Hypokomplementämisches Urtikaria-Vaskulitis-Syndrom
Identifieur interne : 001B98 ( Main/Exploration ); précédent : 001B97; suivant : 001B99Hypokomplementämisches Urtikaria-Vaskulitis-Syndrom
Auteurs : P. Staubach-Renz [Allemagne] ; E. Von Stebut [Allemagne] ; W. Br Uninger [Allemagne] ; M. Maurer [Allemagne] ; K. Steinbrink [Allemagne]Source :
- Der Hautarzt [ 0017-8470 ] ; 2007-08-01.
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Abstract
Zusammenfassung: Autoimmunerkrankungen können klinisch unter dem Bild einer therapierefraktären chronischen Urtikaria (CU) auftreten. Der vorliegende Fall schildert den Verlauf bei einem Patienten mit hypokomplementämischem Urtikaria-Vaskulitis-Syndrom (HUVS) und den schnellen Behandlungserfolg mit hoch dosierten intravenösen Immunglobulinen (IVIG). Die Diagnose wurde klinisch gestellt und histologisch sowie laborchemisch gesichert. Bereits nach einem Zyklus mit IVIG (2 g/kg/Körpergewicht) waren alle Symptome deutlich rückläufig.
Abstract: Autoimmune diseases can initially present as chronic urticaria. We describe the course of a patient with hypocomplementemic urticarial vasculitis syndrome (HUVS) as well as his successful treatment with high-dose intravenous immunoglobulins (IVIG). HUVS was diagnosed clinically and confirmed by histology and laboratory studies. After only one cycle with IVIG (2 g/kg) all HUVS symptoms were significantly decreased.
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DOI: 10.1007/s00105-007-1301-5
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Der vorliegende Fall schildert den Verlauf bei einem Patienten mit hypokomplementämischem Urtikaria-Vaskulitis-Syndrom (HUVS) und den schnellen Behandlungserfolg mit hoch dosierten intravenösen Immunglobulinen (IVIG). Die Diagnose wurde klinisch gestellt und histologisch sowie laborchemisch gesichert. Bereits nach einem Zyklus mit IVIG (2 g/kg/Körpergewicht) waren alle Symptome deutlich rückläufig.</div><div type="abstract" xml:lang="en">Abstract: Autoimmune diseases can initially present as chronic urticaria. We describe the course of a patient with hypocomplementemic urticarial vasculitis syndrome (HUVS) as well as his successful treatment with high-dose intravenous immunoglobulins (IVIG). HUVS was diagnosed clinically and confirmed by histology and laboratory studies. After only one cycle with IVIG (2 g/kg) all HUVS symptoms were significantly decreased.</div></front></TEI><affiliations><list><country><li>Allemagne</li></country><region><li>Berlin</li></region><settlement><li>Berlin</li></settlement></list><tree><country name="Allemagne"><noRegion><name sortKey="Staubach Renz, P" sort="Staubach Renz, P" uniqKey="Staubach Renz P" first="P." last="Staubach-Renz">P. Staubach-Renz</name></noRegion><name sortKey="Br Uninger, W" sort="Br Uninger, W" uniqKey="Br Uninger W" first="W." last="Br Uninger">W. Br Uninger</name><name sortKey="Maurer, M" sort="Maurer, M" uniqKey="Maurer M" first="M." last="Maurer">M. Maurer</name><name sortKey="Maurer, M" sort="Maurer, M" uniqKey="Maurer M" first="M." last="Maurer">M. Maurer</name><name sortKey="Staubach Renz, P" sort="Staubach Renz, P" uniqKey="Staubach Renz P" first="P." last="Staubach-Renz">P. 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