Vasculitis
☆ I te 2022 Stiftung Warentest hua mai i Tiamana, he iti noa iho te pai o nga kaihoko ki a ModelDerm i nga korero mo te waea rongoa utu.
Ko etahi atu mate kino (mate autoimmune) e pa ana ki te vasculitis me whakakore.
He pikitia angamaheni o te vasculitis o te waewae. Ka taea te mahi he whakamatautau mimi ki te tirotiro mo nga mate o te mahi whatukuhu.
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.
Ko te Leukocytoclastic vasculitis he momo mumura kiri e pa ana ki nga oko toto iti i nga papa hohonu o te kiri. Ka puta mo te kore mohio he take, ka hono ranei ki nga mate, ki nga pukupuku, ki nga mate autoimmune, ki nga rongoa ranei. Ko nga tohu tohu ko nga waahi whero, papura ranei i runga i nga waewae, te urunga o nga oko iti, a, i roto i te 30 paiheneti o nga keehi, ka pangia etahi atu wahanga o te tinana. Ko te nuinga o nga keehi ka maarama ake i roto i etahi wiki ki nga marama. He rereke nga maimoatanga i runga i te kaha o te mate, mai i te whakaheke haere i nga corticosteroids-waha ki te whakamahi i etahi atu raau taero hei whakaheke i te mumura kaore he 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.
○ Tataritanga
Ko te Vasculitis iti ki te kiri ka pai ake i te waa. Heoi ano, ka mahia nga whakamatautau toto me te mimi kia kitea nga mate o te punaha, te mate autoimmune ranei.
○ Maimoatanga - Rongoa OTC
Mēnā ka whāitihia te vasculitis ki te kiri karekau e pangia e ētahi atu whekau, ka taea te whakamahi i te hinu steroid.
#OTC steroid ointment