Open Access Articles- Top Results for Pityriasis rosea

Pityriasis rosea

Pityriasis rosea
Pityriasis rosea on human back and front
Classification and external resources
ICD-10 L42
ICD-9 696.3
DiseasesDB 24698
MedlinePlus 000871
eMedicine derm/335 emerg/426 ped/1815
NCI Pityriasis rosea
Patient UK Pityriasis rosea
MeSH D017515

Pityriasis rosea (also known as pityriasis rosea Gibert[1]) is a skin rash. It is benign but may inflict substantial discomfort in certain cases.[2] Classically, it begins with a single "herald patch" lesion, followed in 1 or 2 weeks by a generalized body rash lasting up to 12 weeks, however usually around 6 - 8.[3][4][5]

Signs and symptoms

Pityriasis rosea on human torso

The symptoms of this condition include:

  • An upper respiratory tract infection may precede all other symptoms in as many as 69% of patients.[6]
  • A single, 2- to (rarely) 10-cm oval red "herald" patch appears, classically on the abdomen.[5][7] Occasionally, the "herald" patch may occur in a 'hidden' position (in the armpit, for example) and not be noticed immediately. The "herald" patch may also appear as a cluster of smaller oval spots, and be mistaken for acne. Rarely, it does not become present at all.[7]
  • 7–14 days after the herald patch, many small (5–10 mm) patches of pink or red, flaky, oval-shaped rash appear on the torso.[7] In 6% of cases an inverse distribution may occur, with rash mostly on the extremities.[8] The more numerous oval patches generally spread widely across the chest first, following the rib-line in a characteristic "christmas-tree" distribution.[7] Small, circular patches may appear on the back and neck several days later. It is unusual for lesions to form on the face, but they may appear on the cheeks or at the hairline.
  • About one in four people with PR suffer from mild to severe symptomatic itching. (Moderate itching due to skin over-dryness is much more common, especially if soap is used to cleanse the affected areas.) The itching is often non-specific, and worsens if scratched. This tends to fade as the rash develops and does not usually last through the entire course of the disease.[7]
  • The rash may be accompanied by low-grade fever, headache, nausea and fatigue. Over-the-counter medications can help manage these.[7]


The cause of pityriasis rosea is not certain, but its clinical presentation and immunologic reactions suggest a viral infection as a cause. Some believe it to be a reactivation of herpes viruses 6 and 7, which cause roseola in infants.[9][10][11][12]


A herald patch of pityriasis rosea which started before the rest of the lesion and was initially mistaken for a fungal infection

Experienced practitioners may make the diagnosis clinically.[5] If the diagnosis is in doubt, tests may be performed to rule out similar conditions such as Lyme disease, ringworm, guttate psoriasis, nummular or discoid eczema, drug eruptions, other viral exanthems.[5][13] A biopsy of the lesions will show extravasated erythrocytes within dermal papillae and dyskeratotic cells within the dermis.[5]

A set of validated diagnostic criteria for pityriasis rosea[14][15] is as follows:

A patient is diagnosed as having pityriasis rosea if:

  1. On at least one occasion or clinical encounter, he / she has all the essential clinical features and at least one of the optional clinical features, and
  2. On all occasions or clinical encounters related to the rash, he / she does not have any of the exclusional clinical features.

The essential clinical features are the following:

  1. Discrete circular or oval lesions,
  2. Scaling on most lesions, and
  3. Peripheral collarette scaling with central clearance on at least two lesions.

The optional clinical features are the following:

  1. Truncal and proximal limb distribution, with less than 10% of lesions distal to mid-upper-arm and mid-thigh,
  2. Orientation of most lesions along skin cleavage lines, and
  3. A herald patch (not necessarily the largest) appearing at least two days before eruption of other lesions, from history of the patient or from clinical observation.

The exclusional clinical features are the following:

  1. Multiple small vesicles at the centre of two or more lesions,
  2. Two or more lesions on palmar or plantar skin surfaces, and
  3. Clinical or serological evidence of secondary syphilis.


No treatment is usually required.

Oral antihistamines or topical steroids may be used to decrease itching.[5] Steroids do provide relief from itching, and improve the appearance of the rash, but they also cause the new skin that forms (after the rash subsides) to take longer to match the surrounding skin color. While no scarring has been found to be associated with the rash, itching and scratching should be avoided. It's possible that scratching can make itching worse and an itch-scratch cycle may develop with regular scratching (that is, you itch more because you scratch, so you scratch more because you itch, and so on). Irritants such as soaps with fragrances, hot water, wool, and synthetic fabrics should be avoided; a soap containing moisturizers (such as goat's milk) may be used, however, and any generic moisturizer can help to manage over-dryness. Calamine lotion may be soothing to the skin and reduce itching. Emulsifiers should be used instead of soaps, as emulsifiers are gentler on the skin and include cleansers, eliminating the need for soap.

