Aounallah Amina, Arouss Aicha, Ghariani Najet, Saidi Wafa, Sriha Badreddine, Denguezli Mohamed, Belajouza Colandane, Nouira Rafia
Université du Centre, Tunisie.
Service de Dermatologie, CHU Farhat Hached, Sousse, Tunisie.
Pan Afr Med J. 2017 Mar 14;26:138. doi: 10.11604/pamj.2017.26.138.9721. eCollection 2017.
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.
白细胞破碎性血管炎的临床表现、病因及预后鲜少被研究。我们研究的目的是探究该疾病的流行病学、临床病因及演变特征。我们对2000年1月至2013年12月期间苏塞法哈特·哈谢德大学医院皮肤科85例白细胞破碎性血管炎患者的病历进行了横断面数据收集。为每位患者填写了流行病学、临床、辅助检查、病因数据表。患者的平均年龄为47.65岁,年龄范围在10岁至78岁之间。登记的患者中有53名女性和32名男性(性别比=0.6)。皮肤表现以血管性紫癜为主(88.2%)。白细胞破碎性血管炎最常见的病因是全身性疾病(51%)、感染(20%)和嗜中性皮病(14.5%)。其他病因包括药物(9.1%)和血液系统恶性肿瘤(5.4%)。30例患者(35.3%)未检测到白细胞破碎性血管炎的病因。与急性预后相关的两个预测因素被确定:近期感染的存在(p=0.014)和出疹前的药物摄入(p=0.013)。慢性演变与抗核抗体(p=0.009)和冷球蛋白血症(p=0.025)呈正相关。我们的研究强调了白细胞破碎性血管炎病因的多样性。寻找潜在疾病对于确保更好的治疗管理至关重要。