Nousari H C, Kimyai-Asadi A, Stone J H
Department of Dermatology, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
J Am Acad Dermatol. 2000 Nov;43(5 Pt 2):955-7. doi: 10.1067/mjd.2000.103643.
Leukocytoclastic vasculitis is a condition characterized by necrotizing neutrophilic inflammation of small dermal blood vessels usually resulting in palpable purpuric lesions. Leukocytoclastic vasculitis may be secondary to a variety of medications and underlying disease processes, including infections, connective tissue disorders, and malignancies. We describe a patient with a monoclonal gammopathy of unknown significance in whom leukocytoclastic vasculitis developed, manifested by a few prominent annular plaques on the lower extremity. The rare association between monoclonal gammopathy of unknown significance and leukocytoclastic vasculitis as well as the unusual annular presentation of the disease in this patient is discussed, and the relevant literature is reviewed.
白细胞破碎性血管炎是一种以真皮小血管坏死性中性粒细胞炎症为特征的疾病,通常导致可触及的紫癜性病变。白细胞破碎性血管炎可能继发于多种药物和潜在疾病过程,包括感染、结缔组织疾病和恶性肿瘤。我们描述了一名意义未明的单克隆丙种球蛋白病患者,该患者发生了白细胞破碎性血管炎,表现为下肢有几个突出的环形斑块。讨论了意义未明的单克隆丙种球蛋白病与白细胞破碎性血管炎之间的罕见关联以及该疾病在该患者中不寻常的环形表现,并对相关文献进行了综述。