Vasculitis - Vaskulît
☆ Di encamên 2022-an de Stiftung Warentest ji Almanyayê, razîbûna xerîdar bi ModelDerm tenê ji şêwirmendên telemedicine drav hindik hindiktir bû.
Nexweşiyên din ên pergalî (nexweşiyên otoîmmune) yên ku bi vaskulît re têkildar in, divê bêne derxistin.
Ev wêneyek tîpîk a vasculitis ya lingê ye. Ji bo kontrolkirina anormaliyên di fonksiyona gurçikê de ceribandinek mîzê dikare were kirin.
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 celebek iltîhaba çerm e ku bandorê li damarên xwînê yên piçûk ên di qatên kûr ên çerm de dike. Ew dikare bêyî sedemek naskirî çêbibe an bi enfeksiyonan, tumor, nexweşiyên otoîmmune, an dermanan ve girêdayî be. Nîşanên tîpîk deqên sor an binefşî yên li ser lingan, tevlêbûna keştiyên piçûk, û di ji sedî 30-ê bûyeran de, parçeyên din ên laş jî bandor dibin. Pir bûyer di nav çend hefte û mehan de bi serê xwe paqij dibin. Dermankirin li gorî giraniya wê diguhere, ji kêmkirina hêdî hêdî kortîkosteroîdên devkî bigire heya karanîna dermanên din ên ku iltîhaba bêyî steroîd kêm dike.
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.
○ Teşhîs
Vasculitis bi çermê sînorkirî dibe ku bi demê re baştir bibe. Lêbelê, ceribandinên xwînê û mîzê dikarin bêne kirin da ku nexweşiyên pergalî an otoîmmune bibînin.
○ Dermankirin - Dermanên OTC
Ger vaskulît bêyî ketina organên din bi çerm sînorkirî be, dibe ku rûnê steroîdan were bikar anîn.
#OTC steroid ointment