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Pityriasis Rosea

Pityriasis rosea is an acute, self-limiting skin condition. A primary plaque ('herald patch') is followed by a distinctive, generalized itchy rash 1-2 weeks later. The rash lasts for approximately 2-6 weeks. Lesions are typically oval, dull pink or tawny and appear in a 'Christmas tree' distribution, usually on the trunk and the upper arms and legs.1

Epidemiology
  • The overall prevalence is approximately 0.15%.2
  • Pityriasis rosea is most common in children and young adults, with 15-40 years being the peak age range affected. Pityriasis rosea is rare in infants and in the elderly.
  • Occurs most often during the spring and autumn.
  • Some drugs, e.g. bismuth, barbiturates, captopril, gold, metronidazole, D-penicillamine and isotretinoin, occasionally cause a drug-induced pityriasis rosea.
Presentation

PITYRIASIS ROSEA -ON ABDOMEN (DIS81.jpg)

  • There may be prodromal symptoms, e.g. malaise, nausea, anorexia, fever, joint pain, lymph node swelling, headache, that precede the appearance of the herald patch.
  • Pruritus (may be intense) occurs in the majority of patients.
  • The herald patch measures 1-2 cm in diameter and is oval or round with a central, wrinkled, salmon-coloured area, separated from a dark red peripheral zone by fine scales. The herald patch is usually located on the trunk but may be seen on the neck or extremities.
  • The secondary rash is symmetrical and localized, predominantly to the trunk, neck and proximal extremities.
  • The lesions of the secondary rash are small versions of the herald patch, with the two red zones separated by a scaling ring. They are distributed in a Christmas tree pattern.
  • In a minority of patients, the herald patch is either absent confluent with the other lesions.
  • Variant presentations include peripheral distribution of the rash, and facial involvement may be seen in children. Skin lesions may also be large, urticarial, vesicular, pustular, purpuric, and resemble erythema multiforme.
  • Hypopigmentation and hyperpigmentation of affected skin may follow the inflammatory stage. Hyperpigmentation is more common In patients with black skin.
  • Oral lesions are rare but may occur, e.g. erythematous plaques and ulcers.
Investigations
  • Diagnosis is clinical and usually no investigations are required.
  • Skin biopsy may be required to confirm or alter the diagnosis.
  • Other investigations, e.g. syphilis serology, may be required to rule out other possible diagnoses.
Management
  • Pityriasis rosea is a self-limiting disease, and treatment is supportive.
  • Exposure to sunlight is helpful.
  • Topical zinc oxide and calamine lotion are useful for pruritus.
  • Pruritus can be treated with topical corticosteroids, oral antihistamines or antipruritic lotions.
Prognosis
  • It usually lasts for 6-8 weeks before clearing spontaneously.
  • Fewer than 3% of affected individuals experience recurrences.


Document References
  1. Colour Atlas and Synopsis of Clinical Dermatology. Fitzpatrick TB et al. McGraw-Hill 2001.
  2. Lichenstein R; Pityriasis Rosea. eMedicine, June 2006.

Internet and Further Reading Acknowledgements EMIS is grateful to Dr Colin Tidy for writing this article. The final copy has passed scrutiny by the independent Mentor GP reviewing team. ©EMIS 2007.
DocID: 2617
Document Version: 20
DocRef: bgp1033
Last Updated: 8 Mar 2007
Review Date: 7 Mar 2009


















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