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混合性结缔组织病合并多中心性Castleman病。

Mixed connective tissue disease associated with multicentric Castleman's disease.

作者信息

Nanki T, Tomiyama J, Arai S

机构信息

Department of Internal Medicine, Tokyo Metropolitan Bokuto General Hospital, Japan.

出版信息

Scand J Rheumatol. 1994;23(4):215-7. doi: 10.3109/03009749409103064.

Abstract

We describe a 60-year-old woman who developed mixed connective tissue disease (MCTD) associated with multicentric Castleman's disease (MCD) and Crow-Fukase syndrome (CFS). She showed HLA DR-4 antigen and an abnormal X chromosome (47,XXX). The serum interleukin-6 (IL-6) level was markedly increased and IL-6 mRNA was detected in enlarged lymph node cells. After prednisolone was administered, her IL-6 level decreased and the symptoms of MCTD, MCD, and CFS all improved. Thus, IL-6 may be involved in the modification of the pathologic condition in this patient.

摘要

我们描述了一名60岁女性,她患有一种与多中心Castleman病(MCD)和Crow-Fukase综合征(CFS)相关的混合性结缔组织病(MCTD)。她表现出HLA DR-4抗原和一条异常的X染色体(47,XXX)。血清白细胞介素-6(IL-6)水平显著升高,并且在肿大的淋巴结细胞中检测到IL-6信使核糖核酸。给予泼尼松龙后,她的IL-6水平下降,MCTD、MCD和CFS的症状均有所改善。因此,IL-6可能参与了该患者病理状况的改变。

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