1.5.5 Pityriasis Rosea

Grading & Level of Importance: B
Review:
2026

W. Burgdorf, Munich; A. Salam, J. McGrath, London
Revised by C.C. Zouboulis, Dessau; H. Gollnick, Magdeburg

ICD-11

 EA10

Synonyms

Pityriasis circinata; Gibert pityriasis; Pityriasis rosea Gibert. 

Epidemiology

Common disease (incidence 0.68/100 dermatology patients, prevalence 0.5-2%). Affects adolescents and young adults (aged 10 to 35 years). 

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It affects adolescents and young adults (aged 10 to 35 years). Incidence is 0.68/100 dermatology patients, prevalence 0.5-2% with a peak incidence in spring and autumn.

Definition

Acute, disseminated, symmetrical exanthem with collarette scale.

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Acute, disseminated, self-limiting symmetrical papulo-squamous exanthem with typical collarette scale.

Aetiology & Pathogenesis

Probably viral induction (human herpes virus 6 or 7).

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The disease was first described by Gibert in 1860. The etiology of PR remains largely uncertain, with hypotheses directed towards either infectious HHV and others or non-infectious origins (post vaccination) or both. It probably arises as an “id”- reaction to some viral infections (human herpes virus 6 in adolescence or 7 in adults (HHV6/7). Thereafter long-life immunity exists. In HIV immunocompromised patients it can be seen more often and was reported during the corona epidemic quite more often, but more a pattern which was pityriasis rosea-like. There is also evidence that dermatologists are more often affected than other members of medical disciplines.

Signs & Symptoms

The initial lesion is a large, flat erythematous (salmon coloured) plaque (herald patch (medallion), up to 5 cm in diameter), followed by multiple smaller lesions frequently following skin lines (e.g. Christmas tree distribution around ribs) with a typical collarette scale. Similar long axis orientation for individual plaque. Pruritus can occur (50%) and is variable in intensity, especially when skin is irritated by intense washing, sweating, or with simultaneous concurrent dermatitis. Prodromal symptoms (fever, headache, arthralgia, cough, vomiting, or lymphadenopathy) have been reported up to 60% of the patients.

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The initial lesion is a large erythematous (salmon coloured) patch (herald patch, medallion, tâche- mère), up to 5 cm in diameter), followed by multiple smaller lesions frequently following skin lines (e.g. Christmas tree distribution around ribs) being thin with a typical collarette scale. Similar long axis orientation for individual patches.

Pruritus can occur (50%) and is variable in intensity, especially when skin is irritated (intense washing, drying medications or with simultaneous concurrent dermatitis). In children sometimes a so-called inverse form can occur and manifests in the axillae and the groin region.

Post-inflammatory hypopigmentation or hyperpigmentation (lighter or darker patches of skin) can occur.

Prodromal symptoms (fever, headache, arthralgia, cough, vomiting, or lymphadenopathy) have been reported in 60% of the patients.

Localisation

Typically, on trunk (occasionally neck and proximal extremities).

Classification

Atypical variants can occur. 

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Common disease. Up to 20% atypical clinical variants can occur, more often in children.

Laboratory & other workups

Not necessary. 

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Not required, but syphilis should be ruled in adults.

Dermatopathology

Not required. Corresponds to eczematous dermatitis; patchy lymphocytic infiltrate in the dermis and a few intraepidermal erythrocytes. 

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Primarily not required. In case of unusual course or atypical pattern. No specific pattern with edema in the stratum papillary, mild epidermal spongiosis and some spotted parakeratosis.

Course

Self-limiting with spontaneous resolution after 4-8 weeks (possibly with hyperpigmentation but no scarring), can last longer.

Complications

Relapse rate up to 26% in 4 years. 

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Different relapse rates are reported (1-3% up to 26% in 4 years).

Diagnosis

Clinical.

Criteria:

  • herald patch
  • peripheral collarette scales
  • predominant truncal and proximal limb distribution of the lesions, and
  • orientation of lesions along the lines of cleavage 

Differential Diagnosis

Prevention & Therapy

No evidence of any preventive measurements or effective treatment. Mild skin care and avoidance of irritating factors. If pruritic, topical antipruritic agents: weak corticosteroids or emollients. In selected cases narrow band UVB.

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No evidence of any preventive measurements or effective treatment.

Mild skin care and avoidance of irritating factors. If pruritic, topical anti-pruritic agents: mild corticosteroids or emollients. In selected cases UVB 311nm.

Statins and antihistaminics, which induce a sebostatic effect, may enhance the disease severity.

Special

Relapses can especially occur in pregnancy. If in the first 15 weeks, close follow-up is required due to reported miscarriages.

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