- Pityriasis rubra pilaris
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Pityriasis rubra pilaris Classification and external resources ICD-10 L44.0 ICD-9 696.4 OMIM 173200 DiseasesDB 29305 MedlinePlus 001471 eMedicine derm/337 MeSH D010916 Pityriasis rubra pilaris (also known as "Devergie's disease,"[1] "Lichen ruber acuminatus,"[1] and "Lichen ruber pilaris"[1]) refers to a group of chronic disorders characterized by reddish orange, scaling plaques and keratotic follicular papules.[2]:442 Symptoms may include reddish-orange patches (Latin: rubra) on the skin, severe flaking (Latin: pityriasis), uncomfortable itching, thickening of the skin on the feet and hands, and thickened bumps around hair follicles (Latin: pilus for hair). For some, early symptoms may also include generalized swelling of the legs, feet and other parts of the body. PRP has a varied clinical progression and a varied rate of improvement. There is no known cause or cure.[citation needed]
It was first described by Marie-Guillaume-Alphonse Devergie in 1856,[3] and the condition is also known as Devergie's disease.[4]
Contents
Classification
Dr. W.A.D. Griffiths, from Great Britain, classified six forms of PRP in the early 1980s.[5] At this time, the causes of PRP are still unknown and symptoms can be difficult to diagnose. Frequently, more than one medical professional will be consulted before an accurate PRP diagnosis is made.[citation needed]
Dermatologists have identified both an acquired form and an inherited form (familial) of PRP and have described them in medical journals. The acquired form usually shows a spontaneous or gradual remission of symptoms within several years although long-term symptoms may continue for years. The inherited form starts early in childhood with persistent long-term symptoms into adulthood.[citation needed]
Although most people who develop PRP are over age 50, individuals of any age, race, and nationality can be affected. Women and men seem to be equally affected.[citation needed]
See also
- List of cutaneous conditions
- American Osteopathic Dermatology content: http://www.aocd.org/skin/dermatologic_diseases/pityriasis_rubra_p.html
Footnotes
- ^ a b c Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
- ^ Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0071380760.
- ^ Devergie M. G. A. (1856). "[Pityriasis pilaris, a skin disease not described by dermatologists] (Pityriasis pilaris, maladie de la peau non décrite par les dermatologistes)." (in French). Gazette hebdomadaire de médecine et de chirurgie, Paris 3: 197–201.
- ^ M. G. A. Devergie and the eponymous named Devergie's disease at Who Named It?
- ^ "Pityriasis rubra pilaris". DermNZ (New Zealand Dermatological Society). 26 December 2006. http://dermnetnz.org/scaly/pityriasis-rubra-pilaris.html. Retrieved 2007-05-08. - describes the various forms
External links
- PRP Support Group - information regarding day-to-day care and medical treatment and having an international membership.
- skin diseases Information
- Dr. Griffith (June 1998). "Pityriasis rubra pilaris". In Editors Champion R.H., Burton J.L., Burns D.A. and Breathnach S.M.. Textbook of Dermatology. 2 (6th ed.). pp. 1539–1545. ISBN 0632050640.
Papulosquamous disorders (L40–L45, 696–697) Psoriasis PustularGeneralized pustular psoriasis (Impetigo herpetiformis) · Acropustulosis/Pustulosis palmaris et plantaris (Pustular bacterid) · Annular pustular psoriasis · Localized pustular psoriasisOtherParapsoriasis Pityriasis lichenoides (Pityriasis lichenoides et varioliformis acuta, Pityriasis lichenoides chronica) · Lymphomatoid papulosis · Small plaque parapsoriasis (Digitate dermatosis, Xanthoerythrodermia perstans) · Large plaque parapsoriasis (Retiform parapsoriasis)Other pityriasis Other lichenoid configuration: Annular lichen planus · Linear lichen planus
morphology of lesion: Hypertrophic lichen planus · Atrophic lichen planus · Bullous lichen planus · Ulcerative lichen planus · Lichen planus actinicus · Lichen planus pigmentosus
site of involvement: Mucosal lichen planus · Lichen planus of the nails · Peno-gingival syndrome · Vulvovaginal gingival syndromeoverlap: Lichen planus–lichen sclerosus overlap syndrome · Lichen planus–lupus erythematosus overlap syndrome
special forms: Hepatitis-associated lichen planus · Lichen planus pemphigoidesOtherungrouped lichenoid eruptions: Erythema dyschromicum perstans · Idiopathic eruptive macular pigmentation · Keratosis lichenoides chronica · Kraurosis vulvae · Lichen sclerosus · Lichenoid dermatitis · Lichenoid reaction of graft-versus-host diseaseCategories:- Papulosquamous hyperkeratotic cutaneous conditions
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