Pityriasis rubra pilaris

被引：0

作者：

Artik, S ^{[1
]}

Kuhn, A ^{[1
]}

Neumann, NJ ^{[1
]}

Ruzicka, T ^{[1
]}

Megahed, M ^{[1
]}

机构：

[1] Univ Dusseldorf, Hauklin, D-40225 Dusseldorf, Germany

来源：

HAUTARZT | 2004年 / 55卷 / 10期

关键词：

Pityriasis rubra pilaris; generalized erythroderma; acitretin; phototherapy; systemic glucocorticosteroids;

D O I：

10.1007/s00105-004-0811-7

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

Pityriasis rubra pilaris (PRP) is a rare papulosquamous disease with typical onset during the first and fifth decades. The skin disorder normally starts on the scalp and spreads caudally within a few weeks. It often results in a generalized erythroderma with sharply demarcated islands of sparing ("nappes claires"). A 65-year-old patient with severe PRP showed good clinical improvement after 8 months of treatment when treated with acitretin in combination with phototherapy and systemic glucocorticosteroids.

引用

页码：980 / 983

页数：4

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