Vasculitis
☆ Yn 'e 2022 Stiftung Warentest-resultaten út Dútslân wie de konsuminttefredenheid mei ModelDerm mar wat leger dan mei betelle telemedisynkonsultaasjes.
Oare systemyske steuringen (autoimmune sykten) mei vasculitis moatte wurde útsletten.
Dit is in typysk byld fan vasculitis fan 'e skonk. In urinetest kin dien wurde om te kontrolearjen op abnormaliteiten yn 'e nierfunksje.
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 is in soarte fan hûdûntstekking dy't ynfloed hat op lytse bloedfetten yn 'e djippe lagen fan 'e hûd. It kin barre sûnder bekende reden of wurde keppele oan ynfeksjes, tumors, autoimmune sykten, of medisinen. Typyske tekens omfetsje reade of pearse flekken op 'e skonken, belutsenens fan lytse skippen, en yn sawat 30 prosint fan' e gefallen binne oare dielen fan it lichem ek beynfloede. De measte gefallen ferdwine op har eigen binnen in pear wiken oant moannen. Behanneling ferskilt basearre op hoe slim it is, fan stadichoan ferminderjen fan orale corticosteroids oant it brûken fan oare medisinen dy't de ûntstekking ferleegje sûnder steroïden.
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.
○ Diagnoaze
Vasculitis beheind ta de hûd kin oer tiid ferbetterje. Bloed- en urinetests kinne lykwols dien wurde om systemyske of autoimmune steuringen te detektearjen.
○ Behanneling ― OTC Drugs
As vasculitis beheind is ta de hûd sûnder ynvaazje fan oare organen, kin in steroide salve brûkt wurde.
#OTC steroid ointment