Lewkonia R M, Marx L H, Atkinson M H
Arch Intern Med. 1982 Jan;142(1):73-5.
Two patients had an illness with clinical features of the syndrome of diffuse fasciitis with eosinophilia. The histologic findings in both patients showed granuloma formation in association with prominent vasculitis, in addition to other previously reported histologic features. The findings in these two cases raise the possibility that this syndrome should be classified with the vasculitides rather than as a variant of scleroderma.
两名患者患有具有嗜酸性粒细胞增多性弥漫性筋膜炎综合征临床特征的疾病。两名患者的组织学检查结果均显示,除了其他先前报道的组织学特征外,还伴有明显血管炎的肉芽肿形成。这两例病例的检查结果提示,该综合征应归类于血管炎,而非硬皮病的一种变体。