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10.5812/ircmj.29249 http://scihub22266oqcxt.onion/10.5812/ircmj.29249 C4867362!4867362 !27195144     free     free     free Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\27195144 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Iran+Red+Crescent+Med+J 2016 ; 18 (2 ): e29249 Nephropedia Template TP {{tp|p=27195144 |t=2016. Idiopathic Systemic Capillary Leak Syndrome: A Case Report |pdf=|usr=}}{{27195144 }} gab.com Text Idiopathic Systemic Capillary Leak Syndrome: A Case Report JO: Iran Red Crescent Med J http://www.kidney.de/pget.php?&tw=1&pmid=27195144 #FOAvip INTRODUCTION: Idiopathic systemic capillary leak syndrome (ISCLS) is rarely seen, and presents with recurrent episodes of hypotension, shock, hemoconcentration, and hypoproteinemia. The main pathology is the dysfunction of the vascular endothelium, and it is characterized by an increase of capillary permeability that is accompanied by the loss of intravascular fluid and protein. CASE PRESENTATION: We present a 58-year-old female who presented with peripheral edema, leg pain, and syncope at the emergency department. Interestingly demyemilising neuropathy, which is a rare finding, ensued on day 4. She is still being treated using intravenous immunoglobulin therapy. CONCLUSIONS: The early signs and symptoms of ISCLS may be subtle; therefore the diagnosis can easily be missed and prompt treatment of the syndrome may be postponed. Thus, the clinician must consider ISCLS in differential diagnosis in cases of hypotension, hemoconcentration, and hypoalbuminemia. Twit Text FOAVip Idiopathic Systemic Capillary Leak Syndrome: A Case Report ????Iran Red Crescent Med J http://www.kidney.de/pget.php?&tw=1&pmid=27195144 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27195144 #FOAvip English Wikipedia <ref>{{Cite pmid|27195144 }}</ref> Idiopathic Systemic Capillary Leak Syndrome: A Case Report #MMPMID27195144 Yardimci B ; Kazancioglu R Iran Red Crescent Med J 2016[Feb]; 18 (2 ): e29249 PMID27195144 show ga INTRODUCTION: Idiopathic systemic capillary leak syndrome (ISCLS) is rarely seen, and presents with recurrent episodes of hypotension, shock, hemoconcentration, and hypoproteinemia. The main pathology is the dysfunction of the vascular endothelium, and it is characterized by an increase of capillary permeability that is accompanied by the loss of intravascular fluid and protein. CASE PRESENTATION: We present a 58-year-old female who presented with peripheral edema, leg pain, and syncope at the emergency department. Interestingly demyemilising neuropathy, which is a rare finding, ensued on day 4. She is still being treated using intravenous immunoglobulin therapy. CONCLUSIONS: The early signs and symptoms of ISCLS may be subtle; therefore the diagnosis can easily be missed and prompt treatment of the syndrome may be postponed. Thus, the clinician must consider ISCLS in differential diagnosis in cases of hypotension, hemoconcentration, and hypoalbuminemia. äIdiopathic Systemic Capillary Leak Syndrome: A Case Report (epmc).pdf DeepDyve Pubget Overpricing