Guenther Angela D, Munoz David G
Clin Neuropathol. 2013 Nov-Dec;32(6):486-91. doi: 10.5414/NP300634.
AIMS/BACKGROUND: The pattern of demyelination in the scant autopsy literature on acute disseminated encephalomyelitis (ADEM) is described as perivenous sleeves. We report an unusual neuropathological presentation of ADEM, also known as postinfectious or perivenous encephalomyelitis.
A 19-yearold female patient presented with headache and myalgias, followed by subacute onset of lethargy, confusion, left hemiparesis and dysphasia after an interval of 4 - 5 days. On MRI, extensive subcortical white matter lesions were seen and a diagnosis of ADEM was made after other causes were excluded. The patient received intravenous methylprednisolone and plasma exchange. Neurological symptoms remained stable over the length of the hospital stay (1 month). The patient passed away due to non-neurologic causes.
On autopsy, the brain showed extensive, confluent, plaque-like demyelinating lesions with a striking selectivity for the subcortical white matter sparing the U-fibers. No lesions were discernible in the cortex, the deep grey matter, the cerebellum, the spinal cord or the optic nerves on LFB-stained sections. Only one lesion extended to the periventricular area in the right occipital lobe. Some lesions had a scalloped border and foci of inhomogeneous demyelination, suggestion coalescence of smaller lesions. Histologically, all lesions were of the same age, coupling near complete demyelination with relative preservation of axons, along with scant perivascular lymphohistiocytic cuffing, dense infiltration by foamy macrophages, and prominent gliosis.
The morphology of individual demyelinating< lesions is indistinguishable from the lesions in a new onset case of multiple sclerosis (MS) and adds to the autopsy literature on overlapping neuropathological findings in ADEM and multiple sclerosis.
目的/背景:在关于急性播散性脑脊髓炎(ADEM)的少量尸检文献中,脱髓鞘模式被描述为静脉周围套袖样。我们报告了一例ADEM不寻常的神经病理学表现,ADEM也称为感染后或静脉周围脑脊髓炎。
一名19岁女性患者出现头痛和肌痛,4 - 5天后间隔出现亚急性嗜睡、意识模糊、左侧偏瘫和言语困难。MRI显示广泛的皮质下白质病变,排除其他病因后诊断为ADEM。患者接受了静脉注射甲基泼尼松龙和血浆置换。在住院期间(1个月)神经症状保持稳定。患者因非神经系统原因死亡。
尸检时,大脑显示广泛、融合的斑块样脱髓鞘病变,对皮质下白质有显著选择性,U形纤维未受累。在LFB染色切片上,皮质、深部灰质、小脑、脊髓或视神经未见病变。仅一个病变延伸至右枕叶脑室周围区域。一些病变有扇贝样边界和不均匀脱髓鞘灶,提示较小病变融合。组织学上,所有病变年龄相同,几乎完全脱髓鞘伴轴突相对保留,伴有少量血管周围淋巴细胞组织细胞套袖形成、泡沫巨噬细胞密集浸润和显著胶质增生。
单个脱髓鞘病变的形态与新发多发性硬化(MS)病例中的病变无法区分,这增加了关于ADEM和多发性硬化重叠神经病理学发现的尸检文献。