Vasculitis - Vaskulitis
☆ U rezultatima Stiftung Warentest-a za 2022. iz Njemačke, zadovoljstvo potrošača ModelDerm-om bilo je samo nešto niže nego s plaćenim telemedicinskim konsultacijama.
Treba isključiti druge sistemske poremećaje (autoimune bolesti) koji uključuju vaskulitis.
Ovo je tipična slika vaskulitisa nogu. Test urina može se uraditi kako bi se provjerile abnormalnosti u funkciji bubrega.
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 je vrsta upale kože koja zahvaća male krvne žile u dubokim slojevima kože. To se može dogoditi bez poznatog razloga ili biti povezano s infekcijama, tumorima, autoimunim bolestima ili lijekovima. Tipični znaci uključuju crvene ili ljubičaste mrlje na nogama, zahvaćenost malih krvnih žila, au oko 30 posto slučajeva zahvaćeni su i drugi dijelovi tijela. Većina slučajeva nestaje sama od sebe u roku od nekoliko sedmica do mjeseci. Liječenje varira ovisno o tome koliko je ozbiljno, od postepenog smanjenja oralnih kortikosteroida do korištenja drugih lijekova koji smanjuju upalu bez steroida.
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.
○ Dijagnoza
Vaskulitis ograničen na kožu može se vremenom poboljšati. Međutim, testovi krvi i urina mogu se uraditi kako bi se otkrili sistemski ili autoimuni poremećaji.
○ Liječenje ― OTC lijekovi
Ako je vaskulitis ograničen na kožu bez invazije na druge organe, može se koristiti steroidna mast.
#OTC steroid ointment