Gamborg Nielsen P
Acta Derm Venereol. 1985;65(3):224-9.
A papular and a diffuse variety of hereditary palmoplantar keratoderma (Unna Thost) are described. It was not possible to demonstrate any histopathological differences between the two varieties. Of the patients examined 36.2% were found to have dermatophytosis in addition to hereditary palmoplantar keratoderma. The hyperkeratosis was smooth and uniform in both varieties. When scaling and fissuring did occur they were signs of dermatophytosis and not part of the clinical picture. The examination of biopsies stained with H&E and PAS showed that dermatophytosis in patients with hereditary palmoplantar keratoderma, especially those with recurrent vesicular eruptions, gave rise to a histopathological picture which was, in some respects, similar to that of acute vesicular eczema.
描述了丘疹型和弥漫型遗传性掌跖角化病(乌纳 - 托斯特型)。无法证明这两种类型之间存在任何组织病理学差异。在接受检查的患者中,发现36.2%除了患有遗传性掌跖角化病外还患有皮肤癣菌病。两种类型的角化过度均光滑且均匀。当出现鳞屑和裂隙时,它们是皮肤癣菌病的体征,而非临床表现的一部分。对苏木精 - 伊红染色和过碘酸 - 雪夫染色的活检组织检查显示,遗传性掌跖角化病患者,尤其是那些有复发性水疱疹的患者,其皮肤癣菌病会产生一种在某些方面类似于急性水疱性湿疹的组织病理学表现。