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首页> 外文期刊>BMC Neurology >Trigeminal isolated sensory neuropathy (TISN) and FOSMN syndrome: despite a dissimilar disease course do they share common pathophysiological mechanisms?
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Trigeminal isolated sensory neuropathy (TISN) and FOSMN syndrome: despite a dissimilar disease course do they share common pathophysiological mechanisms?

机译:三叉神经隔离感觉神经病(TISN)和FOSMN综合征:尽管病程不同,它们是否具有共同的病理生理机制?

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Background Patients presenting with bilateral trigeminal hypoesthesia may go on to have trigeminal isolated sensory neuropathy, a benign, purely trigeminal neuropathy, or facial-onset sensory motor neuronopathy (FOSMN), a malignant life-threatening condition. No diagnostic criteria can yet differentiate the two conditions at their onset. Nor is it clear whether the two diseases are distinct entities or share common pathophysiological mechanisms. Methods Seeking pathophysiological and diagnostic information to distinguish these two conditions at their onset, in this neurophysiological and morphometric study we neurophysiologically assessed function in myelinated and unmyelinated fibres and histologically examined supraorbital nerve biopsy specimens with optic and electron microscopy in 13 consecutive patients with recent onset trigeminal hypoesthesia and pain. Results The disease course distinctly differed in the 13 patients. During a mean 10 year follow-up whereas in eight patients the disease remained relatively stable, in the other five it progressed to possibly life-threatening motor disturbances and extra-trigeminal spread. From two to six years elapsed between the first sensory symptoms and the onset of motor disorders. In patients with trigeminal isolated sensory neuropathy (TISN) and in those with FOSMN neurophysiological and histological examination documented a neuronopathy manifesting with trigeminal nerve damage selectively affecting myelinated fibres, but sparing the Ia-fibre-mediated proprioceptive reflex. Conclusions Although no clinical diagnostic criteria can distinguish the two conditions at onset, neurophysiological and nerve-biopsy findings specify that in both disorders trigeminal nerve damage manifests as a dissociated neuronopathy affecting myelinated and sparing unmyelinated fibres, thus suggesting similar pathophysiological mechanisms.
机译:背景表现为双侧三叉神经感觉减退的患者可能继续患有三叉神经孤立性感觉神经病,良性,纯粹三叉神经病或面部发作感觉运动神经病(FOSMN),恶性威胁生命的疾病。目前尚无诊断标准可以区分这两种情况。还不清楚这两种疾病是不同的实体还是共享共同的病理生理机制。方法寻求病理生理学和诊断信息以区分这两种情况,在这项神经生理学和形态计量学研究中,我们通过神经生理学评估了有髓和无髓纤维的功能,并通过光学和电子显微镜组织学检查了眶上神经活检标本,以连续13例近期发病的三叉神经痛患者感觉不足和疼痛。结果13例患者的病程明显不同。在平均10年的随访期间,其中8例患者的疾病保持相对稳定,而其他5例患者则发展为可能危及生命的运动障碍和三叉神经外扩散。从最初的感觉症状到运动障碍发作之间的时间为两到六年。在三叉神经隔绝性感觉神经病(TISN)和FOSMN的患者中,神经生理学和组织学检查表明存在神经病,表现为三叉神经损伤,选择性影响髓鞘纤维,但保留了Ia纤维介导的本体感受反射。结论尽管尚无临床诊断标准可以区分这两种情况,但神经生理学和神经活检结果表明,在这两种疾病中,三叉神经损伤均表现为一种游离的神经病,影响有髓的和无髓的纤维,因此提示了相似的病理生理机制。

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