Motomura S, Tabira T, Kuroiwa Y
J Neurol Neurosurg Psychiatry. 1980 Mar;43(3):210-3. doi: 10.1136/jnnp.43.3.210.
Clinical comparisons were made between Japanese patients with multiple sclerosis (66 cases) and neuro-Behçet's syndrome (23 cases). Those with neuro-Behçet showed marked male predominance, while those with multiple sclerosis showed slight female preponderance. Both showed encephalomyelopathy disseminated in time and space. Patients with multiple sclerosis, however, showed a more polyphasic course, whilst those with neuro-Behçet showed a more progressive one. In multiple sclerosis optic neuritis, acute transverse myelitis, painful tonic seizures, mental disturbance and internuclear ophthalmoplegia were common. On the other hand, in neuro-Behçet the main neurological manifestation was progressive pseudobulbar palsy. Serum and CSF showed more inflammatory changes in neuro-Behçet than in multiple sclerosis. Clinical estimation suggested that in multiple sclerosis the main lesions were in the optic nerve, tegmentum of the brain stem and spinal cord, whereas in neuro-Behçet they were in the basal parts of the brain stem.
对日本的多发性硬化症患者(66例)和神经白塞病患者(23例)进行了临床比较。神经白塞病患者中男性明显居多,而多发性硬化症患者中女性略占优势。两者均表现为时间和空间上播散性的脑脊髓病。然而,多发性硬化症患者的病程多相性更强,而神经白塞病患者的病程进展性更强。在多发性硬化症中,视神经炎、急性横贯性脊髓炎、痛性强直性发作、精神障碍和核间性眼肌麻痹很常见。另一方面,在神经白塞病中,主要的神经学表现是进行性假性延髓麻痹。血清和脑脊液显示,神经白塞病中的炎症变化比多发性硬化症中更多。临床评估表明,在多发性硬化症中,主要病变位于视神经、脑干被盖和脊髓,而在神经白塞病中,病变位于脑干基部。