Department of Neurology, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.
J Neurol Neurosurg Psychiatry. 2010 Jun;81(6):619-22. doi: 10.1136/jnnp.2008.169243. Epub 2010 Feb 22.
Leucodystrophy with neuroaxonal spheroids (LNS) is rare. There have been fewer than 10 sporadic cases reported, all occurring in the fourth to sixth decades of life. Previously unreported diffusion weighted imaging (DWI) changes on brain imaging in LNS are described as well as the first neurocognitive profile of this disorder in a 24-year-old woman. Neuropsychological testing demonstrated a global cognitive decline, with deficits most representative of a frontal-subcortical dementia. Bright DWI and corresponding dark apparent diffusion coefficient changes were initially mistaken for acute cerebral infarction but then persisted for 19 weeks. Biopsy of a bright DWI lesion showed no evidence of vascular disease and confirmed this rare diagnosis. Given the number of patients with the diagnosis of cerebrovascular disease, supported by DWI findings, we propose other milder cases of LNS may be overlooked.
伴有神经轴突球体的脑白质营养不良(LNS)较为罕见。据报道,散发性病例不到 10 例,均发生在第四至第六个十年。本文描述了 LNS 脑影像学上以前未报道过的弥散加权成像(DWI)改变,并报道了首例 24 岁女性的该疾病的神经认知特征。神经心理学测试显示全面认知能力下降,主要表现为额皮质下痴呆。弥散加权成像上亮信号和相应的表观弥散系数(ADC)低信号改变最初误诊为急性脑梗死,但随后持续了 19 周。亮 DWI 病变的活检未发现血管疾病的证据,从而确诊了这一罕见的诊断。鉴于 DWI 发现支持的脑血管疾病患者数量,我们提出可能会忽视其他较轻的 LNS 病例。