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Macrophage activation syndromes.
Nouvelle revue francaise d'hematologie, 1993The clinical and laboratory features of 47 cases of macrophage activation syndrome (MAS) were reviewed in a workshop within the Groupe Français d'Hématologie cellulaire. There was no predilection for a particular age group, while common symptoms at presentation included fever, hepatic and splenic enlargement and profound depression of blood count ...
A, Albert +9 more
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[Macrophage activation syndrome].
La Revue du praticien, 2005Macrophage activation syndrome is due to macrophage stimulation secondary to excessive cytokine secretion. Infectious (mainly viral) and neoplastic (lymphomas primarily) diseases are the mainly triggering circumstances of this syndrome associated with immunodepression.
Olivier, Fain, Jérôme, Stirnemann
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Scrub typhus associated macrophage activation syndrome
Tropical Doctor, 2010Macrophage activation syndrome (MAS) is a rare phenomenon that occurs either primarily or secondary to a multitude of conditions, including juvenile rheumatoid arthritis most commonly, and other infections like enteric fever and tuberculosis. It has been reported as an extremely rare complication of scrub typhus with no cases presented from India.
Gopinath Kango, Gopal +2 more
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Macrophage activation syndrome.
The Journal of the Association of Physicians of India, 2006Macrophage Activation Syndrome is a rare and potentially fatal disease, to be considered in patients with a SIRS like clinical presentation. Falling ESR and hyperferritinemia in the appropriate clinical setting can be the greatest clues. We report a case in which a female admitted with fever and rash, initially had systemic inflammatory response ...
M K, Kumar, M K, Suresh, D, Dalus
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Kawasaki disease shock syndrome and macrophage activation syndrome
Paediatrics and International Child Health, 2018We thank Han and Lee [1] for their comments and interest in our case report [2]. They report a patient similar to ours in terms of clinical presentations but who had a final diagnosis of Kawasaki d...
Hui-Fang Yang, Hueng-Chuen Fan
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Etanercept for therapy‐resistant macrophage activation syndrome
Pediatric Blood & Cancer, 2006AbstractMacrophage activation syndrome (MAS) is a severe, potentially fatal complication of childhood rheumatic diseases, especially systemic onset juvenile idiopathic arthritis (SoJIA). We report a 4‐year‐old girl with probable SoJIA who presented with MAS. She did not respond to pulse methyl prednisolone and Cyclosporine A (CsA).
Yilmaz, S. +5 more
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Macrophage Activation Syndrome (MAS)
2019Macrophage activation syndrome (MAS) is a life-threatening systemic immune-mediated condition and a catastrophic complication of autoinflammatory conditions such as adult-onset Still’s disease (AOSD) and systemic juvenile idiopathic arthritis (SJIA). It is a subtype of hemophagocytic lymphohistiocytosis (HLH) associated with underlying rheumatologic ...
Bella Mehta, Petros Efthimiou
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[Macrophage activation syndrome, hemophagocytic syndrome].
Pathologie-biologie, 2004Macrophage activation syndrome MAS describes the clinical, biological and histological symptoms related to a probably T lymphocytes/NK cell driven stimulation of macrophages with the consequence of a hemophagocytosis involving numerous organs, preferentially bone marrow, explaining the other term of "hemophagocytic syndrome".
A, Pradalier +3 more
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[Reactive macrophage activation syndrome].
Orvosi hetilap, 2004Reactive macrophage activation syndrome or haemophagocytic lymphohistiocytosis is a life-threatening immunoregulatory disorder characterized by the activation of the mononuclear phagocytic system with prominent haemophagocytosis particularly involving the bone marrow, reticuloendothelial system and central nervous system.
Szilvia, Szamosi +3 more
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[The hemophagocytic syndrome (macrophage activation syndrome)].
Minerva medica, 2003The hemophagocytic syndrome (HPS) is an uncommon, often misdiagnosed life-threatening disorder of immune regulation, characterized by a widespread proliferation and multisystemic infiltration of non-malignant histiocytes that undergo uncontrolled hemophagocytosis in bone marrow and/or reticulo-endothelial system.
P, Fietta, P, Manganelli
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