Exceptional association of hypocomplementemic urticarial vasculitis syndrome (HUVS) and symptomatic pulmonary histoplasmosis: a case-based literature review
Sign Up to like & getrecommendations! Published in 2019 at "Clinical Rheumatology"
DOI: 10.1007/s10067-019-04548-8
Abstract: Hypocomplementemic urticarial vasculitis syndrome (HUVS) is a rare type III hypersensitivity disorder characterized by urticarial vasculitis and prolonged hypocomplementemia. Individuals with HUVS may also have joint involvement, pulmonary manifestations, ocular disease, kidney inflammation, or any… read more here.
Keywords: huvs; hypocomplementemic urticarial; vasculitis syndrome; urticarial vasculitis ... See more keywords
Hypocomplementemic urticarial vasculitis syndrome associated with rapidly progressive glomerulonephritis: lessons for the clinical nephrologist
Sign Up to like & getrecommendations! Published in 2021 at "Journal of Nephrology"
DOI: 10.1007/s40620-020-00942-7
Abstract: A 34year-old Hispanic woman with a past medical history of obesity presented with a 2-day history of epigastric abdominal pain accompanied by nausea and vomiting, arthralgias, periorbital edema and a flat, erythematous, pruritic bilateral rash… read more here.
Keywords: syndrome associated; creatinine; hypocomplementemic urticarial; vasculitis syndrome ... See more keywords