Atypical pityriasis Rubra Pilaris associated with arthropathy and osteoporosis: A case report with 15-year follow-up

被引：10

作者：

Behr, FD ^{[1
]}

Bangert, JL ^{[1
]}

Hansen, RC ^{[1
]}

机构：

[1] Univ Arizona, Coll Med, Dermatol Sect, Tucson, AZ 85721 USA

来源：

PEDIATRIC DERMATOLOGY | 2002年 / 19卷 / 01期

关键词：

D O I：

10.1046/j.1525-1470.2002.00004.x

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 an idiopathic papulosquamous disease that clinically presents with palmoplantar keratoderma and follicular hyperkeratotic papules that coalesce into scaly erythematous plaques. We report a unique case of atypical PRP beginning at 1 year of age with associated severe arthropathy and osteoporosis. We further discuss the clinical and histopathologic aspects of PRP, its possible etiology, and other associated conditions.

引用

页码：46 / 51

页数：6

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