[An autopsy case of primary progressive multiple sclerosis with minimal acute inflammation and remyelination over an 11-year course].

Q4 Medicine
Clinical Neurology Pub Date : 2025-09-25 Epub Date: 2025-08-28 DOI:10.5692/clinicalneurol.cn-002092
Kohei Asano, Kuniyuki Iwata-Endo, Amane Araki, Saori Morozumi, Yasushi Iwasaki, Keizo Yasui
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引用次数: 0

Abstract

A 32-year-old man presented with the symptoms of a floating sensation, weakness on the right side of the body, and tremor of the right hand. Head MRI was performed, and T2-weighted images showed high-signal lesions around the lateral ventricles, subcortical white matter, and dorsal medulla oblongata. Moreover, MRI of the cervical spine showed multiple high-signal lesions without contrast enhancement. Based on these findings, the patient was diagnosed with primary progressive multiple sclerosis (PPMS) and was treated with steroid pulse therapy, plasma exchange, and oral fingolimod. However, the patient's condition deteriorated slowly, and he died at the age of 43 years. An autopsy revealed multiple demyelinating lesions in the central nervous system. No inflammatory cell infiltration or macrophage accumulation was observed, and there was no evidence of an active lesion. Herein, we present this rare autopsy case of PPMS in Japan with a review of the literature.

[11年的尸检过程中,伴有轻微急性炎症和髓鞘再生的原发性进行性多发性硬化症病例]。
32岁男性,表现为浮感,右侧身体无力,右手震颤。行头部MRI检查,t2加权图像显示侧脑室、皮质下白质和延髓背侧周围有高信号病变。此外,颈椎MRI显示多发高信号病变,未见增强。基于这些发现,患者被诊断为原发性进行性多发性硬化症(PPMS),并接受类固醇脉冲治疗、血浆置换和口服fingolimod。然而,患者病情恶化缓慢,在43岁时去世。尸检显示在中枢神经系统有多发脱髓鞘病变。未见炎症细胞浸润或巨噬细胞积聚,未见活动性病变。在此,我们提出这一罕见的尸检病例的PPMS在日本与文献回顾。
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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来源期刊
Clinical Neurology
Clinical Neurology Medicine-Neurology (clinical)
CiteScore
0.30
自引率
0.00%
发文量
147
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