Vasculitis - Vaskulitis
☆ An den 2022 Stiftung Warentest Resultater aus Däitschland war d'Zefriddenheet vum Konsument mam ModelDerm nëmme liicht manner wéi mat bezuelte Telemedizin Konsultatiounen.
Aner systemesch Stéierungen (Autoimmunerkrankungen) mat Vaskulitis sollen ausgeschloss ginn.
Dëst ass en typescht Bild vu Vaskulitis vum Been. En Urin Test kann gemaach ginn fir Abnormalitéiten an der Nierfunktioun ze kontrolléieren.
References
Of the 61 patients studied, hypersensitivity vasculitis (HSV) [23 (37.7%)] and Henoch Schonlein purpura (HSP) [16 (26.2%)] were the two most common forms. Systemic involvement was seen in 32 (52.45%) patients. Drugs were implicated in 12 (19.7%) cases, infections in 7 (11.4%) and connective tissue disorders in 4 (6.5%) cases. No association was seen between history of drug intake and tissue eosinophilia and also between histologically severe vasculitis and clinical severity.
Leukocytoclastic vasculitis ass eng Zort Hautentzündung déi kleng Bluttgefässer an den déiwe Schichten vun der Haut beaflosst. Et kann aus kee bekannte Grond geschéien oder mat Infektiounen, Tumoren, Autoimmunerkrankungen oder Medikamenter verbonne sinn. Typesch Schëlder enthalen rout oder purpurroude Flecken op de Been, Bedeelegung vu klenge Schëffer, an ongeféier 30 Prozent vun de Fäll sinn och aner Deeler vum Kierper betraff. Déi meescht Fäll klären sech selwer bannent e puer Wochen bis Méint. D'Behandlung variéiert op Basis vu wéi schwéier et ass, vu gradueller Ofsenkung vun mëndleche Corticosteroiden fir aner Medikamenter ze benotzen déi d'Entzündung senken ouni Steroiden.
Leukocytoclastic vasculitis is a cutaneous, small-vessel vasculitis of the dermal capillaries and venules. This condition can be idiopathic or can be associated with infections, neoplasms, autoimmune disorders, and drugs. Key clinical features of leukocytoclastic vasculitis include palpable purpura on the lower extremity, small vessel involvement, and, in about 30 percent of individuals, extracutaneous involvement. Most cases of idiopathic cutaneous, small vessel vasculitis are self-limited with 90 percent of cases resolving in weeks to months of onset. Otherwise, treatment depends on the severity of disease and can range from an oral corticosteroid taper to various steroid-sparing immunosuppressive agents.
Leukocytoclastic vasculitis is a cutaneous, small-vessel vasculitis of the dermal capillaries and venules. This condition can be idiopathic or can be associated with infections, neoplasms, autoimmune disorders, and drugs. Key clinical features of leukocytoclastic vasculitis include palpable purpura on the lower extremity, small vessel involvement, and, in about 30 percent of individuals, extracutaneous involvement. Most cases of idiopathic cutaneous, small vessel vasculitis are self-limited with 90 percent of cases resolving in weeks to months of onset. Otherwise, treatment depends on the severity of disease and can range from an oral corticosteroid taper to various steroid-sparing immunosuppressive agents.
○ Diagnos
Vasculitis limitéiert op d'Haut kann mat der Zäit verbesseren. Wéi och ëmmer, Blutt an Urin Tester kënne gemaach ginn fir systemesch oder Autoimmunerkrankungen z'entdecken.
○ Behandlung ― OTC Drogen
Wann Vaskulitis op d'Haut limitéiert ass ouni Invasioun vun aneren Organer, kann eng Steroid Salbe benotzt ginn.
#OTC steroid ointment