Mevorah B, Salomon D, Siegenthaler G, Hohl D, Meier M L, Saurat J H, Frenk E
Department of Dermatology, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
J Am Acad Dermatol. 1996 Feb;34(2 Pt 2):379-85. doi: 10.1016/s0190-9622(07)80013-2.
We describe a man with generalized congenital ichthyosiform dermatosis, severe cheilitis, and palmar and plantar hyperkeratosis with superficial blistering. Low-dose acitretin therapy induced areas of peeling skin, similar to that seen in the peeling skin syndrome. Histologically, the skin was moderately hyperkeratotic and the palmar blisters were subcorneal. Electron microscopy revealed that the splitting occurred within the desmosomal plaque. Ultrastructural and biochemical investigations indicated epidermal hypervitaminosis A, probably related to alteration of epidermal retinoic acid metabolism. This disease is proposed as a hitherto unreported variant of the peeling skin syndrome.
我们描述了一名患有全身性先天性鱼鳞病样皮肤病、严重唇炎以及伴有浅表水疱的掌跖角化过度症的男性患者。低剂量阿维A治疗诱发了皮肤脱屑区域,类似于皮肤剥脱综合征所见。组织学上,皮肤呈中度角化过度,掌部水疱位于角质层下。电子显微镜检查显示分裂发生在桥粒斑内。超微结构和生化研究表明存在表皮维生素A过多症,可能与表皮维甲酸代谢改变有关。这种疾病被认为是皮肤剥脱综合征一种迄今未报道的变体。