Nawata Takashi, Kubo Makoto, Shiragami Kosaku, Nakamura Yukinori, Yano Masafumi
Department of Medicine and Clinical Science, Division of Cardiology and Clinical Immunology, Yamaguchi University Graduate School of Medicine, Ube, Japan.
Division of Endocrinology, Metabolism, Hematological Science and Therapeutics, Yamaguchi University Graduate School of Medicine, Ube, Japan.
Case Rep Rheumatol. 2017;2017:4159727. doi: 10.1155/2017/4159727. Epub 2017 Sep 14.
An estimated 0.9% to 2.4% of patients with systemic lupus erythematosus (SLE) also have hemophagocytic lymphohistiocytosis (HLH). HLH associated with autoimmune diseases is often refractory to corticosteroid treatment; thus, additional immunosuppressive drugs, such as cyclosporine, cyclophosphamide, or tacrolimus, are required. Here, we describe the case of a 44-year-old Japanese woman who developed HLH associated with lupus nephritis. Initially, her HLH was refractory to treatment with a corticosteroid, tacrolimus, and mizoribine. However, alternative treatment with a corticosteroid, mycophenolate mofetil, and tacrolimus improved both her HLH and lupus nephritis. This case suggests the possibility of mycophenolate mofetil as a key drug for treating HLH associated with SLE.
据估计,系统性红斑狼疮(SLE)患者中有0.9%至2.4%也患有噬血细胞性淋巴组织细胞增生症(HLH)。与自身免疫性疾病相关的HLH通常对皮质类固醇治疗无效;因此,需要使用其他免疫抑制药物,如环孢素、环磷酰胺或他克莫司。在此,我们描述了一名44岁日本女性的病例,她患上了与狼疮性肾炎相关的HLH。最初,她的HLH对皮质类固醇、他克莫司和咪唑立宾治疗无效。然而,使用皮质类固醇、霉酚酸酯和他克莫司的替代治疗改善了她的HLH和狼疮性肾炎。该病例提示霉酚酸酯有可能成为治疗与SLE相关的HLH的关键药物。