Lowes M A, Khaira G S, Holt D
Dermatology Department, Royal Newcastle Hospital, Australia.
Australas J Dermatol. 2000 Aug;41(3):172-4. doi: 10.1046/j.1440-0960.2000.00424.x.
A 20-year-old female with cystic fibrosis presented with a white marginal palmar eruption after exposure to water. There was no family history of keratoderma. A biopsy showed hyperkeratosis around dilated eccrine ostia. These features are similar to a recently described condition, transient reactive papulotranslucent acrokeratoderma. This is thought to be a variant of hereditary papulotranslucent acrokeratoderma, one of the punctate keratodermas. Association with cystic fibrosis has not been described previously.
一名20岁患有囊性纤维化的女性在接触水后出现手掌边缘白色皮疹。无掌跖角化病家族史。活检显示扩张的小汗腺开口周围有角化过度。这些特征与最近描述的一种疾病——短暂性反应性丘疹半透明肢端角化病相似。这被认为是遗传性丘疹半透明肢端角化病（点状角化病之一）的一种变体。此前尚未描述过与囊性纤维化的关联。
