Results 161 to 170 of about 260,356 (192)
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[Macrophage activation syndrome].

La Revue du praticien, 2005
Macrophage 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
openaire   +1 more source

Rowell syndrome complicated with macrophage activation syndrome in a child

Lupus, 2019
Rowell syndrome (RS) is a rare disease characterized by the association of systemic lupus erythematosus (SLE) or cutaneous lupus with lesions similar to erythema multiforme and the presence of autoantibodies including ANA, SSA, SSB, or rheumatoid factor. Due to the low incidence of this disease, the epidemiology of RS is not clear. So far there are 95
I Aguirre-Martinez   +6 more
openaire   +2 more sources

Etanercept for therapy‐resistant macrophage activation syndrome

Pediatric Blood & Cancer, 2006
AbstractMacrophage 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
openaire   +4 more sources

Macrophage activation syndromes.

Nouvelle revue francaise d'hematologie, 1993
The 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
openaire   +1 more source

Macrophage activation syndrome.

The Journal of the Association of Physicians of India, 2006
Macrophage 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
openaire   +1 more source

[The hemophagocytic syndrome (macrophage activation syndrome)].

Minerva medica, 2003
The 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
openaire   +1 more source

[Macrophage activation syndrome, hemophagocytic syndrome].

Pathologie-biologie, 2004
Macrophage 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
openaire   +1 more source

Macrophage Activation in the Acquired Immunodeficiency Syndrome

1988
In view of the clear documentation that T-cell function in the acquired immunodefiency syndrome (AIDS) is grossly impaired, the striking susceptibility of AIDS patients to infections caused by intracellular micro-organisms is not only not surprising but is predictable.
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Macrophage activation syndrome in pediatric Sjögren's syndrome

Seminars in Arthritis and Rheumatism, 2022
Ezgi Deniz Batu   +3 more
openaire   +2 more sources

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