Scialò Carlo, Morbelli Silvia, Girtler Nicola, Mandich Paola, Mancardi Giovanni Luigi, Caponnetto Claudia, Nobili Flavio
a Department of Neurosciences , Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI) , Genova , Italy.
b Nuclear Medicine Department of Health Sciences (DISSAL) , University of Genova, IRCCS AOU San Martino-IST , Genova , Italy.
Amyotroph Lateral Scler Frontotemporal Degener. 2015;16(5-6):414-7. doi: 10.3109/21678421.2015.1026828. Epub 2015 May 12.
Mills syndrome is a rare condition characterized by slowly progressive upper motor neuron-predominant hemiparesis, belonging to the motor neuron disorder spectrum. Predominantly unilateral primary degeneration of corticospinal pathways is the supposed underlying pathophysiological mechanism. By means of (18)F-Fluorodeoxyglucose Positron Emission Tomography, we found significant (Statistical Parametric Mapping, SPM, analysis versus controls, uncorrected p < 0.005 at voxel level, p < 0.05 at cluster level, corrected for multiple comparisons) hypometabolism in motor and premotor areas of both hemispheres, mainly contralateral to the limbs weakness in a patient with a 10-year history of slowly progressive left-sided hemiparesis. No significant grey matter loss was found on voxel based morphometry (SPM). This supports the hypothesis of a slowly progressive neurodegenerative process involving primary motor and premotor cortex.
米尔斯综合征是一种罕见疾病,其特征为缓慢进展的以上运动神经元为主的偏瘫,属于运动神经元疾病谱。推测其潜在的病理生理机制是皮质脊髓束主要为单侧原发性变性。通过(18)F-氟脱氧葡萄糖正电子发射断层扫描,我们发现一名有10年缓慢进展性左侧偏瘫病史的患者,其双侧半球的运动和运动前区存在显著(统计参数映射,SPM,与对照组分析,体素水平未校正p<0.005,簇水平p<0.05,经多重比较校正)代谢减低,主要在与肢体无力对侧。基于体素的形态测量学(SPM)未发现明显的灰质丢失。这支持了涉及原发性运动和运动前皮质的缓慢进展性神经退行性过程的假说。