ተጨማሪ መረጃ ― አማርኛ

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 በቆዳው ጥልቅ ንብርብቶች ውስጥ የሚገኙ ትናንሽ የደም ቧንቧዎችን የሚያጠቃ የቆዳ እብጠት አይነት ነው። በማይታወቅ ምክንያት ሊከሰት ወይም ከኢንፌክሽን፣ እጢዎች፣ ራስን በራስ የሚከላከሉ በሽታዎች ወይም መድሃኒቶች ጋር ሊገናኝ ይችላል። ከተለመዱት ምልክቶች መካከል በእግሮቹ ላይ ቀይ ወይም ወይን ጠጅ ነጠብጣቦች ፣ የትናንሽ መርከቦች ተሳትፎ ፣ እና በ 30 በመቶ ከሚሆኑ ጉዳዮች ፣ ሌሎች የሰውነት ክፍሎችም ይጎዳሉ። ብዙ ጉዳዮች ከጥቂት ሳምንታት እስከ ወራቶች ውስጥ በራሳቸው ይጠፋሉ. ሕክምናው ምን ያህል ከባድ እንደሆነ ይለያያል፣ የአፍ ውስጥ ኮርቲሲቶይድን ቀስ በቀስ ከመቀነስ ጀምሮ ያለ ስቴሮይድ እብጠትን የሚቀንሱ ሌሎች መድኃኒቶችን መጠቀም።
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.