Vasculitis - Vasculite
☆ In i risultati Stiftung Warentest 2022 da Germania, a satisfaczione di i cunsumatori cù ModelDerm era solu ligeramente più bassu chè cù cunsultazioni di telemedicina pagate.
L'altri disordini sistemici (malattie autoimmune) chì implicanu vasculitis deve esse esclusi.
Questa hè una stampa tipica di vasculitis di a gamba. Una prova d'urina pò esse fatta per verificà anormalità in a funzione renale.
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 hè un tipu d'infiammazione di a pelle chì affetta i picculi vini sanguini in i strati prufondi di a pelle. Pò accade per nisuna ragione cunnisciuta o esse ligata à infizzioni, tumuri, malatie autoimmune o medicazione. I segni tipici includenu spots rossi o viole nantu à i gammi, implicazione di picculi navi, è in circa 30 per centu di i casi, l'altri parti di u corpu sò ancu affettati. A maiò parte di i casi sbulicà da sè stessu in pochi settimane à mesi. U trattamentu varieghja secondu quantu hè severu, da riduce gradualmente i corticosteroidi orali à l'usu di altre droghe chì diminuiscenu a inflamazioni senza steroidi.
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.
○ Diagnosi
Vasculitis limitata à a pelle pò migliurà cù u tempu. Tuttavia, i testi di sangue è d'urina ponu esse fatti per detectà disordini sistemici o autoimmuni.
○ Trattamentu - Drogi OTC
Se a vasculitis hè limitata à a pelle senza invasione di altri organi, un unguentu steroidu pò esse usatu.
#OTC steroid ointment