Literature DB >> 8796089

[Hemophagocytic syndromes. A series of 23 cases].

M Tiab1, F Mechinaud, M Hamidou, F Gaillard, F Raffi, J L Harousseau.   

Abstract

Inappropriate macrophage activation is responsible for clinical, biological and histological features characterized by diffuse non malignant histiocytic tissue infiltration called "reactive hemophagocytic syndrome" (RHS). We report here 23 new cases. Immunodepression (10 cases), hematologic malignancies (13 cases) and infection (10 cases) are the most favorable conditions associated with RHS. In many cases, several conditions were present at time of diagnosis of RHS and increased its severity. Mechanisms of RHS remains unclear, but cytokine may play a role. Outcome is variable, but death is the most common issue (17 deaths in our series related to RHS). Corticosteroids, etoposide can improve some situations. Further study is needed to establish the role of cyclosporine A or allogenic bone marrow transplantation.

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Year:  1996        PMID: 8796089

Source DB:  PubMed          Journal:  Ann Med Interne (Paris)        ISSN: 0003-410X


  2 in total

1.  Severe hemophagocytic lymphohistiocytosis as a complication of drug-induced hypersensitivity syndrome.

Authors:  Dron Gauchan; Hamid Shaaban; Neil Parikh; Nai-Lun Chang; Zaid Altheeb; Michael Maroules
Journal:  Int J Crit Illn Inj Sci       Date:  2015 Jan-Mar

2.  Hemophagocytic Lymphohistiocytosis in Intensive Care Unit: A 71-Case Strobe-Compliant Retrospective Study.

Authors:  Thomas Barba; Delphine Maucort-Boulch; Jean Iwaz; Julien Bohé; Jacques Ninet; Arnaud Hot; Jean-Christophe Lega; Claude Guérin; Laurent Argaud; Christiane Broussolle; Yvan Jamilloux; Jean-Christophe Richard; Pascal Sève
Journal:  Medicine (Baltimore)       Date:  2015-12       Impact factor: 1.817

  2 in total

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