Batafsil ma'lumot ― O'zbekcha

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 - terining chuqur qatlamlaridagi mayda qon tomirlariga ta'sir qiluvchi teri yallig'lanishining bir turi. Bu hech qanday sababsiz sodir bo'lishi yoki infektsiyalar, o'smalar, otoimmün kasalliklar yoki dorilar bilan bog'liq bo'lishi mumkin. Odatiy belgilarga oyoqlarda qizil yoki binafsha rangli dog'lar, kichik tomirlarni jalb qilish kiradi va taxminan 30 foiz hollarda tananing boshqa qismlari ham ta'sir qiladi. Aksariyat holatlar bir necha haftadan bir necha oygacha o'z-o'zidan yo'qoladi. Davolash og'iz kortikosteroidlarini asta-sekin kamaytirishdan steroidlarsiz yallig'lanishni kamaytiradigan boshqa dorilarni qo'llashgacha bo'lgan og'irligiga qarab o'zgaradi.
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.