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dc.contributor.authorYARDIMCI, Bulent
dc.contributor.authorKazancioglu, RÜMEYZA
dc.date.accessioned2019-10-05T14:55:18Z
dc.date.available2019-10-05T14:55:18Z
dc.date.issued2016-02-01
dc.identifier10.1097/00000637-199911000-00002
dc.identifier.urihttps://hdl.handle.net/20.500.12645/5065
dc.description.abstractIntroduction: 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.en
dc.language.isoen
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.subjectYARDIMCI B., Kazancioglu R., -Idiopathic Systemic Capillary Leak Syndrome: A Case Report-, IRANIAN RED CRESCENT MEDICAL JOURNAL, cilt.18, 2016
dc.titleIdiopathic Systemic Capillary Leak Syndrome: A Case Report
dc.typeArticle
local.avesis.response4935
local.article.journalnameANNALS OF PLASTIC SURGERY
dc.identifier.wosWOS:000376141200024
dc.identifier.scopus84957542564
dc.identifier.doi10.5812/ircmj.29249
dc.identifier.pubmed27195144
local.publication.isinternational1


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