| Literature DB >> 11860571 |
Fiona D Behr1, Jerry L Bangert, Ronald C Hansen.
Abstract
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.Entities:
Mesh：
Year: 2002 PMID： 11860571 DOI： 10.1046/j.1525-1470.2002.00004.x
Source DB: PubMed Journal: Pediatr Dermatol ISSN： 0736-8046 Impact factor: 1.588