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10.4322/acr.2014.044 http://scihub22266oqcxt.onion/10.4322/acr.2014.044 C4608169!4608169!26484319     free     free     free Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Autops+Case+Rep 2015 ; 5 (1): 11-9 Nephropedia Template TP {{tp|p=26484319|t=2015. Hemophagocytic syndrome: a dilemma chasing the intensivists |pdf=|usr=}}{{26484319}} gab.com Text Hemophagocytic syndrome: a dilemma chasing the intensivists JO: Autops Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=26484319 #FOAvip Hemophagocytic lymphohistiocytosis or hemophagocytic syndrome is represented by an uncontrolled inflammatory response characterized by marked histiocyte activation and a cytokine storm. The entity may present a primary or genetic type, and the secondary type is usually triggered by infectious diseases of any kind, autoimmune disease, or neoplasia. This entity, although well described and with definite diagnostic criteria, still remains misdiagnosed because of the overlap presentation with other inflammatory processes. The authors present the case of a 13-year-old girl who was submitted to an appendicectomy complicated with a pericolic abscess, which required a second operation in order to be drained surgically. During the postoperative period of this second surgical procedure, the patient remained febrile, developing cytopenias, and multiple organ failure. Unfortunately, she died despite the efforts of the intensive care staff. The autopsy findings were characteristic of hemophagocytic syndrome. The authors report the case to call attention to this diagnosis whenever unexpected outcomes of infections are experienced. Twit Text FOAVip Hemophagocytic syndrome: a dilemma chasing the intensivists ????Autops Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=26484319 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26484319 #FOAvip English Wikipedia <ref>{{Cite pmid|26484319}}</ref> Hemophagocytic syndrome: a dilemma chasing the intensivists #MMPMID26484319 Queiroz AF; Benevides GN; Fernandes Ide COF; Goes Pde F; Bousso A; Ferreira CR Autops Case Rep 2015[Jan]; 5 (1): 11-9 PMID26484319show ga Hemophagocytic lymphohistiocytosis or hemophagocytic syndrome is represented by an uncontrolled inflammatory response characterized by marked histiocyte activation and a cytokine storm. The entity may present a primary or genetic type, and the secondary type is usually triggered by infectious diseases of any kind, autoimmune disease, or neoplasia. This entity, although well described and with definite diagnostic criteria, still remains misdiagnosed because of the overlap presentation with other inflammatory processes. The authors present the case of a 13-year-old girl who was submitted to an appendicectomy complicated with a pericolic abscess, which required a second operation in order to be drained surgically. During the postoperative period of this second surgical procedure, the patient remained febrile, developing cytopenias, and multiple organ failure. Unfortunately, she died despite the efforts of the intensive care staff. The autopsy findings were characteristic of hemophagocytic syndrome. The authors report the case to call attention to this diagnosis whenever unexpected outcomes of infections are experienced. äHemophagocytic syndrome: a dilemma chasing the intensivists (epmc).pdf DeepDyve Pubget Overpricing