The systemic capillary-leak syndrome (SCLS), also known as Clarkson's disease, is a rare condition characterized by recurrent episodes of capillary hyperpermeability in the context of a monoclonal gammopathy.1 We have previously shown that prophylactic treatment with intravenous immunoglobulins (IVIg) significantly reduces relapse and improves survival.2,3 SCLS episodes are thought to have an infectious trigger, especially mediated by viruses, and a flu-like viral syndrome was reported in more than half of the episodes in a large cohort of Clarkson's disease flares.
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Chambrun et al. (2020) studied this question.
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