Cruz-Pérez Franchesca, Vilá Salvador, Ríos Grissel, Vilá Luis M
Division of Rheumatology, Department of Medicine, University of Puerto Rico Medical Sciences Campus, San Juan, PR, USA.
Case Rep Rheumatol. 2018 Jan 15;2018:1961585. doi: 10.1155/2018/1961585. eCollection 2018.
Macrophage-activating syndrome (MAS) is a rare condition characterized by dysfunctional macrophage activation leading to overproduction of cytokines and phagocytosis of erythrocytes, leukocytes, and platelets. MAS is associated with infectious diseases, malignancies, and autoimmune rheumatic disorders. Herein, we present a 22-year-old Hispanic woman with SLE who was hospitalized because of a three-week history of fever, fatigue, polyarthralgia, nausea, and abdominal pain. Initial laboratories showed severe pancytopenia with marked elevation of liver enzymes and ferritin levels. Bone marrow biopsy revealed macrophages with engulfed erythrocytes consistent with MAS. The patient was treated with high-dose corticosteroids, intravenous immunoglobulins, and cyclosporine 3 mg/kg/day. She had a remarkable clinical response to this therapy. She was continued on cyclosporine, and prednisone dose was gradually decreased to 7.5 mg daily without experiencing recurrent disease. She remained in full clinical remission for 12 months. Our case, together with other reports, suggests that combination therapy with corticosteroids, immunoglobulins, and cyclosporine appears to be effective for patients with SLE-associated MAS. Furthermore, cyclosporine seems to be a good drug for maintenance of remission.
巨噬细胞活化综合征(MAS)是一种罕见病症,其特征为巨噬细胞活化功能异常,导致细胞因子过度产生以及红细胞、白细胞和血小板被吞噬。MAS与感染性疾病、恶性肿瘤和自身免疫性风湿性疾病相关。在此,我们报告一名22岁的西班牙裔系统性红斑狼疮(SLE)女性患者,因持续三周的发热、乏力、多关节痛、恶心和腹痛而住院。初始实验室检查显示严重全血细胞减少,肝酶和铁蛋白水平显著升高。骨髓活检显示巨噬细胞吞噬红细胞,符合MAS表现。该患者接受了大剂量皮质类固醇、静脉注射免疫球蛋白和环孢素3毫克/千克/天的治疗。她对这种治疗有显著的临床反应。继续给予环孢素治疗,泼尼松剂量逐渐减至每日7.5毫克,未出现疾病复发。她完全临床缓解持续了12个月。我们的病例以及其他报告表明,皮质类固醇、免疫球蛋白和环孢素联合治疗对SLE相关的MAS患者似乎有效。此外,环孢素似乎是维持缓解的良好药物。