Vasculitis
https://en.wikipedia.org/wiki/Vasculitis
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Purpura

Henoch schonlein purpura
relevance score : -100.0%
References
An aetiological & clinicopathological study on cutaneous vasculitis 22382191 NIH
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 29489227 NIH
Leukocytoclastic vasculitis ndi mtundu wa kutupa pakhungu komwe kumakhudza timitsempha ting'onoting'ono m'kati mwa khungu. Zitha kuchitika popanda chifukwa chodziwika kapena kulumikizidwa ndi matenda, zotupa, matenda a autoimmune, kapena mankhwala. Zizindikiro zodziwika bwino ndi monga mawanga ofiira kapena ofiirira m'miyendo, kugunda kwa timitsempha tating'onoting'ono, ndipo pafupifupi 30 peresenti ya milandu, mbali zina zathupi nazonso zimakhudzidwa. Milandu yambiri imatha paokha pakatha milungu ingapo mpaka miyezi ingapo. Chithandizo chimasiyanasiyana malinga ndi momwe zimakhalira, kuyambira pang'onopang'ono kuchepetsa oral corticosteroids mpaka kugwiritsa ntchito mankhwala ena omwe amachepetsa kutupa popanda 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.
○ Matenda
Vasculitis yokha pakhungu imatha kusintha pakapita nthawi. Komabe, kuyezetsa magazi ndi mkodzo kumatha kuchitidwa kuti azindikire zovuta za systemic kapena autoimmune.
○ Kuchiza - Mankhwala OTC
Ngati vasculitis imangokhala pakhungu popanda kuukira ziwalo zina, mafuta a steroid angagwiritsidwe ntchito.
#OTC steroid ointment