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少关节型幼年特发性关节炎与重症肌无力的关联。

The association of pauciarticular juvenile arthritis and myasthenia gravis.

作者信息

Glass J B, Sher P K, Lennon V A, Regelmann W E

机构信息

Department of Pediatrics, University of Minnesota, Minneapolis.

出版信息

Am J Dis Child. 1991 Oct;145(10):1176-80. doi: 10.1001/archpedi.1991.02160100108033.

Abstract

We encountered two children with fluorescent antinuclear antibody-positive pauciarticular juvenile arthritis who later developed myasthenia gravis. Acetylcholine receptor binding, blocking, and modulating antibodies, retrospectively tested on frozen serum, yielded negative results before the onset of myasthenic symptoms but all yielded strongly positive results coincident with the onset of weakness. In both children, myasthenia gravis responded to thymectomy, and one child had a beneficial response to plasmapheresis. Although, to our knowledge, only two patients with juvenile arthritis and myasthenia gravis have been described in the past, the presence of two additional children with both diseases in a single clinic population suggests that the association may be more prevalent than previously suspected.

摘要

我们遇到了两名荧光抗核抗体阳性的少关节型幼年特发性关节炎患儿,他们后来发展为重症肌无力。对冷冻血清进行回顾性检测,结果显示在肌无力症状出现前,乙酰胆碱受体结合、阻断和调节抗体检测均为阴性,但在肌无力症状出现时所有检测结果均呈强阳性。两名患儿的重症肌无力经胸腺切除术后均有改善,其中一名患儿接受血浆置换治疗后也有良好反应。据我们所知,过去仅有两例幼年特发性关节炎合并重症肌无力的病例报道,而在同一临床群体中又出现了另外两名同时患有这两种疾病的患儿,这表明这种关联可能比之前认为的更为普遍。

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