Literature DB >> 17762614

Recognition and management of macrophage activation syndrome in juvenile arthritis.

Alison Kelly1, Athimalaipet V Ramanan.   

Abstract

PURPOSE OF REVIEW: Macrophage activation syndrome is a life-threatening complication seen predominantly in children with systemic onset juvenile idiopathic arthritis. It accounts for a significant amount of the morbidity and mortality seen with systemic onset juvenile idiopathic arthritis. RECENT
FINDINGS: In this article, we will look at the new developments in the diagnosis, classification, pathogenesis and management of macrophage activation syndrome in systemic onset juvenile idiopathic arthritis patients.
SUMMARY: More work is needed to further elucidate the pathophysiology of macrophage activation syndrome in systemic onset juvenile idiopathic arthritis. This would be the key to early diagnosis using more sensitive criteria and better management.

Entities:  

Mesh:

Year:  2007        PMID: 17762614     DOI: 10.1097/BOR.0b013e32825a6a79

Source DB:  PubMed          Journal:  Curr Opin Rheumatol        ISSN: 1040-8711            Impact factor:   5.006


  17 in total

1.  Serum neopterin levels as a diagnostic marker of hemophagocytic lymphohistiocytosis syndrome.

Authors:  Maria F Ibarra; Marisa Klein-Gitelman; Elaine Morgan; Maria Proytcheva; Christine Sullivan; Gabrielle Morgan; Lauren M Pachman; Maurice R G O'Gorman
Journal:  Clin Vaccine Immunol       Date:  2011-01-26

2.  Hypocomplementemia associated with macrophage activation syndrome in systemic juvenile idiopathic arthritis and adult onset still's disease: 3 cases.

Authors:  Mark Gorelik; Kathryn S Torok; Daniel A Kietz; Raphael Hirsch
Journal:  J Rheumatol       Date:  2011-02       Impact factor: 4.666

Review 3.  Macrophage activation syndrome in juvenile dermatomyositis: a systematic review.

Authors:  Dimitri Poddighe; Kaisar Dauyey
Journal:  Rheumatol Int       Date:  2019-09-16       Impact factor: 2.631

Review 4.  Juvenile idiopathic arthritis: new insights into classification, measures of outcome, and pharmacotherapy.

Authors:  Michael W Beresford
Journal:  Paediatr Drugs       Date:  2011-06-01       Impact factor: 3.022

5.  Hemophagocytic syndrome secondary to adult-onset Still's disease but very similar to lymphoma.

Authors:  Xin-Hua Zhang; Yong-Mei Han; Wen-Wen Wang; Hao Cheng; Ke-Jian Zhu
Journal:  Int J Clin Exp Pathol       Date:  2012-04-16

6.  Association of IRF5 polymorphisms with susceptibility to hemophagocytic lymphohistiocytosis in children.

Authors:  Masakatsu Yanagimachi; Hiroaki Goto; Takako Miyamae; Keisuke Kadota; Tomoyuki Imagawa; Masaaki Mori; Hidenori Sato; Ryu Yanagisawa; Tetsuji Kaneko; Satoshi Morita; Eiichi Ishii; Shumpei Yokota
Journal:  J Clin Immunol       Date:  2011-09-04       Impact factor: 8.317

Review 7.  Regulatory NK-cell functions in inflammation and autoimmunity.

Authors:  Anna Lünemann; Jan D Lünemann; Christian Münz
Journal:  Mol Med       Date:  2009-05-11       Impact factor: 6.354

Review 8.  Horror autoinflammaticus: the molecular pathophysiology of autoinflammatory disease (*).

Authors:  Seth L Masters; Anna Simon; Ivona Aksentijevich; Daniel L Kastner
Journal:  Annu Rev Immunol       Date:  2009       Impact factor: 28.527

9.  Steroid-refractory severe hepatic failure in adult onset Still's disease responding to cyclosporine.

Authors:  Takao Nagashima; Yoko Aoki; Sachiko Onishi; Masahiro Iwamoto; Hitoaki Okazaki; Seiji Minota
Journal:  Clin Rheumatol       Date:  2008-07-01       Impact factor: 3.650

Review 10.  Macrophage activation syndrome: A diagnostic challenge (Review).

Authors:  Anca Bojan; Andrada Parvu; Iulia-Andrea Zsoldos; Tunde Torok; Anca Daniela Farcas
Journal:  Exp Ther Med       Date:  2021-06-24       Impact factor: 2.447

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