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2
Application of the 2016 EULAR/ACR/PRINTO Classification Criteria for Macrophage Activation Syndrome in Patients with Adult-onset Still Disease.2016年欧洲抗风湿病联盟/美国风湿病学会/儿童风湿病国际研究组织成人斯蒂尔病患者巨噬细胞活化综合征分类标准的应用
J Rheumatol. 2017 Jul;44(7):996-1003. doi: 10.3899/jrheum.161286. Epub 2017 Apr 15.
3
Macrophage activation syndrome in systemic lupus erythematosus: a multicenter, case-control study in China.系统性红斑狼疮中巨噬细胞活化综合征:中国多中心病例对照研究。
Clin Rheumatol. 2018 Jan;37(1):93-100. doi: 10.1007/s10067-017-3625-6. Epub 2017 Apr 13.
4
In-hospital mortality in febrile lupus patients based on 2016 EULAR/ACR/PRINTO classification criteria for macrophage activation syndrome.基于 2016 年 EULAR/ACR/PRINTO 分类标准的巨噬细胞活化综合征的发热性狼疮患者住院死亡率。
Semin Arthritis Rheum. 2017 Oct;47(2):216-221. doi: 10.1016/j.semarthrit.2017.02.002. Epub 2017 Feb 8.
5
TAC-TIC use of tacrolimus-based regimens in lupus nephritis.TAC-TIC:他克莫司方案在狼疮性肾炎中的应用
Lupus Sci Med. 2016 Dec 29;3(1):e000169. doi: 10.1136/lupus-2016-000169. eCollection 2016.
6
[The clinical characteristics of macrophage activation syndrome secondary to systemic lupus erythematosus].[系统性红斑狼疮继发巨噬细胞活化综合征的临床特征]
Zhonghua Nei Ke Za Zhi. 2016 Nov 1;55(11):840-844. doi: 10.3760/cma.j.issn.0578-1426.2016.11.005.
7
2016 Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis: A European League Against Rheumatism/American College of Rheumatology/Paediatric Rheumatology International Trials Organisation Collaborative Initiative.2016 年巨噬细胞活化综合征合并全身型幼年特发性关节炎分类标准:欧洲抗风湿病联盟/美国风湿病学会/儿科风湿病国际研究组织合作倡议
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环孢素在一名伴有巨噬细胞活化综合征的系统性红斑狼疮患者诱导和维持缓解中的疗效

Efficacy of Cyclosporine in the Induction and Maintenance of Remission in a Systemic Lupus Erythematosus Patient Presenting with Macrophage-Activating Syndrome.

作者信息

Cruz-Pérez Franchesca, Vilá Salvador, Ríos Grissel, Vilá Luis M

机构信息

Division of Rheumatology, Department of Medicine, University of Puerto Rico Medical Sciences Campus, San Juan, PR, USA.

出版信息

Case Rep Rheumatol. 2018 Jan 15;2018:1961585. doi: 10.1155/2018/1961585. eCollection 2018.

DOI:10.1155/2018/1961585
PMID:29552369
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5821990/
Abstract

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.

摘要

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。