Haneke E, Schwarzenbach I, Hornstein O P
Z Hautkr. 1977 Mar 1;52(5):170-2.
Acrokeratoelastoidosis, first described in 1952 bei O.G. Costa, belongs to the group of diffuse palmoplantar keratoses without associated symptoms. Probably it is an autosomal dominant trait. We observed a 49 year old female who has noticed her typical skin lesions for 2 years. The most marked histological features are proliferative hyperkeratosis, an almost complete lack of the fine subepithelial elastic fibre network and a marked rarefication of the coarse elastic fibres in the dermis.
肢端角化性弹性组织变性于1952年由O.G. 科斯塔首次描述,属于无相关症状的弥漫性掌跖角化病组。它可能是一种常染色体显性性状。我们观察了一名49岁女性,她发现自己典型的皮肤病变已有2年。最显著的组织学特征是增殖性角化过度、上皮下细弹性纤维网络几乎完全缺失以及真皮中粗弹性纤维明显稀疏。