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重症肌无力胸腺切除术与血清乙酰胆碱受体抗体的前瞻性研究

A prospective study of thymectomy and serum acetylcholine receptor antibodies in myasthenia gravis.

作者信息

Olanow C W, Wechsler A S, Roses A D

出版信息

Ann Surg. 1982 Aug;196(2):113-21. doi: 10.1097/00000658-198208000-00001.

Abstract

Forty-seven consecutively presenting myasthenia gravis (MG) patients with generalized weakness were treated according to a standardized prospective protocol. All patients underwent a sternal splitting "total" thymectomy. Medical status before surgery was optimized by plasmapheresis without immunosuppression. Medications were avoided or discontinued whenever possible. All patients were improved. At the time of latest follow-up 83% were free of generalized weakness and 61% were on no medications. There was no significant change in Acetylcholine Receptor Antibody (AChR-AB) titer. The following conclusions were made: (1) thymectomy is an effective therapy for MG, (2) additional medications are not necessary in the majority of patients, and (3) a reduction in the AChR-AB titer is not essential for clinical benefit.

摘要

47例连续就诊的伴有全身无力的重症肌无力(MG)患者按照标准化的前瞻性方案接受治疗。所有患者均接受胸骨劈开“全”胸腺切除术。术前通过血浆置换优化医学状态,不进行免疫抑制。尽可能避免或停用药物。所有患者均有改善。在最近一次随访时,83%的患者无全身无力症状,61%的患者未服用任何药物。乙酰胆碱受体抗体(AChR-AB)滴度无显著变化。得出以下结论:(1)胸腺切除术是治疗MG的有效方法;(2)大多数患者不需要额外用药;(3)AChR-AB滴度降低对临床获益并非必不可少。

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Myasthenia gravis.重症肌无力
Surg Clin North Am. 1980 Aug;60(4):931-45. doi: 10.1016/s0039-6109(16)42192-4.
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Controversies about the treatment of myasthenia gravis.重症肌无力治疗方面的争议。
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The pathogenesis of myasthenia gravis--a hypothesis.重症肌无力的发病机制——一种假说
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