贝里穆马布
医学
狼疮性肾炎
蛋白尿
肾活检
高丙种球蛋白血症
泼尼松龙
内科学
系统性红斑狼疮
胃肠病学
免疫学
托珠单抗
糖皮质激素
皮肤病科
血清学
抗体
活检
疾病
肾
B细胞激活因子
B细胞
作者
Motohisa Yamamoto,Satsuki Aochi,Chisako Suzuki,Seiji Nakamura,Rieko Murakami,Yoshihide Ogawa,Hiroki Takahashi
出处
期刊:Lupus
[SAGE]
日期:2019-03-27
卷期号:28 (6): 786-789
被引量:15
标识
DOI:10.1177/0961203319840430
摘要
Immunoglobulin (Ig)G4-related disease (IgG4-RD) is an unusual complication of systemic lupus erythematosus (SLE). We report a case in which belimumab proved efficacious for not only SLE, but also IgG4-RD. A 58-year-old Japanese woman had suffered from photodermatosis and erythema on the limbs for 20 years. She presented in slight fever and fatigue since 2016. Laboratory data showed hypergammaglobulinemia, proteinuria and positive results for anti-nuclear antibody and anti-double-stranded DNA antibody. Furthermore, elevated levels of serum IgG4 were detected. Contrast-enhanced computed tomography disclosed multiple areas of poor enhancement in the kidneys. The patient was diagnosed with lupus nephritis and IgG4-RD from renal biopsy. Treatment was started with prednisolone at 40 mg/day and mycophenolate mofetil. Proteinuria and serological findings improved initially, but tapering the dose of glucocorticoid proved difficult. After treatment was started with belimumab, clinical symptoms and proteinuria resolved completely. The dose of glucocorticoid was successfully tapered and serum concentration of IgG4 fell further. This appears to represent the first report of a case in which both SLE and IgG4-RD were effectively treated using belimumab.
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