Pandian J D, Mathuranath P S, Suresh P A, Radhakrishnan K
Department of Neurology, Sree Chitra Tirunal Institute of Medical Sciences and Technology, Trivandrum - 695 011, India.
Neurol India. 1998 Jul-Sep;46(3):232-234.
An adult male with thymomatous myasthenia gravis (MG) and a motor neuron syndrome simulating amyotrophic lateral sclerosis is reported. After thymectomy and corticosteroid therapy, the MG remitted. During 4 years of follow-up, the lower motor neuronsigns in the upper limbs and upper motor neuron signs in the lower limbs remained unchanged. Literature concerning paraneoplastic neurological syndromes associated with thymoma has been reviewed.
报告了一名患有胸腺瘤型重症肌无力(MG)且伴有类似肌萎缩侧索硬化的运动神经元综合征的成年男性。胸腺切除术后及接受皮质类固醇治疗后,重症肌无力缓解。在4年的随访期间,上肢的下运动神经元体征和下肢的上运动神经元体征保持不变。对与胸腺瘤相关的副肿瘤性神经综合征的文献进行了综述。