Short Cathy L, Scott Grace, Blumbergs Peter C, Koblar Simon A
Department of Neurology, The Queen Elizabeth Hospital, South Australia.
J Clin Neurosci. 2005 Aug;12(6):706-9. doi: 10.1016/j.jocn.2004.08.032.
Motor Neurone Disease (MND) is one of the commonest neurodegenerative disorders of adulthood. MND characteristically presents with a combination of both upper and lower motor neurone features. Primary Lateral Sclerosis (PLS) is thought to be a variant of MND presenting with purely upper motor neurone signs. Debate continues over whether PLS constitutes a distinct pathological entity or whether it is part of the spectrum of motor neurone diseases that present as an upper motor neurone-predominant form of MND. We present a case of MND with purely upper motor neurone features and a prominent pain component. A pre-mortem diagnosis of PLS was made, however autopsy findings demonstrated both upper and lower motor neurone involvement. We believe these findings support the view that PLS is not a discrete pathological entity, but that it is a part of the range of motor neurone diseases that present with predominant but not exclusive upper motor neurone involvement. This case also highlights the feature that pain may be associated with MND even though it is not appreciated to have a sensory pathology.
运动神经元病(MND)是成年期最常见的神经退行性疾病之一。MND的典型表现是上、下运动神经元特征的组合。原发性侧索硬化症(PLS)被认为是MND的一种变体,仅表现为上运动神经元体征。关于PLS是一种独特的病理实体,还是作为以MND的上运动神经元为主型形式出现的运动神经元疾病谱的一部分,仍存在争议。我们报告一例具有纯上运动神经元特征且伴有明显疼痛成分的MND病例。生前诊断为PLS,但尸检结果显示上、下运动神经元均受累。我们认为这些发现支持以下观点:PLS不是一个独立的病理实体,而是以主要但并非仅有的上运动神经元受累为特征的运动神经元疾病范围的一部分。该病例还突出了这样一个特点,即疼痛可能与MND相关,尽管未发现有感觉病理学改变。