Herath H M M T B, Pahalagamage S P, Senanayake Sunethra
National Hospital, Colombo, Sri Lanka.
BMC Res Notes. 2018 Mar 14;11(1):177. doi: 10.1186/s13104-018-3287-8.
The pathogenesis of osmotic demyelination syndrome is not completely understood and usually occurs with severe and prolonged hyponatremia, particularly with rapid correction. It can occur even in normonatremic patients, especially who have risk factors like alcoholism, malnutrition and liver disease. Bilateral tongue fasciculations with denervation pattern in electromyogram is a manifestation of damage to the hypoglossal nucleus or hypoglossal nerves. Tongue fasciculations were reported rarely in some cases of osmotic demyelination syndrome, but the exact mechanism is not explained.
A 32-year-old Sri Lankan male, with a history of daily alcohol consumption and binge drinking, presented with progressive difficulty in walking, dysphagia, dysarthria and drooling of saliva and alteration of consciousness. On examination he was akinetic and rigid resembling Parkinsonism with a positive Babinski sign. Clinical features were diagnostic of osmotic demyelination syndrome and MRI showed abnormal signal intensity within the central pons and basal ganglia. He also had tongue fasciculations. The electromyogram showed denervation pattern in the tongue with normal findings in the limbs. Medulla and bilateral hypoglossal nerves were normal in MRI.
We were unable to explain the exact mechanism for the denervation of the tongue, which resulted in fasciculations in this chronic alcoholic patient who developed osmotic demyelination syndrome. The hypoglossal nuclei are located in the dorsal medulla and radiologically undetected myelinolysis of the medulla is a possibility. Hypoglossal nerve damage caused by methanol or other toxic substances that can contaminate regular ethyl alcohol is another possibility, as it is known to cause neurological and radiological features similar to osmotic demyelination syndrome with long-term exposure. So these toxic substances might play a role in chronic alcoholic patients with central pontine myelinolysis.
渗透性脱髓鞘综合征的发病机制尚未完全明确,通常发生于严重且持续时间较长的低钠血症,尤其是快速纠正低钠血症时。甚至在血钠正常的患者中也可能发生,特别是那些有酗酒、营养不良和肝病等危险因素的患者。肌电图显示双侧舌肌束颤并有失神经模式是舌下神经核或舌下神经受损的表现。在一些渗透性脱髓鞘综合征病例中,舌肌束颤的报道很少,但确切机制尚不清楚。
一名32岁的斯里兰卡男性,有每日饮酒和暴饮史,出现进行性行走困难、吞咽困难、构音障碍、流涎及意识改变。检查时,他表现为运动不能和强直,类似帕金森综合征,巴宾斯基征阳性。临床特征诊断为渗透性脱髓鞘综合征,MRI显示脑桥中央和基底节区信号强度异常。他也有舌肌束颤。肌电图显示舌肌有失神经模式,肢体检查结果正常。MRI显示延髓和双侧舌下神经正常。
我们无法解释该慢性酒精中毒患者发生渗透性脱髓鞘综合征时舌肌失神经导致束颤的确切机制。舌下神经核位于延髓背侧,延髓未被影像学检测到的髓鞘溶解是一种可能。甲醇或其他可污染普通乙醇的有毒物质导致舌下神经损伤是另一种可能,因为已知长期接触这些物质会导致类似于渗透性脱髓鞘综合征的神经学和影像学特征。因此,这些有毒物质可能在患有中枢性桥脑髓鞘溶解症的慢性酒精中毒患者中起作用。