CAJ | 학술논문

胸腺瘤合并重症肌无力(MG)发病机制尚未完全明确,其诊断通过临床表现、影像学及实验室检查并无困难,但治疗方法存在争议且尚无明确治疗原则.多数学者认为,胸腺瘤合并MG患者应首选手术,对于不宜手术者可以考虑放疗及化疗,同时配合抗胆碱酯酶药及类固醇药物治疗.
흉선류합병중증기무력(MG)발병궤제상미완전명학,기진단통과림상표현、영상학급실험실검사병무곤난,단치료방법존재쟁의차상무명학치료원칙.다수학자인위,흉선류합병MG환자응수선수술,대우불의수술자가이고필방료급화료,동시배합항담감지매약급류고순약물치료.
The mechanism of development of thymomas associated with myasthenia gravis(MG) is not completely clear. It is not hard to make diagnosis of thymomas associated with MG via clinical manifestation,radiological investigation and laboratory examination, however, the treatment of thymomas associated with MG remains controversial and there is no straightforward guidelines in the literatures. Most scholars think surgery is the first choice to treat thymomas associated with MG, but for those who are not suitable for surgery, radiotherapy and chemotherapy would be considered to be their choice combined with anti-cholinesterase and steroidsdrugs therapy.