...
首页> 外文期刊>Neuropathology: official journal of the Japanese Society of Neuropathology >Cryptococcal meningitis accompanying lymphocytic inflammation predominantly in cerebral deep white matter: A possible manifestation of immune reconstitution inflammatory syndrome
【24h】

Cryptococcal meningitis accompanying lymphocytic inflammation predominantly in cerebral deep white matter: A possible manifestation of immune reconstitution inflammatory syndrome

机译:隐球菌性脑膜炎伴发淋巴细胞炎症,主要存在于脑深部白质中:免疫重建炎症综合征的可能表现

获取原文
获取原文并翻译 | 示例

摘要

Cryptococcal meningitis is rarely complicated by immune-mediated leukoencephalopathy, but the precise pathomechanism is uncertain. A 72-year-old Japanese man treated with prednisolone for Sweet disease developed a subacute progression of meningitis, which was considered as neuro-Sweet disease. A treatment by methylprednisolone rapidly improved CSF findings with a remarkable decrease in lymphocyte numbers in the blood, but the patient's consciousness still worsened after the cessation of the treatment. The patient developed cryptococcal meningitis and MRI showed abnormal intensities predominantly in the cerebral deep white matter along with the recovery of lymphocyte numbers in the blood, which resulted in death. A postmortem examination of the brain revealed degenerative lesions, especially at the cerebral white matter and cortex adjacent to the leptomeninges abundantly infiltrated by Cryptococcus neoformans. In the affected cerebral deep white matter, perivascular infiltration of lymphocytes was prominent in coexistence with reactive astrocytes and vascular proliferation, but these findings were not observed in the subcortical and cortical lesions. Cryptococcus neoformans was not present within the brain parenchyma. This is the first report of a case suggesting that cryptococcal meningitis can accompany lymphocytic inflammation predominantly in cerebral deep white matter as a possible manifestation of immune reconstitution inflammatory syndrome.
机译:隐球菌性脑膜炎很少并发免疫介导的白质脑病,但确切的发病机制尚不确定。一名接受泼尼松龙治疗甜食病的72岁日本男子出现了脑膜炎的亚急性进展,该病被认为是神经性甜病。甲基泼尼松龙的治疗可以迅速改善CSF的发现,并显着减少血液中的淋巴细胞数量,但是停止治疗后患者的意识仍然恶化。该患者发展为隐球菌性脑膜炎,MRI显示主要是脑深部白质强度异常,同时血液中淋巴细胞数量恢复,从而导致死亡。大脑的事后检查显示有退行性病变,尤其是在大脑白质和与新隐球菌大量浸润的软脑膜相邻的皮质。在受影响的脑深部白质中,淋巴细胞与反应性星形胶质细胞和血管增生并存时,血管周围的淋巴细胞浸润突出,但在皮下和皮层病变中未观察到这些发现。脑实质内不存在新隐球菌。这是一例首次报道隐球菌性脑膜炎可伴发淋巴细胞性炎症,主要发生在脑深部白质中,是免疫重建炎症综合症的一种可能表现。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号