Thyresson H N, Doyle J A, Winkelmann R K
Acta Derm Venereol. 1980;60(3):261-3.
Eighteen cases of granuloma annulare were classified histopathologically and examined by direct immunofluorescence. The three different histopathologic types of granuloma annulare were compared with the result of immunofluorescence examination. No features of leukocytoclastic vasculitis were seen. Direct immunofluorescence of granuloma annulare does not reveal any consistent diagnostic pattern. Dermal desposition of fibrin in necrobiotic areas were noted in 8 cases of 18. Blood vessel and/or basement membrane deposition of IgM and C3 was inconsistent and does not support an immune complex vasculitis. Direct immunofluorescence is useful in studying the pathogenesis of granuloma annulare. The finding of fibrin, together with the histology, suggests to us a delayed hypersensitivity reaction as the dominant pathogenic event.
对18例环状肉芽肿进行了组织病理学分类,并通过直接免疫荧光检查。将环状肉芽肿的三种不同组织病理学类型与免疫荧光检查结果进行了比较。未发现白细胞破碎性血管炎的特征。环状肉芽肿的直接免疫荧光未显示任何一致的诊断模式。18例中有8例在坏死区域发现纤维蛋白的真皮沉积。IgM和C3在血管和/或基底膜的沉积不一致,不支持免疫复合物性血管炎。直接免疫荧光有助于研究环状肉芽肿的发病机制。纤维蛋白的发现,结合组织学,提示我们迟发型超敏反应是主要的致病事件。