首页> 美国卫生研究院文献>Anais Brasileiros de Dermatologia >Cutaneous lesions and finger clubbing uncovering hypocomplementemicurticarial vasculitis and hepatitis C with mixed cryoglobulinemia
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Cutaneous lesions and finger clubbing uncovering hypocomplementemicurticarial vasculitis and hepatitis C with mixed cryoglobulinemia

机译:皮损和手指棍棒发现补体不足荨麻疹性血管炎和丙型肝炎合并冷球蛋白血症

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摘要

Urticarial vasculitis is a rare clinicopathologic entity characterized by urticarial lesions that persist for more than 24 hours and histologic features of leukocytoclastic vasculitis. Patients can be divided into normocomplementemic or hypocomplementemic. The authors report the case of a healthy 49-year-old woman with a 1-year history of highly pruritic generalized cutaneous lesions and finger clubbing. Laboratory tests together with histopathologic examination allowed the diagnosis of hypocomplementemic urticarial vasculitis, chronic hepatitis C and type II mixed cryoglobulinemia. The patient started symptomatic treatment and was referred to a gastroenterologist for management of the hepatitis C, with progressive improvement of the skin condition. The development of hypocomplementemic urticarial vasculitis in the context of chronic hepatitis C is exceedingly rare and possible pathogenic mechanisms are discussed.
机译:荨麻疹性血管炎是一种罕见的临床病理学实体,其特征是荨麻疹病变持续超过24小时,并且具有白细胞碎裂性血管炎的组织学特征。患者可分为正常互补性或低互补性。作者报告了一个健康的49岁女性的病例,该女性有1年的高度瘙痒性全身性皮肤病变和手指棍打的病史。实验室检查和组织病理学检查可以诊断为低补体性荨麻疹性血管炎,慢性丙型肝炎和II型混合性冷球蛋白血症。患者开始对症治疗,并转诊为胃肠病专家以治疗丙型肝炎,并逐渐改善皮肤状况。在慢性丙型肝炎的情况下,低补体性荨麻疹性血管炎的发展极为罕见,并探讨了可能的致病机制。

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