Lillie M A, Yang L C, Honig P J, August C S
Arch Dermatol. 1983 May;119(5):415-8.
Erythroderma and exfoliative dermatitis developed in a 17-year-old boy following therapy with phenytoin sodium. Immunologic studies performed early in the course of the dermatitis disclosed panhypogammaglobulinemia and a marked increase in T lymphocytes that responded poorly in vitro to T-cell mitogens. After therapy with prednisone, the dermatitis improved somewhat, and the patient's lymphocytes proliferated in vitro when exposed to phenytoin. We speculate that our patient's acute hypersensitivity reaction may have been mediated by an excessive number of phenytoin-sensitized suppressor-cytotoxic T lymphocytes and may represent a disorder of immunoregulatory T cells.
一名17岁男孩在接受苯妥英钠治疗后发生了红皮病和剥脱性皮炎。在皮炎病程早期进行的免疫学研究显示全血细胞减少和T淋巴细胞显著增加,这些T淋巴细胞在体外对T细胞有丝分裂原反应不佳。使用泼尼松治疗后,皮炎有所改善,并且当患者的淋巴细胞暴露于苯妥英时在体外发生增殖。我们推测,我们患者的急性超敏反应可能是由过量的苯妥英致敏抑制性细胞毒性T淋巴细胞介导的,可能代表免疫调节性T细胞的一种疾病。