Idiopathic systemic capillary leak syndrome – An often missed diagnosis.
- Senior PG Registrar, Department of Endocrinology and Metabolism, Christian Medical College, Vellore, India.
- Associate Professor, Department of Endocrinology and Metabolism, Christian Medical College, Vellore, India.
- Professor, Department of Endocrinology and Metabolism, Christian Medical College, Vellore, India.
Tropical doctor Vol. 51 · Issue 2 · pp. 246-248
PMID 33349162 DOI 10.1177/0049475520979299
Cite This Article
Remya Rajan, Nitin Kapoor, Hesarghatta S Asha, Thomas V Paul, Nihal Thomas. Idiopathic systemic capillary leak syndrome – An often missed diagnosis. Tropical doctor. 2021;51(2):246-248. doi:10.1177/0049475520979299
Abstract
Idiopathic systemic capillary leak syndrome (ISCLS) is a potentially fatal disorder characterised by 'attacks' of varying intensity of hypovolemic shock in association with haemoconcentration and hypoalbuminaemia. It is a disease of exclusion, and the severity of attacks may mimic sepsis at presentation. We report a case of a lady with recurrent attacks of ISCLS with at least two life-threatening episodes, having been treated elsewhere as a case of steroid insufficiency. The diagnosis is often challenging, and treatment of an acute episode involves the judicious use of fluids and vasopressors, as required. Prophylaxis to prevent further attacks is of varied success.
Keywords
- IVIG
- Systemic capillary leak syndrome
- episodic hemoconcentration
- recurrent hypovolumic shock




