Lupton G P, Goette D K
Arch Dermatol. 1979 Jan;115(1):85-7.
Two patients developed an erythematous, rock-hard induration of their forearms after strenuous physical activity. Peripheral eosinophilia was noted in one patient, but hypergammaglobulinemia was absent. Systemic corticosteroid treatment resulted in remarkable involution of the process in one patient, while the other experienced spontaneous involution. The histologic changes were those of eosinophilic fasciitis.
两名患者在剧烈体力活动后前臂出现红斑、质地坚硬如石的硬结。其中一名患者外周血嗜酸性粒细胞增多，但无高球蛋白血症。全身用皮质类固醇治疗使一名患者的病情显著消退，而另一名患者则自行消退。组织学改变符合嗜酸性筋膜炎。
