Literature DB >> 16403386

Pityriasis rubra pilaris, type IV.

Jennifer Bragg1, Agnieszka Witkiewicz, Seth J Orlow, Julie V Schaffer.   

Abstract

A 4-year-old girl presented with a 3-year history of demarcated, salmon-pink, hyperkeratotic plaques, which were symmetrically distributed on the elbows, knees, ankles, and dorsal aspects of the hands and feet. A diffuse, orange-pink palmoplantar keratoderma was also evident. Clinical and histologic findings were consistent with a diagnosis of pityriasis rubra pilaris (PRP), type IV (circumscribed juvenile). Type IV PRP develops in prepubertal children, is typically localized to the distal aspects of the extremities, and has an unpredictable course. Although ultraviolet (UV) radiation can potentially exacerbate PRP, our patient has improved with broad-band UVB phototherapy.

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Year:  2005        PMID: 16403386

Source DB:  PubMed          Journal:  Dermatol Online J        ISSN: 1087-2108


  3 in total

1.  An unusual rash.

Authors:  Dominic Muogbo; David Cremonesini
Journal:  BMJ Case Rep       Date:  2010-05-19

2.  Ineffectiveness of tumor necrosis factor-α blockers and ustekinumab in a case of type IV pityriasis rubra pilaris.

Authors:  Vito Di Lernia; Elena Ficarelli; Magda Zanelli
Journal:  Indian Dermatol Online J       Date:  2015 May-Jun

Review 3.  Management of refractory pityriasis rubra pilaris: challenges and solutions.

Authors:  Gaia Moretta; Erika V De Luca; Alessandro Di Stefani
Journal:  Clin Cosmet Investig Dermatol       Date:  2017-11-09
  3 in total

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