Pityriasis rosea
- Overview
- Theory
- Diagnosis
- Management
- Follow up
- Resources
Treatment algorithm
Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups: see disclaimer
mild-to-moderate symptoms
reassurance + emollients
Most cases of PR are self-limiting and require no treatment; however, provide reassurance.
Topical emollients may diminish the appearance of scale.[11]Contreras-Ruiz J, Peternel S, Jiménez Gutiérrez C, et al. Interventions for pityriasis rosea. Cochrane Database Syst Rev. 2019 Oct 30;2019(10):CD005068. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819167 http://www.ncbi.nlm.nih.gov/pubmed/31684696?tool=bestpractice.com
antihistamines
Treatment recommended for ALL patients in selected patient group
Oral antihistamines are used to reduce symptoms of pruritus.
Non-sedating antihistamines (e.g., loratadine, fexofenadine, cetirizine) can be given in the morning, while sedating antihistamines (e.g., hydroxyzine) are usually given in the evening.
Primary options
loratadine: 10 mg orally once daily
OR
fexofenadine: 180 mg orally once daily
OR
cetirizine: 10 mg orally once daily
OR
hydroxyzine: 10-25 mg orally once daily at night
low-to-mid-potency topical corticosteroids
Additional treatment recommended for SOME patients in selected patient group
In patient with symptoms causing constant itching that interferes with daily activities, low-to-mid-potency topical corticosteroids may be used, depending on the severity of the rash and symptoms.[11]Contreras-Ruiz J, Peternel S, Jiménez Gutiérrez C, et al. Interventions for pityriasis rosea. Cochrane Database Syst Rev. 2019 Oct 30;2019(10):CD005068. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819167 http://www.ncbi.nlm.nih.gov/pubmed/31684696?tool=bestpractice.com [22]Villalon-Gomez JM. Pityriasis rosea: diagnosis and treatment. Am Fam Physician. 2018 Jan 1;97(1):38-44. https://www.aafp.org/afp/2018/0101/p38.html http://www.ncbi.nlm.nih.gov/pubmed/29365241?tool=bestpractice.com
Primary options
hydrocortisone topical: (2.5%) apply sparingly to the affected area(s) twice daily for 2 weeks
severe or refractory disease
doxepin and/or higher-potency topical corticosteroid
For patients with more severe symptoms, or those unresponsive to lower-potency therapies, more potent antipruritic agents may be beneficial. These include: doxepin, a tricyclic antidepressant with limited evidence to support its use for short-term relief of pruritus; and/or high-potency topical corticosteroids (e.g., triamcinolone).
Primary options
doxepin: 10 mg orally once daily at night; (5% cream) apply to the affected area(s) up to four times daily
and/or
triamcinolone topical: (0.1%) apply sparingly to the affected area(s) twice daily for 2 weeks
narrow-band ultraviolet-B (UVB)
Additional treatment recommended for SOME patients in selected patient group
Narrow-band UVB may be used in severe or refractory disease.[22]Villalon-Gomez JM. Pityriasis rosea: diagnosis and treatment. Am Fam Physician. 2018 Jan 1;97(1):38-44. https://www.aafp.org/afp/2018/0101/p38.html http://www.ncbi.nlm.nih.gov/pubmed/29365241?tool=bestpractice.com
This requires a significant commitment by the patient to attend all sessions. However, there is no good evidence that UVB results in shortening of duration or improvement of symptoms.[11]Contreras-Ruiz J, Peternel S, Jiménez Gutiérrez C, et al. Interventions for pityriasis rosea. Cochrane Database Syst Rev. 2019 Oct 30;2019(10):CD005068. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819167 http://www.ncbi.nlm.nih.gov/pubmed/31684696?tool=bestpractice.com
The mechanism of action of light therapy is cross-linking DNA to prevent DNA synthesis, and inhibiting activity and action of inflammatory cells in the skin.
Most common adverse effects are phototoxicity and small theoretical increased risk of skin cancer if therapy is prolonged.
refractory to all other treatments
systemic corticosteroids
Reserve prednisolone for patients in severe discomfort, and those who are refractory to topical corticosteroids and antihistamines, although such use remains controversial.[11]Contreras-Ruiz J, Peternel S, Jiménez Gutiérrez C, et al. Interventions for pityriasis rosea. Cochrane Database Syst Rev. 2019 Oct 30;2019(10):CD005068. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819167 http://www.ncbi.nlm.nih.gov/pubmed/31684696?tool=bestpractice.com [22]Villalon-Gomez JM. Pityriasis rosea: diagnosis and treatment. Am Fam Physician. 2018 Jan 1;97(1):38-44. https://www.aafp.org/afp/2018/0101/p38.html http://www.ncbi.nlm.nih.gov/pubmed/29365241?tool=bestpractice.com [27]Drago F, Rebora A. Treatments for pityriasis rosea. Skin Therapy Lett. 2009 Mar;14(3):6-7. http://www.skintherapyletter.com/2009/14.3/2.html http://www.ncbi.nlm.nih.gov/pubmed/19585058?tool=bestpractice.com [28]Tay YK, Goh CL. One-year review of pityriasis rosea at the National Skin Centre, Singapore. Ann Acad Med Singapore. 1999 Nov;28(6):829-31. http://www.ncbi.nlm.nih.gov/pubmed/10672397?tool=bestpractice.com
It should be noted that prednisolone may help symptoms, but will not shorten the disease course or improve the clinical appearance of the lesions.
Despite this, it should be noted that some physicians do not advocate the use of prednisolone in PR.
Primary options
prednisolone: 1 mg/kg/day orally for 4 days, followed by gradual taper over 2 weeks, maximum 60 mg/day
Choose a patient group to see our recommendations
Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups. See disclaimer
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