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[一例混合性结缔组织病发展为进行性系统性硬化症、系统性红斑狼疮、多发性肌炎和干燥综合征重叠综合征]

[A case of mixed connective tissue disease developed into overlap syndrome of progressive systemic sclerosis, systemic lupus erythematosus, polymyositis and Sjögren's syndrome].

作者信息

Akiyama Y, Suzuki T, Tanaka M, Kobayashi K, Kagiri T, Ishibashi T, Kitagawa H, Imai F, Hara K, Doi Y

机构信息

Second Department of Internal Medicine, Saitama Medical School.

出版信息

Arerugi. 1990 Jun;39(6):542-7.

PMID:2222196
Abstract

We encountered a patient who developed an overlap syndrome of progressive systemic sclerosis (PSS), systemic lupus erythematosus (SLE), polymyositis (PM) and Sjögren's syndrome (SjS) while we were treating her for mixed connective tissue disease (MCTD). This 42-year-old woman had been photosensitive since 18 years of age. In 1986, Raynaud's phenomenon, swollen hands and arthralgia appeared; therefore, we started to treat this patient based on a diagnosis of MCTD. At that time, her anti-RNP antibody titer was 82,920, but she was negative to anti-Sm antibody. In 1988, she was admitted to our hospital with chief complaints of aggravation of polyarthralgia and myalgia. On physical examination, she showed difficulty in opening her mouth, systemic dermal sclerosis, a decrease in muscular strength and rales. In laboratory tests, her myogenic enzyme level was increased, and she was found to be positive to LE cells, antinuclear antibody, anti-DNA antibody, anti-ENA antibody and anti-SSA antibody. Furthermore, histological features clearly corresponding to those of PSS were found by skin biopsy, myogenic changes by electromyography, evidence of chronic inflammation of the salivary glands by lip biopsy, and proliferative changes in the mesangium were detected by renal biopsy. The concept of MCTD, especially the differences from overlap syndrome, is vague. Therefore we need further study about many cases. Since there have been no reports on cases having sufficient evidence of the development of the overlap syndrome of PSS, SLE, PM and SjS during a course of MCTD, our patient would provide very useful data contributing to the study of MCTD.

摘要

在我们治疗一名混合性结缔组织病(MCTD)患者时,她出现了进行性系统性硬化症(PSS)、系统性红斑狼疮(SLE)、多发性肌炎(PM)和干燥综合征(SjS)的重叠综合征。这位42岁的女性自18岁起就对光敏感。1986年,出现雷诺现象、手部肿胀和关节痛;因此,我们基于MCTD的诊断开始对该患者进行治疗。当时,她的抗RNP抗体滴度为82,920,但抗Sm抗体为阴性。1988年,她因多关节痛和肌痛加重为主诉入院。体格检查时,发现她张口困难、全身性皮肤硬化、肌力下降及啰音。实验室检查中,她的肌源性酶水平升高,并且发现她对LE细胞、抗核抗体、抗DNA抗体、抗ENA抗体和抗SSA抗体呈阳性。此外,皮肤活检发现了与PSS明显相符的组织学特征,肌电图显示有肌源性改变,唇腺活检发现唾液腺慢性炎症的证据,肾活检检测到肾小球系膜的增殖性改变。MCTD的概念,尤其是与重叠综合征的区别,尚不明确。因此我们需要对更多病例进行进一步研究。由于尚无关于在MCTD病程中出现PSS、SLE、PM和SjS重叠综合征充分证据病例的报道,我们的患者将为MCTD的研究提供非常有用的数据。

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