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10.11604/pamj.2017.26.138.9721

http://scihub22266oqcxt.onion/10.11604/pamj.2017.26.138.9721
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C5429439!5429439!28533861
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suck abstract from ncbi


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pmid28533861      Pan+Afr+Med+J 2017 ; 26 (ä): ä
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  • Vascularites cutanées leucocytoclasiques: à propos de 85 cas #MMPMID28533861
  • Aounallah A; Arouss A; Ghariani N; Saidi W; Sriha B; Denguezli M; Belajouza C; Nouira R
  • Pan Afr Med J 2017[]; 26 (ä): ä PMID28533861show ga
  • Clinical manifestation, etiology and outcome of leukocytoclastic vasculitis are little studied. The aim of our study was to examine epidemiological, clinical etiological, and evolutionary characteristics of this entity. We conducted a cross-sectional data collection from medical records of 85 patients with leukocytoclastic vasculitis in the Department of Dermatology at the Farhat Hached University Hospital, Sousse between January 2000 and December 2013. Epidemiological, clinical, paraclinical, etiological data sheets had been completed for each patient. The average age of patients was 47.65 years, ranging between 10 and 78 years. Fifty-three women and 32 men were registered (sex ratio = 0.6). Cutaneous manifestations were dominated by vascular purpura (88.2%). The most common causes of leukocytoclastic vasculitis were systemic diseases (51%), infection (20%) and neutrophilic dermatoses (14.5%). Other causes were drugs (9.1%) and hematologic malignancies (5.4%). The cause of leukocytoclastic vasculitis was not detected in 30 patients (35, 3%). Two predictive factors associated with the acute outcome were retained: the presence of a recent infection (p= 0.014) and drug intake before the rash (p= 0.013). Chronic evolution was positively correlated with antinuclear antibodies (p= 0.009) and cryoglobulinemia (p=0.025). Our study highlights the multitude of causes of leukocytoclastic vasculitis. The search for an underlying disease is an imperative in order to ensure better therapeutic management.
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