Department of Neurology, Liuzhou People's Hospital, Liuzhou, China.
Department of Neurology, The First Affiliated Hospital of Shenzhen University, 3002 Sungang West Road, Futian District, Shenzhen City, 518000, China.
BMC Neurol. 2021 Apr 10;21(1):156. doi: 10.1186/s12883-021-02182-z.
Colony-stimulating factor 1 receptor (CSF1R)-related leukoencephalopathy is a rare and rapidly progressive leukoencephalopathy characterized by cognitive, motor, and neuropsychiatric symptoms, which is often misdiagnosed. Magnetic resonance imaging (MRI) signs and follow-up MRI of CSF1R-related leukoencephalopathy could help in establishing a diagnosis, but these features are not widely known by general neurologists.
A 34-year-old man was admitted for progressive weakness of the right limbs over 8 months. His father and sister had a similar clinical evolution. The primary neurological signs were hemiplegia, cognitive decline, dysarthria, pyramidal signs, ataxia and parkinsonism, and rapid disease progression. Cerebrospinal fluid analysis results were normal. Despite receiving treatment for improving cerebral metabolism and relieving the muscle spasm, his symptoms did not improve significantly. Brain MRI showed lesions concentrated in the corpus callosum and the deep white matter of the bilateral parieto-occipital lobes, periventricular areas, and corticospinal tracts. There was an enhanced lesion after a gadolinium-enhanced MRI scan. Over the 8-month progression, the lesions always exhibited restricted diffusion. The diffuse lesions gradually increased as the disease progressed. Genetic sequencing results showed a novel heterozygous missense mutation (c.2267 T > C p.L756P) in the CSF1R gene. The patient was treated with citicoline and idebenone for 4 days to improve cerebral metabolism, but his symptoms did not improve significantly.
The multiple lesions involving the pyramidal tract and white matter showed continuously restricted diffusion on brain imaging and gradually increased with disease progression.
集落刺激因子 1 受体(CSF1R)相关脑白质病是一种罕见的、快速进展性脑白质病,其特征为认知、运动和神经精神症状,常被误诊。磁共振成像(MRI)表现及 CSF1R 相关脑白质病的随访 MRI 有助于诊断,但这些特征并不为普通神经科医生所熟知。
一名 34 岁男性因右侧肢体进行性无力 8 个月就诊。其父亲和姐姐有类似的临床演变。主要的神经体征为偏瘫、认知能力下降、构音障碍、锥体束征、共济失调和帕金森病,且疾病进展迅速。脑脊液分析结果正常。尽管接受了改善脑代谢和缓解肌肉痉挛的治疗,但他的症状没有明显改善。脑部 MRI 显示病变集中在胼胝体和双侧顶枕叶深部白质、脑室周围区和皮质脊髓束。增强 MRI 扫描后出现增强病变。在 8 个月的进展过程中,病变始终表现为弥散受限。随着疾病的进展,弥散性病变逐渐增加。基因测序结果显示 CSF1R 基因存在新的杂合错义突变(c.2267T>C p.L756P)。患者接受胞磷胆碱和艾地苯醌治疗 4 天以改善脑代谢,但症状无明显改善。
涉及锥体束和白质的多发性病变在脑部成像上表现为弥散受限,且随着疾病的进展逐渐增加。