Direct sunlight makes the lesions resolve more quickly.[5] According to this principle, medical treatment with ultraviolet light has been used to hasten resolution,[16] though studies disagree whether it decreases itching[16] or not.[17] UV therapy is most beneficial in the first week of the eruption.[16]

Oral erythromycin was effective in treating patients.[18]

Human Herpes Virus 6 or Human Herpes Virus 7 has been hypothesized to be the cause. The antiviral drug Acyclovir can reduce length of duration and severity.[19]


In most patients, the condition lasts only a matter of weeks; in some cases it can last longer (up to six months). The disease resolves completely without long-term effects. Two percent of patients have recurrence.[20][21]


The overall prevalence of PR in the United States has been estimated to be 0.13% in men and 0.14% in women. It most commonly occurs between the ages of 10 and 35.[5] It is more common in spring.[5]

PR is not viewed as contagious,[2][22] though there have been reports of small epidemics in fraternity houses and military bases, schools and gyms.[5]

See also


  1. ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0. 
  2. ^ a b "Pityriasis rosea". American Osteopathic College of Dermatology. Retrieved 26 Jan 2010. 
  3. ^ Freedberg et al. (2003). Fitzpatrick's Dermatology in General Medicine (6th ed.). McGraw-Hill. p. 445. ISBN 0-07-138076-0 
  4. ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology (10th ed.). Saunders. pp. 208–9. ISBN 0-7216-2921-0. 
  5. ^ a b c d e f g h i j Habif, Thomas P (2004). Clinical Dermatology: A Clinical Guide to Diagnosis and Therapy (4th ed.). Mosby. pp. 246–8. ISBN 0-323-01319-8 
  6. ^ Sharma PK, Yadav TP, Gautam RK, Taneja N, Satyanarayana L (2000). "Erythromycin in pityriasis rosea: A double-blind, placebo-controlled clinical trial". J. Am. Acad. Dermatol. 42 (2 Pt 1): 241–244. PMID 10642679. doi:10.1016/S0190-9622(00)90132-4. 
  7. ^ a b c d e f "Pityriasis rosea". American Academy of Dermatology. 2003. Retrieved 2009-06-04. 
  8. ^ Tay YK, Goh CL (1999). "One-year review of pityriasis rosea at the National Skin Centre, Singapore". Ann. Acad. Med. Singap. 28 (6): 829–831. PMID 10672397. 
  9. ^
  10. ^
  11. ^ Medscape > Pityriasis Rosea Author: Robert A Allen, MD; Chief Editor: Dirk M Elston, MD. Updated: Feb 13, 2009
  12. ^ Cynthia M. Magro; A. Neil Crowson; Martin C. Mihm (2007). The Cutaneous Lymphoid Proliferations: A Comprehensive Textbook of Lymphocytic Infiltrates of the Skin. John Wiley and Sons. pp. 36–. ISBN 978-0-471-69598-1. Retrieved 10 November 2010. 
  13. ^ Horn T, Kazakis A (1987). "Pityriasis rosea and the need for a serologic test for syphilis". Cutis 39 (1): 81–2. PMID 3802914. 
  14. ^ Chuh AA (2003). "Diagnostic criteria for pityriasis rosea: a prospective case control study for assessment of validity". J Eur Acad Dermatol Venereol 17 (1): 101–3. PMID 12602987. doi:10.1046/j.1468-3083.2003.00519_4.x. 
  15. ^ Chuh A, Zawar V, Law M, Sciallis G (2012). "Gianotti-Crosti syndrome, pityriasis rosea, asymmetrical periflexural exanthem, unilateral mediothoracic exanthem, eruptive pseudoangiomatosis, and papular-purpuric gloves and socks syndrome: a brief review and arguments for diagnostic criteria". Infect Dis Rep 4 (1): e12. PMC 3892651. PMID 24470919. doi:10.4081/idr.2012.e12. 
  16. ^ a b c Arndt KA, Paul BS, Stern RS, Parrish JA (1983). "Treatment of pityriasis rosea with UV radiation". Arch Dermatol 119 (5): 381–2. PMID 6847217. doi:10.1001/archderm.119.5.381. 
  17. ^ Leenutaphong V, Jiamton S (1995). "UVB phototherapy for pityriasis rosea: a bilateral compatison study". J Am Acad Dermatol 33 (6): 996–9. PMID 7490372. doi:10.1016/0190-9622(95)90293-7. 
  18. ^ Sharma, P.K. (2000). "Erythromycin in pityriasis rosea: A double-blind, placebo-controlled clinical trial". J.Am.Acad.Dermatol. 42 (2): 241–244. doi:10.1016/s0190-9622(00)90132-4. 
  19. ^ Ganguly S (2014). "A Randomized, Double-blind, Placebo-Controlled Study of Efficacy of Oral Acyclovir in the Treatment of Pityriasis Rosea". J Clin Diagn Res 8 (5): YC01–YC04. PMID 24995231. doi:10.7860/JCDR/2014/8140.4360. 
  20. ^ Kempf W, Adams V, Kleinhans M, Burg G, Panizzon RG, Campadelli-Fiume G et al. (1999). "Pityriasis rosea is not associated with human herpesvirus 7". Arch Dermatol 135 (9): 1070–2. PMID 10490111. doi:10.1001/archderm.135.9.1070. 
  21. ^ Chuang TY, Ilstrup DM, Perry HO, Kurland LT (1982). "Pityriasis rosea in Rochester, Minnesota, 1969 to 1978". J. Am. Acad. Dermatol. 7 (1): 80–9. PMID 6980904. doi:10.1016/s0190-9622(82)80013-3. 
  22. ^ "Pityriasis rosea". Retrieved 26 Jan 2010. 

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