An autopsied case of acute lymphocytic meningoencephalitis with a long clinical course: special reference to CT, MR, SPECT and neuropathological findings.

K Mizukami, Y Tanaka, T Arai, M Sasaki, H Shiraishi, H Horiguchi, Y Nakamura, T Ogata
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Abstract

This report describes the clinico-pathological features of acute lymphocytic meningoencephalitis (ALME) of a patient with a long clinical course of 24 months. The patient rapidly developed a confusional state, occasionally with stupor, various involuntary movements and generalized convulsions followed by fever and headache at the age of 29. Clinical symptoms, except fever and convulsions, had not distinctly improved throughout the clinical course, and cortical atrophy on CT and MR gradually progressed. SPECT revealed a low blood perfusion in the cerebral cortices. Neuropathologically, inflammatory findings were very mild, but nerve cells degenerated prominently. From these clinicopathological findings, it is suggested that chronic degenerative changes followed an acute inflammatory phase.

临床病程较长的急性淋巴细胞性脑膜脑炎1例:特别参考CT、MR、SPECT及神经病理表现。
本报告描述急性淋巴细胞性脑膜脑炎(ALME)患者的临床病理特征,临床病程长达24个月。患者29岁时迅速出现神志不清,偶有麻木、各种不自主运动和全身抽搐,并伴有发热和头痛。临床症状除发热和惊厥外无明显改善,CT和MR显示皮质萎缩逐渐加重。SPECT显示大脑皮质血流灌注低。神经病理学上,炎症表现非常轻微,但神经细胞变性明显。从这些临床病理结果来看,提示慢性退行性改变之后是急性炎症期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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