Vasculitis - Vaskulit
☆ Nan rezilta Stiftung Warentest 2022 ki soti nan Almay, satisfaksyon konsomatè yo ak ModelDerm te sèlman yon ti kras pi ba pase ak konsiltasyon telemedsin peye.
Yo ta dwe elimine lòt maladi sistemik (maladi otoiminitè) ki enplike vaskulit.
Sa a se yon foto tipik nan vaskulit nan janm la. Yo ka fè yon tès pipi pou tcheke si gen anòmal nan fonksyon ren yo.
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 se yon kalite enflamasyon po ki afekte ti veso sangen nan kouch pwofon po a. Li ka rive san okenn rezon konnen oswa li ka lye ak enfeksyon, timè, maladi otoiminitè, oswa medikaman. Siy tipik yo enkli tach wouj oswa koulè wouj violèt sou janm yo, patisipasyon nan ti veso, ak nan apeprè 30 pousan nan ka yo, lòt pati nan kò a afekte tou. Pifò ka klè poukont yo nan kèk semèn a mwa. Tretman varye selon ki jan grav li ye, soti nan diminye piti piti kortikoterapi oral yo sèvi ak lòt dwòg ki diminye enflamasyon san estewoyid.
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.
○ Dyagnostik
Vaskulit limite a po a ka amelyore sou tan. Sepandan, tès san ak pipi yo ka fè pou detekte maladi sistemik oswa otoiminitè.
○ Tretman - Medikaman OTC
Si vaskulit limite a po a san yo pa envazyon lòt ògàn yo, yo ka itilize yon odè esteroyid.
#OTC steroid ointment