Samejima Shoko, Tateishi Takahisa, Arahata Hajime, Shigeto Hiroshi, Ohyagi Yasumasa, Kira Jun-ichi
Department of Neurology, Neurological Institute, Graduate School of Medical Sciences, Kyushu University.
Rinsho Shinkeigaku. 2010 Jul;50(7):467-72. doi: 10.5692/clinicalneurol.50.467.
We report a case of paraneoplastic neurological syndrome with anti-neuronal antibodies, namely anti-Hu and anti-GluR epsilon 2 antibodies in sera. A 72-year-old male had a transient history of eye movement disorder and sensory neuropathy, which improved spontaneously. Two years later, he was admitted to another hospital because of gait disturbance, numbness of the hands and an attack of unconsciousness with generalized convulsion. He was admitted to our hospital with prolonged consciousness disturbance and muscular weakness of all extremities. On admission his consciousness deteriorated slightly without neck stiffness. His cranial nervous system was normal except for incomplete abduction and elevation of both eyes. The patient had severe distal dominant weakness and atrophy in the muscles of all four limbs. Muscle tonus was decreased and hyporeflexia was noted in the four extremities. Plantar response was extensor. Neither sensory disturbance nor ataxia was observed. Cranial MRI showed T2-weighted high intensity lesions in the bilateral mesial temporal lobes, including the hippocampi. A nerve conduction study revealed motor-dominant peripheral neuropathy with prolonged latency; the amplitudes of compound muscle action potentials were severely reduced in all four limbs and those of sensory nerve action potentials were moderately reduced in the right upper and lower extremities. We also found a left hilar lymphadenopathy showing accumulation of FDG on PET, suggesting a possibility of malignancy. Anti-Hu and anti-GluR epsilon 2 antibodies were detected in sera but not in CSF. We diagnosed him with limbic encephalitis and peripheral neuropathy due to paraneoplastic neurological syndrome and treated him with two courses of intravenous immunoglobulin (IVIg) (400 mg/kg, 5 days). The consciousness disturbance, and prolonged distal latency revealed by motor nerve conduction studies improved slightly. Although the roles of anti-neuronal antibodies in paraneoplastic conditions remain unknown, we consider that IVIg may be worth using to treat cases with anti-Hu and anti-GluR epsilon 2 antibodies.
我们报告一例伴有抗神经元抗体(即血清中的抗Hu和抗GluR ε2抗体)的副肿瘤性神经系统综合征病例。一名72岁男性有短暂的眼球运动障碍和感觉神经病变病史,症状自发改善。两年后,他因步态障碍、手部麻木以及一次伴有全身抽搐的意识丧失发作而入住另一家医院。他因意识障碍延长和四肢肌肉无力入住我院。入院时,他的意识稍有恶化,但无颈部强直。除双眼外展和上抬不完全外,其颅神经系统正常。患者四肢肌肉严重的远端优势性无力和萎缩。肌肉张力降低,四肢反射减弱。巴宾斯基征阳性。未观察到感觉障碍和共济失调。头颅MRI显示双侧内侧颞叶包括海马区T2加权高信号病变。神经传导研究显示运动优势性周围神经病变,潜伏期延长;所有四肢复合肌肉动作电位的波幅严重降低,右上肢和下肢感觉神经动作电位的波幅中度降低。我们还发现左肺门淋巴结肿大,PET显示有FDG聚集,提示有恶性肿瘤的可能。血清中检测到抗Hu和抗GluR ε2抗体,但脑脊液中未检测到。我们诊断他为副肿瘤性神经系统综合征所致的边缘叶脑炎和周围神经病变,并用两个疗程的静脉注射免疫球蛋白(IVIg)(400mg/kg,5天)进行治疗。意识障碍以及运动神经传导研究显示的远端潜伏期延长稍有改善。尽管抗神经元抗体在副肿瘤性疾病中的作用尚不清楚,但我们认为IVIg可能值得用于治疗伴有抗Hu和抗GluR ε2抗体的病例。