Perniciaro C V, Winkelmann R K, Hunder G G
Department of Dermatology, Mayo Clinic, Rochester, MN 55905.
J Am Acad Dermatol. 1987 Dec;17(6):998-1005. doi: 10.1016/s0190-9622(87)70289-8.
Takayasu's arteritis is a chronic, granulomatous, large-vessel arteriopathy of unknown cause. We retrospectively reviewed the medical records of 38 patients with Takayasu's arteritis and identified 21 with cutaneous findings. Seven patients had lesions that were related to their systemic vasculitis. We found a Churg-Strauss granuloma, a pyodermatous leg ulcer, and inflammatory leg nodules in these patients. Biopsy specimens from three patients with presumed "erythema nodosum" did not support the clinical diagnosis but did show arteritis. In patients with Takayasu's arteritis, small-vessel inflammation, and other inflammatory lesions may be present, in addition to large-vessel disease. Histopathologic study is necessary to categorize the nature of inflammatory leg nodules of these patients.
高安动脉炎是一种病因不明的慢性、肉芽肿性大血管动脉病。我们回顾性分析了38例高安动脉炎患者的病历,确定其中21例有皮肤表现。7例患者的皮损与其系统性血管炎相关。我们在这些患者中发现了1例变应性肉芽肿血管炎、1例坏疽性腿部溃疡和炎性腿部结节。3例临床诊断为“结节性红斑”的患者的活检标本不支持临床诊断,但显示有动脉炎。在高安动脉炎患者中,除大血管病变外,还可能存在小血管炎症和其他炎性病变。对这些患者炎性腿部结节的性质进行分类需要进行组织病理学研究。