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重症肌无力与原发性胆汁性肝硬化。共同的免疫学特征及罕见的巧合。

Myasthenia gravis and primary biliary cirrhosis. Common immunological features and rare coincidence.

作者信息

Kiechl S, Kohlendorfer U, Willeit J, Pohl P, Vogel W

机构信息

Department of Neurology, University Clinic Innsbruck, Austria.

出版信息

Acta Neurol Scand. 1996 Apr;93(4):263-5. doi: 10.1111/j.1600-0404.1996.tb00518.x.

Abstract

A 43-year-old woman with recently diagnosed primary biliary cirrhosis developed antibody-negative myasthenia gravis. She did not receive D-penicillamine therapy. Clinical and immunological features of this patient are discussed. In previous reports on an association between primary biliary cirrhosis and myasthenia D-penicillamine treatment was an obligate causal linkage between both disorders.

摘要

一名最近被诊断为原发性胆汁性肝硬化的43岁女性患了抗体阴性重症肌无力。她未接受青霉胺治疗。本文讨论了该患者的临床和免疫学特征。在先前有关原发性胆汁性肝硬化与重症肌无力之间关联的报告中,青霉胺治疗是这两种疾病之间必然的因果联系。

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