Literature DB >> 28979438

Haemophagocytic syndrome in intensive care: The great pretender.

Ignacio de Asua1, Esteban Ciliberti1.   

Abstract

The haemophagocytic syndrome is a unique disease process in which the dysregulation of the patient's immune system leads to an inflammatory storm which rapidly ravages through multiple organ systems, generating life-threatening end-organ dysfunction. Since it usually mimics other conditions frequently encountered in the critical care population - most notably septic shock - its diagnosis is elusive and the condition remains under-recognized and under-reported. We present a concise review of the pathophysiology and clinical features of the heamophagocytic syndrome and discuss the main diagnostic and therapeutic issues relevant to the management of this condition in the critically ill patient. Increasing awareness about the haemophagocytic syndrome amongst intensive care physicians will facilitate earlier recognition and timely management.

Entities:  

Keywords:  Lymphohistiocytosis; haemophagocytic; histiocytic disorders; histiocytosis

Year:  2015        PMID: 28979438      PMCID: PMC5606461          DOI: 10.1177/1751143715584383

Source DB:  PubMed          Journal:  J Intensive Care Soc        ISSN: 1751-1437


  13 in total

Review 1.  Approach to hemophagocytic syndromes.

Authors:  Sheila Weitzman
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2011

2.  Prognostic factors of early death in a cohort of 162 adult haemophagocytic syndrome: impact of triggering disease and early treatment with etoposide.

Authors:  Marc Arca; Laurence Fardet; Lionel Galicier; Sébastien Rivière; Christophe Marzac; Cédric Aumont; Olivier Lambotte; Paul Coppo
Journal:  Br J Haematol       Date:  2014-08-26       Impact factor: 6.998

3.  Bone marrow assessment in the diagnosis of acquired hemophagocytic lymphohistiocytosis in adults.

Authors:  Maciej Machaczka; Monika Klimkowska
Journal:  Am J Clin Pathol       Date:  2015-02       Impact factor: 2.493

Review 4.  Apoptotic cell clearance: basic biology and therapeutic potential.

Authors:  Ivan K H Poon; Christopher D Lucas; Adriano G Rossi; Kodi S Ravichandran
Journal:  Nat Rev Immunol       Date:  2014-01-31       Impact factor: 53.106

Review 5.  Contemporary diagnostic methods for hemophagocytic lymphohistiocytic disorders.

Authors:  Theodore S Johnson; Joyce Villanueva; Alexandra H Filipovich; Rebecca A Marsh; Jack J Bleesing
Journal:  J Immunol Methods       Date:  2010-11-24       Impact factor: 2.303

6.  Clinical characteristics, prognostic factors, and outcomes of adult patients with hemophagocytic lymphohistiocytosis.

Authors:  Zaher K Otrock; Charles S Eby
Journal:  Am J Hematol       Date:  2015-01-16       Impact factor: 10.047

Review 7.  Adult haemophagocytic syndrome.

Authors:  Manuel Ramos-Casals; Pilar Brito-Zerón; Armando López-Guillermo; Munther A Khamashta; Xavier Bosch
Journal:  Lancet       Date:  2013-11-27       Impact factor: 79.321

Review 8.  Diagnostic evaluation of patients with suspected haemophagocytic lymphohistiocytosis.

Authors:  Kai Lehmberg; Stephan Ehl
Journal:  Br J Haematol       Date:  2012-12-04       Impact factor: 6.998

9.  Critical care management of patients with hemophagocytic lymphohistiocytosis.

Authors:  Sophie Buyse; Luis Teixeira; Lionel Galicier; Eric Mariotte; Virginie Lemiale; Amélie Seguin; Philippe Bertheau; Emmanuel Canet; Adrienne de Labarthe; Michaël Darmon; Michel Rybojad; Benoit Schlemmer; Elie Azoulay
Journal:  Intensive Care Med       Date:  2010-06-08       Impact factor: 17.440

10.  Reactive hemophagocytic syndrome in adult-onset Still disease: clinical features, predictive factors, and prognosis in 21 patients.

Authors:  Chang-Bum Bae; Ju-Yang Jung; Hyoun-Ah Kim; Chang-Hee Suh
Journal:  Medicine (Baltimore)       Date:  2015-01       Impact factor: 1.889

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