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10.1155/2016/8957690 http://scihub22266oqcxt.onion/10.1155/2016/8957690 C4769753!4769753!26981305     free     free     free Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Case+Rep+Rheumatol 2016 ; 2016 (ä): ä Nephropedia Template TP {{tp|p=26981305|t=2016. An Unusual Case of Systemic Lupus Erythematosus and Hemophagocytic Syndrome |pdf=|usr=}}{{26981305}} gab.com Text An Unusual Case of Systemic Lupus Erythematosus and Hemophagocytic Syndrome JO: Case Rep Rheumatol http://www.kidney.de/pget.php?&tw=1&pmid=26981305 #FOAvip Hemophagocytic syndrome (HS) or hemophagocytic lymphohistiocytosis (HLH) is an immune mediated phenomenon that can occur in the setting of an autoimmune disease, chronic immunosuppression, malignancy, or infection. It has been more commonly described in the pediatric population and less commonly in adults. We describe a case of a 52-year-old male who presented with a rash. He simultaneously met the Systemic Lupus International Collaborating Clinics (SLICC) criteria for the diagnosis of systemic lupus erythematosus (SLE) and the diagnostic criteria of HS as described in the hemophagocytic lymphohistiocytosis (HLH) 2004 trial. The bone marrow on autopsy showed the presence of abundant hemosiderophages with focal hemophagocytosis. SLE-associated HS might be underdiagnosed due to the overlap in clinical findings. This case represents the importance of prompt diagnosis and treatment of such a potentially fatal clinical syndrome. Twit Text FOAVip An Unusual Case of Systemic Lupus Erythematosus and Hemophagocytic Syndrome ????Case Rep Rheumatol http://www.kidney.de/pget.php?&tw=1&pmid=26981305 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26981305 #FOAvip English Wikipedia <ref>{{Cite pmid|26981305}}</ref> An Unusual Case of Systemic Lupus Erythematosus and Hemophagocytic Syndrome #MMPMID26981305 Sharmeen S; Hussain N Case Rep Rheumatol 2016[]; 2016 (ä): ä PMID26981305show ga Hemophagocytic syndrome (HS) or hemophagocytic lymphohistiocytosis (HLH) is an immune mediated phenomenon that can occur in the setting of an autoimmune disease, chronic immunosuppression, malignancy, or infection. It has been more commonly described in the pediatric population and less commonly in adults. We describe a case of a 52-year-old male who presented with a rash. He simultaneously met the Systemic Lupus International Collaborating Clinics (SLICC) criteria for the diagnosis of systemic lupus erythematosus (SLE) and the diagnostic criteria of HS as described in the hemophagocytic lymphohistiocytosis (HLH) 2004 trial. The bone marrow on autopsy showed the presence of abundant hemosiderophages with focal hemophagocytosis. SLE-associated HS might be underdiagnosed due to the overlap in clinical findings. This case represents the importance of prompt diagnosis and treatment of such a potentially fatal clinical syndrome. äAn Unusual Case of Systemic Lupus Erythematosus and Hemophagocytic Syn(epmc).pdf DeepDyve Pubget Overpricing