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巨噬细胞活化综合征作为风湿性疾病的一种并发症:来自伊朗的报告

Macrophage activation syndrome as a complication of rheumatologic disorders, a report from Iran.

作者信息

Assari R, Sadeghi P, Mirmohammadsadeghi A, Ebadi F, Ziaee V

机构信息

Pediatric Rheumatology Research Group, Rheumatology Research Center, Tehran University of Medical Sciences, Tehran.

出版信息

Reumatismo. 2020 Jan 28;71(4):189-198. doi: 10.4081/reumatismo.2019.1204.

Abstract

The objective was to evaluate the clinical and laboratory manifestations and outcomes of the MAS cases in the context of systemic juvenile idiopathic arthritis (SJIA), systemic lupus erythematosus (SLE), Kawasaki disease, poly-articular juvenile idiopathic arthritis (PJIA). Twenty consecutive patients diagnosed with MAS between 2005 and 2016 entered the study. The cases were divided into two groups: in the first, MAS emerged in the context of a previously diagnosed rheumatologic disease, while in the second, MAS was the first presentation of a rheumatologic disease. In the other classification, the cases were divided into recurrent and non-recurrent cases. Laboratory data were recorded at three times: before MAS attack, during MAS attack, and 1 month after discharge from hospital. Nineteen cases with the median age of 5.9 (3.6-10) years entered the study. Four cases (21.1%) showed recurrent attacks of MAS. MAS was the first presentation of disease in 10 cases. The median age of the patients in the underlying disease group (10 years) was significantly higher than in the first presentation group [4.5(1.7-6.1) years, p=0.003]. The median fibrinogen value during MAS attack in the underlying disease group (601 mg/ dL) was also significantly higher than in the first presentation group (174 mg/dL, p=0.038). The platelet count during MAS attack in the recurrent group (30,500/microliter) was significantly lower than in the non-recurrent group (135,000/microliter, p=0.042). Our series of MAS cases demonstrated an overview of the symptoms, signs, laboratory manifestations, treatment, and prognosis of these cases. The higher median fibrinogen in MAS in the underlying disease group revealed that a decreasing level of fibrinogen in chronic disease is more significant than a single cut off value. Indeed, the lower platelet count in the recurrent MAS group may indicate greater platelet consumption due to organomegaly. Early diagnosis and treatment may save the patients' lives.

摘要

目的是评估巨噬细胞活化综合征(MAS)病例在系统性幼年特发性关节炎(SJIA)、系统性红斑狼疮(SLE)、川崎病、多关节型幼年特发性关节炎(PJIA)背景下的临床和实验室表现及转归。2005年至2016年间连续20例诊断为MAS的患者纳入研究。病例分为两组:第一组,MAS出现在先前诊断的风湿性疾病背景下;第二组,MAS是风湿性疾病的首次表现。在另一种分类中,病例分为复发和非复发病例。实验室数据在三个时间点记录:MAS发作前、MAS发作期间以及出院后1个月。19例患者进入研究,中位年龄为5.9(3.6 - 10)岁。4例(21.1%)出现MAS复发。10例中MAS是疾病的首次表现。基础疾病组患者的中位年龄(10岁)显著高于首次表现组[4.5(1.7 - 6.1)岁,p = 0.003]。基础疾病组MAS发作期间的中位纤维蛋白原值(601 mg/dL)也显著高于首次表现组(174 mg/dL,p = 0.038)。复发组MAS发作期间的血小板计数(每微升30,500)显著低于非复发组(每微升135,000,p = 0.042)。我们的一系列MAS病例展示了这些病例的症状、体征、实验室表现、治疗及预后情况。基础疾病组MAS中较高的中位纤维蛋白原表明,慢性病中纤维蛋白原水平的降低比单一临界值更具意义。确实,复发MAS组中较低的血小板计数可能表明由于器官肿大导致血小板消耗更多。早期诊断和治疗可能挽救患者生命。

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