A rare trigger for macrophage activation syndrome

被引：22

作者：

Agarwal, Shikhar ^{[2
]}

Moodley, Jayavani ^{[2
]}

Goel, Gati Ajani ^{[2
]}

Theil, Karl S. ^{[3
]}

Mahmood, Syed S. ^{[4
]}

Lang, Richard S. ^{[1
]}

机构：

[1] Cleveland Clin Fdn, Dept Prevent Med, Cleveland, OH 44195 USA

[2] Cleveland Clin Fdn, Dept Internal Med, Cleveland, OH 44195 USA

[3] Cleveland Clin Fdn, Dept Clin Pathol, Cleveland, OH 44195 USA

[4] Case Western Reserve Univ, Sch Med, Cleveland, OH USA

来源：

RHEUMATOLOGY INTERNATIONAL | 2011年 / 31卷 / 03期

关键词：

Macrophage activation syndrome; Histoplasma; Hemophagocytosis;

D O I：

10.1007/s00296-009-1204-0

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Macrophage activation syndrome (MAS) is a disorder characterized by increased activation of mononuclear cells leading to phagocytosis of blood cell precursors in the bone marrow. We describe a case of MAS triggered by disseminated histoplasmosis occurring in a patient with Still's disease on long-term treatment with adalimumab.

引用

页码：405 / 407

页数：3

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