Vasculitis - Vaskulitis
☆ In die 2022 Stiftung Warentest-resultate van Duitsland was verbruikerstevredenheid met ModelDerm net effens laer as met betaalde telemedisyne-konsultasies.
Ander sistemiese afwykings (outo-immuun siektes) wat vaskulitis behels, moet uitgesluit word.
Dit is 'n tipiese prentjie van vaskulitis van die been. 'n Urinetoets kan gedoen word om te kyk vir abnormaliteite in nierfunksie.
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 'n tipe velontsteking wat klein bloedvate in die vel se diep lae aantas. Dit kan gebeur vir geen bekende rede of gekoppel word aan infeksies, gewasse, outo-immuun siektes, of medikasie. Tipiese tekens sluit in rooi of pers kolle op die bene, betrokkenheid van klein vate, en in ongeveer 30 persent van die gevalle word ander dele van die liggaam ook aangetas. Die meeste gevalle kom vanself binne 'n paar weke tot maande op. Behandeling wissel na gelang van hoe ernstig dit is, van die geleidelike vermindering van orale kortikosteroïede tot die gebruik van ander middels wat inflammasie verlaag sonder steroïede.
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.
○ Diagnose
Vaskulitis beperk tot die vel kan mettertyd verbeter. Bloed- en urinetoetse kan egter gedoen word om sistemiese of outo-immuunafwykings op te spoor.
○ Behandeling ― OTC-dwelms
As vaskulitis tot die vel beperk word sonder inval van ander organe, kan 'n steroïedsalf gebruik word.
#OTC steroid ointment