环孢素a治疗多腺体自身免疫综合征

Acta medica Hungarica Pub Date : 1992-01-01
T Császár, A Patakfalvi
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引用次数: 0

摘要

报告1例30岁女性患者的病史。在四年前发生的未知病毒感染后,胰岛素依赖型糖尿病、白癜风、艾迪生病、闭经、甲状腺功能亢进,最后出现了严重的全血细胞减少症伴血小板减少症。根据临床方面和实验室结果,证实为罕见的多腺体自身免疫性综合征(II型)。替代疗法和类固醇应激疗法也被引入,没有任何改善的迹象。由于缺乏治疗效果,由于严重的血小板减少性出血,使用环孢素a治疗,使疾病完全缓解。目前患者随访,无疾病活动迹象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treatment of polyglandular autoimmune syndrome with cyclosporin-A.

The case history of a 30-year-old female patient is reported. Following an unknown viral infection that had occurred four years earlier, insulin-dependent diabetes mellitus vitiligo, Addison's disease, amenorrhoea, hyperthyreosis and, finally, severe pancytopenia with dominant thrombocytopenia developed. On the basis of clinical aspects and laboratory findings, an infrequent polyglandular autoimmune syndrome (type II) was verified. Substituent therapy and steroid stoss therapy also was introduced, without any sign of improvement. For the lack of therapeutic effect and owing to serious thrombocytopenic bleeding, treatment with Cyclosporin-A was indicated, which produced total remission of the illness. Nowadays the patient being on follow-up, has no sign of disease activity.

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