Management of Acute Episodes of Clarkson Disease (Monoclonal Gammopathy-Associated Systemic Capillary Leak Syndrome) With Intravenous Immunoglobulins.
Blood plasma
Capillaries
Edema
Intravenous immunoglobulin
Retrospective studies
Shock
Systemic diseases
Journal
Annals of internal medicine. Clinical cases
ISSN: 2767-7664
Titre abrégé: Ann Intern Med Clin Cases
Pays: United States
ID NLM: 9918419285506676
Informations de publication
Date de publication:
Aug 2022
Aug 2022
Historique:
entrez:
19
9
2022
pubmed:
20
9
2022
medline:
20
9
2022
Statut:
ppublish
Résumé
Monoclonal gammopathy-associated idiopathic systemic capillary leak syndrome (ISCLS, Clarkson disease) is a rare disorder defined by transient but recurrent bouts of hypotensive shock and anasarca resulting from plasma extravasation. Although prophylactic treatment with high-dose intravenous immunoglobulins (IVIG, 1-2 g/kg/mo) prevents most disease flares, its utility for acute episodes of ISCLS is unclear. Here, we report the results of a retrospective study of subjects with acute ISCLS treated at or near the onset of symptoms with IVIG. We found that administration of IVIG with minimal additional intravenous fluids was safe and associated with rapid clinical improvement. IVIG given close to the onset of ISCLS-related symptoms is associated with a favorable outcome.
Identifiants
pubmed: 36119848
doi: 10.7326/aimcc.2022.0496
pmc: PMC9481058
mid: NIHMS1835743
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : Intramural NIH HHS
ID : ZIA AI001083
Pays : United States
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