Skin and Cancer Foundation, Carlton, Victoria, Australia.
Australas J Dermatol. 2011 Feb;52(1):52-5. doi: 10.1111/j.1440-0960.2010.00673.x.
A 28-year-old Costa Rican woman presented with a 6-year history of an asymptomatic progressive localized livedo racemosa on her limbs. Histological examination revealed a lymphocytic vasculitis targeting the arterioles in the deep dermis. In addition, a distinct hyalinised fibrin ring was noted at the periphery of the vessel lumen. These findings were consistent with the recently described entity known as lymphocytic thrombophilic arteritis. An extensive array of investigations did not show any underlying systemic disease, and the patient has remained in good health without treatment.
一位 28 岁的哥斯达黎加女性因四肢无症状性进行性局限性Racemosa 样红斑 6 年来就诊。组织学检查显示真皮深部小动脉淋巴细胞性血管炎。此外,还在血管腔的周边发现了明显的玻璃样纤维蛋白环。这些发现与最近描述的一种称为淋巴细胞血栓性动脉炎的实体一致。广泛的检查未发现任何潜在的系统性疾病,患者在未经治疗的情况下保持良好的健康状态。