Padua L, Palmisani M T, Di Trapani G, Evoli A, Larrocca L M, Tonali P
Institute of Neurology, Catholic University, Rome, Italy.
Clin Neuropathol. 1994 Sep-Oct;13(5):292-4.
A 38-year-old man affected with generalized myasthenia gravis (MG) was submitted to thymectomy. At surgery thymic Hodgkin's disease (granulomatous thymoma) and an area of thymic hyperplasia were found. Subsequently, after treatment with anticholinesterase and corticosteroids, the patient achieved clinical remission. The development of MG in this patient could be related to the presence of thymic hyperplasia, rather than to the granulomatous thymoma. Family history revealed that a brother of the patient was affected by non-Hodgkin T-cell lymphoma. Human leukocyte antigens (HLA) were identical in the two affected siblings. The present report suggests a possible link between MG and lymphoproliferative disorders whose mechanism still needs to be clarified.
一名38岁的全身性重症肌无力(MG)男性患者接受了胸腺切除术。手术中发现胸腺霍奇金病(肉芽肿性胸腺瘤)和胸腺增生区域。随后,在接受抗胆碱酯酶和皮质类固醇治疗后,患者实现了临床缓解。该患者MG的发生可能与胸腺增生有关,而非肉芽肿性胸腺瘤。家族史显示,患者的一个兄弟患有非霍奇金T细胞淋巴瘤。两名患病兄弟姐妹的人类白细胞抗原(HLA)相同。本报告提示MG与淋巴增殖性疾病之间可能存在联系,其机制仍有待阐明。