Hypocomplementemic urticarial vasculitis syndrome with severe systemic manifestations
Identifieur interne : 002C82 ( Main/Exploration ); précédent : 002C81; suivant : 002C83Hypocomplementemic urticarial vasculitis syndrome with severe systemic manifestations
Auteurs : Alberto Martini ; Angelo Ravelli ; Salvatore Albani ; Fabrizio De Benedetti ; Margherita Massa ; Jeffrey J. WisnieskiSource :
- The Journal of Pediatrics [ 0022-3476 ] ; 1994.
English descriptors
- KwdEn :
- Teeft :
- Anticardiolipin antibodies, Antineutrophil cytoplasmic antibody, Arthralgia, Benign disease, Blood urea nitrogen, Carattere scientifico, Chest roentgenogram, Clin, Cutaneous, Dapsone, Erythematosus, Erythrocyte sedimentation rate, Glomerulonephritis, Goodpasture syndrome, Hemoglobin concentration, Hemoglobin level, Hemoglobin value, Huvs, Hypocomplementemic, Hypocomplementemic urticarial vasculitis syndrome, Joint manifestations, Lesion, Lung bases, Lupus, Mayo clin proc, Other diseases, Papillary dermis, Pavia, Pediatrics, Polyarteritis nodosa, Prednisone therapy, Pulmonary disease, Pulmonary hemorrhage, Renal, Renal function, Rheumatoid factor, Roentgenogram, Serum concentrations, Surface antigen, Syndrome, Systemic lupus erythematosus, Urinalysis, Urticarial, Urticarial lesion, Urticarial lesions, Urticarial vasculitis, Vasculitis.
Abstract
Abstract: We describe two children with clinical and laboratory features of hypocomplementemic urticarial vasculitis syndrome. Both patients had severe, life-threatening manifestations: rapidly progressive glomerulonephritis (patient 1) and pulmonary hemorrhage (patient 2). We conclude that this syndrome may be a potentially severe multisystem disease. (J PEDIATR 1994;124:742-4)
Url:
DOI: 10.1016/S0022-3476(05)81367-8
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Abstract: We describe two children with clinical and laboratory features of hypocomplementemic urticarial vasculitis syndrome. Both patients had severe, life-threatening manifestations: rapidly progressive glomerulonephritis (patient 1) and pulmonary hemorrhage (patient 2). We conclude that this syndrome may be a potentially severe multisystem disease. (J PEDIATR 1994;124:742-4)</div>
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<tree><noCountry><name sortKey="Albani, Salvatore" sort="Albani, Salvatore" uniqKey="Albani S" first="Salvatore" last="Albani">Salvatore Albani</name>
<name sortKey="De Benedetti, Fabrizio" sort="De Benedetti, Fabrizio" uniqKey="De Benedetti F" first="Fabrizio" last="De Benedetti">Fabrizio De Benedetti</name>
<name sortKey="Martini, Alberto" sort="Martini, Alberto" uniqKey="Martini A" first="Alberto" last="Martini">Alberto Martini</name>
<name sortKey="Massa, Margherita" sort="Massa, Margherita" uniqKey="Massa M" first="Margherita" last="Massa">Margherita Massa</name>
<name sortKey="Ravelli, Angelo" sort="Ravelli, Angelo" uniqKey="Ravelli A" first="Angelo" last="Ravelli">Angelo Ravelli</name>
<name sortKey="Wisnieski, Jeffrey J" sort="Wisnieski, Jeffrey J" uniqKey="Wisnieski J" first="Jeffrey J." last="Wisnieski">Jeffrey J. Wisnieski</name>
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