Vasculitis - Baskulitis
☆ Alemaniako Stiftung Warentest-en 2022ko emaitzetan, ModelDerm-ekin kontsumitzaileen gogobetetasuna apur bat txikiagoa izan zen ordaindutako telemedikuntzako kontsultekin baino.
Baskulitisa dakarren beste nahaste sistemiko batzuk (gaixotasun autoimuneak) baztertu behar dira.
Hau hankako baskulitearen irudi tipikoa da. Gernu‑proba bat egin daiteke giltzurrun‑funtzioan anomaliak daudela egiaztatzeko.
relevance score : -100.0%
ReferencesOf 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 azaleko geruza sakonetako odol-hodi txikiei eragiten dien larruazaleko hantura mota bat da. Arrazoi jakinik gabe gerta daiteke edo infekzioekin, tumoreekin, gaixotasun autoimmuneekin edo botikekin lotuta egon daiteke. Seinale tipikoen artean, hanketako orban gorri edo moreak, ontzi txikien inplikazioa eta kasuen ehuneko 30ean, gorputzeko beste atal batzuk ere kaltetuta daude. Kasu gehienak bere kabuz argitzen dira aste batzuk edo hilabete batzuetara. Tratamendua zein larritasunaren arabera aldatzen da, ahozko kortikoideak pixkanaka murrizten hasi eta esteroideik gabe hantura murrizten duten beste sendagai batzuk erabiltzera.
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.
○ Diagnostikoa
Baskulitis larruazalera mugatzen denean, denborarekin hobetu daiteke. Hala ere, odol‑ eta gernu‑azterketak egin daitezke nahaste sistemikoak edo autoimuneak detektatzeko.
○ Tratamendua ― OTC Drogak
Baskulitis larruazalera mugatzen bada eta beste organoen inbasiorik ez badu, esteroide‑pomada bat erabil daiteke.
#OTC steroid ointment