Idiopathic Systemic Capillary Leak Syndrome: A Diagnostic Challenge and Its Management

Journal Title: Journal of Clinical and Diagnostic Research - Year 2017, Vol 11, Issue 10

Abstract

Idiopathic Systemic Capillary Leak Syndrome (ISCLS) is a fatal disorder characterised by recurrent episodes of hypotension, hypoalbuminemia and haemoconcentration. It is a rare disease, under-reported partly because of unawareness of treating physician. Here is a description of a 30 year old male presenting with history of fever, generalized oedema progressing to hypovolemic shock and multi organ dysfunction. His laboratory studies showed haemoconcentration, hypoalbuminemia and monoclonal gammopathy with negative bacteriological cultures. After excluding other probable etiologies he was diagnosed to have ISCLS. He was managed successfully with intravenous methylprednisolone, theophylline and other supportive measures. He has been put on prophylactic oral theophylline for one year.

Authors and Affiliations

Janak Tarun Bahirwani, Raja Naga Mahesh Maddala, Weena Stanley, Mukhyaprana Prabhu

Keywords

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  • EP ID EP364833
  • DOI 10.7860/JCDR/2017/31384.10707
  • Views 60
  • Downloads 0

How To Cite

Janak Tarun Bahirwani, Raja Naga Mahesh Maddala, Weena Stanley, Mukhyaprana Prabhu (2017). Idiopathic Systemic Capillary Leak Syndrome: A Diagnostic Challenge and Its Management. Journal of Clinical and Diagnostic Research, 11(10), 1-2. https://europub.co.uk/articles/-A-364833