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一例伴有严重贫血的迟发性系统性红斑狼疮病例。

A case of late-onset systemic lupus erythematosus with severe anemia.

作者信息

Matsumoto Moeko, Kaieda Shinjiro, Honda Seiyo, Ida Hiroaki, Hoshino Tomoaki, Fukuda Takaaki

机构信息

Department of Medicine, Kurume University School of Medicine.

出版信息

Kurume Med J. 2013;60(1):25-8. doi: 10.2739/kurumemedj.ms61004. Epub 2013 Aug 7.

Abstract

A 59-year-old woman was referred to our hospital because of severe anemia and leucopenia. Although she developed mild arthralgia without the typical symptoms of systemic lupus erythematosus (SLE), positivity for anti-Sm antibodies led us to a diagnosis of late-onset SLE. Autoimmune hemolytic anemia (AIHA) and suppression of reticulocyte production were considered to have been involved in the etiology of severe anemia. Administration of oral prednisolone (PSL) resulted in a marked improvement of the hematological abnormalities. As late-onset SLE is rare and patients tend to show the typical symptoms less frequently, close attention should be focused on latent symptoms and immunological findings.

摘要

一名59岁女性因严重贫血和白细胞减少症转诊至我院。尽管她出现了轻度关节痛,但无系统性红斑狼疮(SLE)的典型症状,抗Sm抗体阳性使我们诊断为迟发性SLE。自身免疫性溶血性贫血(AIHA)和网织红细胞生成受抑制被认为与严重贫血的病因有关。口服泼尼松龙(PSL)治疗使血液学异常明显改善。由于迟发性SLE罕见,患者出现典型症状的频率较低,因此应密切关注潜在症状和免疫学检查结果。

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