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作 者:高波廷[1] 杨明山[1] 徐金技 潘铁成[1] 陈启福[1]
机构地区:[1]同济医科大学同济医院神经科,同济医科大学同济医院心胸外科
出 处:《中国神经精神疾病杂志》1995年第3期141-143,共3页Chinese Journal of Nervous and Mental Diseases
摘 要:69例重症肌无力(MG)病人行胸腺切除术,术前血清乙酰胆碱受体抗体水平均高于正常,术后半年抗体水平明显下降,胸腺增生组(20例)尤为显著.胸腺瘤组(49例)术前胸腺瘤相关抗体水平增高,但术后半年内无明显变化.69例MG患者胸腺切除术后4年,症状总缓解率为76.81%,其中胸腺增生组95%,胸腺瘤组69.39%。作者认为,对于伴有胸腺增生或胸腺瘤的MG患者,胸腺切除术是有效的,应该列为治疗的第一选择。Sixty-nine patients with myasthenia gravis(MG) were divided into 2 groups, thywic hyperplasia and thymoma groups, according to the pathological findingS of thymus. All the patients were. followed up for 4 years after thymectomy, whose sera were detected for acetylcholine receptor antibody(AchRab) and thymoma-associated antibody (CAEab) at regular intervals. The resultS showed that AchRab titers significantly declined in 69 MG patients, particularly in 20 patients With thymic hyperplasia, half a year after thymectomy, but without any change in CAEab. At endpoint, the cumulative remission rate of 69 MG patients underwent thymectomy was 76.81%, with 95% in thymic hyperplasia group, and 69.39% in thymoma one. It is concluded that thymectomy should be a primary therapy in MG patients with thwic hyperplasia or thylnoma.
分 类 号:R746.105[医药卫生—神经病学与精神病学]
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