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一名患有威尔逊氏病的患者出现系统性红斑狼疮、甲状旁腺功能减退和溶血性贫血。

Systemic lupus erythematosus, hypoparathyroidism, and hemolytic anemia in a patient with Wilson's disease.

作者信息

Mageed Sarah Abdel, Rawla Prashanth, Mahmoud Mariam Abdelmageed, Shahba Abeer

机构信息

Department of Internal Medicine, Faculty of Medicine, Tanta University, Egypt.

Department of Internal Medicine, SOVAH Health, Martinsville, Virginia, United States.

出版信息

Reumatologia. 2019;57(4):239-242. doi: 10.5114/reum.2019.87622. Epub 2019 Aug 31.

Abstract

The authors report a female case of systemic lupus erythematosus (SLE) that was diagnosed as Wilson's disease (WD) when neurological manifestations were evident three years after the first admission. The brain imaging studies showed bilateral symmetrical basal ganglia involvement, slit lamp examination revealed Kayser-Fleischer ring of the cornea, and 24-hour urinary copper and serum ceruloplasmin also confirmed the diagnosis. The patient also had hemolytic anemia and hypoparathyroidism, which are rare presenting features of WD. SLE may be associated with WD, and presence of neurological, behavioral, or liver function abnormalities should raise the suspicion, even without apparent features of WD.

摘要

作者报告了一例女性系统性红斑狼疮(SLE)病例,该患者在首次入院三年后出现明显神经症状时被诊断为威尔逊病(WD)。脑部影像学检查显示双侧基底节对称性受累,裂隙灯检查发现角膜凯-弗环,24小时尿铜及血清铜蓝蛋白检查也确诊了该病。该患者还患有溶血性贫血和甲状旁腺功能减退,这些都是WD罕见的表现特征。SLE可能与WD相关,即使没有明显的WD特征,出现神经、行为或肝功能异常也应引起怀疑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af1d/6753600/b65aeb0a6296/RU-57-87622-g001.jpg

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