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系统性红斑狼疮中抗胰岛素受体抗体所致的低血糖症。

Hypoglycemia due to antiinsulin receptor antibodies in systemic lupus erythematosus.

作者信息

Varga J, Lopatin M, Boden G

机构信息

Department of Medicine, Jefferson Medical College, Philadelphia, PA 19107-6799.

出版信息

J Rheumatol. 1990 Sep;17(9):1226-9.

PMID:2290167
Abstract

An elderly woman with unexplained episodic fasting hypoglycemia was hospitalized for ascites. Evaluation revealed polyserositis, arthritis and immunologic abnormalities that suggested the diagnosis of systemic lupus erythematosus (SLE). Antibodies to insulin receptor with insulin binding inhibitory activity were detected in her serum. Treatment with prednisone was accompanied by resolution of hypoglycemic episodes and disappearance of the antireceptor antibodies. Autoantibody mediated alterations in serum glucose may be included in the growing list of autoimmune phenomena in SLE. Antiinsulin receptor antibodies should be sought in patients with SLE and idiopathic hypoglycemia.

摘要

一名患有不明原因发作性空腹低血糖的老年女性因腹水住院。评估发现多浆膜炎、关节炎和免疫异常,提示诊断为系统性红斑狼疮(SLE)。在她的血清中检测到具有胰岛素结合抑制活性的胰岛素受体抗体。泼尼松治疗后低血糖发作缓解,抗受体抗体消失。自身抗体介导的血清葡萄糖改变可能是SLE中不断增加的自身免疫现象之一。对于SLE和特发性低血糖患者,应寻找抗胰岛素受体抗体。

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