Vasculitis
☆ Natiijooyinka Stiftung Warentest ee 2022 ee ka yimid Jarmalka, ku qanacsanaanta macaamilka ee ModelDerm ayaa waxyar uun ka hooseysay la-talinta telemedicine-ka ee lacagta lagu bixiyo.
Xanuunada kale ee habdhiska (autoimmune disease) ee ku lug leh vasculitis waa in meesha laga saaro.
Tani waa sawirka caadiga ah ee vasculitis ee lugta. Baaritaanka kaadida ayaa la samayn karaa si loo hubiyo cilladaha shaqada kelyaha.
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 waa nooc ka mid ah caabuqa maqaarka ee saameeya xididada yaryar ee dhiiga ee lakabyada qoto dheer ee maqaarka. Waxay ku dhici kartaa sabab la'aan ama waxay ku xiran tahay caabuqyada, burooyinka, cudurada difaaca jirka, ama daawooyinka. Calaamadaha caadiga ah waxaa ka mid ah baro casaan ama casaan ah oo lugaha ah, ku lug lahaanshaha maraakiibta yaryar, iyo qiyaastii 30 boqolkiiba kiisaska, qaybaha kale ee jirka ayaa sidoo kale saameeya. Kiisaska intooda badani waxay iskood ku soo baxaan dhawr toddobaad ilaa bilo gudahood. Daaweyntu way kala duwan tahay iyadoo lagu saleynayo sida ay u daran tahay, laga bilaabo si tartiib tartiib ah loo yareeyo corticosteroids afka ilaa isticmaalka dawooyinka kale ee hoos u dhigaya bararka aan lahayn steroids.
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.
○ Cilmiga
Vasculitis ku xaddidan maqaarka ayaa laga yaabaa inay soo fiicnaato waqti ka dib. Si kastaba ha ahaatee, baaritaanada dhiigga iyo kaadida ayaa laga yaabaa in la sameeyo si loo ogaado cilladaha habdhiska ama difaaca jirka.
○ Daawaynta - Daawooyinka OTC
Haddii vasculitis uu ku kooban yahay maqaarka iyada oo aan la soo qaadin xubnaha kale, boomaatada steroid ayaa la isticmaali karaa.
#OTC steroid ointment