空间定向障碍并伴有锥体束综合征。疾病进展3周后死亡。对脑的显微镜检查显示存在具有噬神经现象的小胶质结节,提示为脑灰质炎。这些病变位于颞叶皮质和脑干。在第二例中淋巴细胞反应非常轻微。

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