Pityriasis rosea is a type of skin rash.[2] Classically, it begins with a single red and slightly scaly area known as a "herald patch".[2] This is then followed, days to weeks later, by an eruption of many smaller scaly spots; pinkish with a red edge in people with light skin and greyish in darker skin.[4] About 20% of cases show atypical deviations from this pattern.[3] It usually lasts less than three months and goes away without treatment.[3] Sometimes malaise or a fever may occur before the start of the rash or itchiness, but often there are few other symptoms.[3]
While the cause is not entirely clear, it is believed to be related to human herpesvirus 6 (HHV6) or human herpesvirus 7 (HHV7).[3] It does not appear to be contagious.[3] Certain medications may result in a similar rash.[3] Diagnosis is based on the symptoms.[2]
Evidence for specific treatment is limited.[3] About 1.3% of people are affected at some point in time.[3] It most often occurs in those between the ages of 10 and 35.[2] The condition was described at least as early as 1798.[1]
In most cases, a single, 2 to 10cm (1" to 4") oval red "herald" patch appears, classically on the trunk or neck, having an appearance similar to ringworm.[9] 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.
After the herald patch appears, usually some days or weeks later, a rash of many small (5–10mm; 1⁄4" to 1⁄2") pink or red, flaky, oval or round spots appear. They are mostly situated on the trunk and upper limbs. They follow the skin's cleavage lines, which on the upper chest and back produce a characteristic "christmas-tree" distribution.[9]
In 6% of cases an "inverse" distribution may occur, with rash mostly on the extremities.[10] In children, presentation can be atypical or inverse, and the course is typically milder.[11][12]
About one in four people with PR have 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.[13]
About a fifth of cases have an atypical form, with significant variations in symptoms including the size, distribution, morphology, and evolution of the lesions.[14][15] In addition to typical papules and scales, forms appearing as very large plaques (pityriasis rosea gigantea), urticaria, large blisters, patches resembling erythema multiforme, oral lesions, and various other appearances have been noted.[8] A vesicular form can mimic chicken pox.[15][8] Variations in distribution include inverted forms, with rashes on the face or extremities without appearing on the trunk, as well as more uncommon versions localized to the armpits, groin, or extremities (pityriasis rosea circinata et marginata of Vidal) or unilateral spread.[8]
Causes
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[16] of herpes viruses 6 and 7, which cause roseola in infants,[17][18][19][20] though some investigations have found no evidence of this.[21]
Diagnosis
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.[22] Classical symptoms are usually straightforward to recognize, but the wide range of atypical forms may cause difficulty for the clinician in diagnosing some cases.[14] Misdiagnosis by nondermatologists is not uncommon.[7] 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.[22][23] The clinical appearance of pityriasis rosea in some cases is similar to that of secondary syphilis, and rapid plasma reagin testing should be performed if there is any clinical concern for syphilis.[24] A biopsy of the lesions will show extravasated erythrocytes within dermal papillae and dyskeratotic cells within the dermis.[22]
A set of validated diagnostic criteria for pityriasis rosea[25][26] is as follows:
A patient is diagnosed as having pityriasis rosea if:
On at least one occasion or clinical encounter, the patient has all the essential clinical features and at least one of the optional clinical features, and
On all occasions or clinical encounters related to the rash, the patient does not have any of the exclusional clinical features.
The essential clinical features are the following:[citation needed]
Discrete circular or oval lesions,
Scaling on most lesions, and
Peripheral collarette scaling with central clearance on at least two lesions.
The optional clinical features are the following:[citation needed]
Truncal and proximal limb distribution, with less than 10% of lesions distal to mid-upper-arm and mid-thigh,
Orientation of most lesions along skin cleavage lines, and
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:[citation needed]
Multiple small vesicles at the centre of two or more lesions,
Two or more lesions on palmar or plantar skin surfaces, and
Clinical or serological evidence of secondary syphilis.
Treatment
The condition usually resolves on its own, and treatment is not required.[27] Oral antihistamines or topical steroids may be used to decrease itching.[22] 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, scratching should be avoided. It is possible that scratching can make itching worse and an itch–scratch cycle may develop with regular scratching (that is, the patient itches more because they scratch, so they scratch more because they itch, and so on). Irritants such as soaps with fragrances, chlorinated water, wool, and synthetic fabrics should be avoided. Lotions that help stop or prevent itching may be helpful.[27][28]
Direct sunlight makes the lesions resolve more quickly.[22] According to this principle, medical treatment with ultraviolet light has been used to hasten resolution,[29] though studies disagree whether it decreases itching[29] or not.[30] UV therapy is most beneficial in the first week of the eruption.[29]
A 2007 meta-analysis concluded that there is insufficient evidence for the effectiveness of most treatments.[31][needs update] Oral erythromycin was found to be effective for treating the rash and relieving the itch based on one early trial; however, a later study could not confirm these results.[6][31][32]
Prognosis
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. In a ten-year epidemiological study of 939 people in the United States, less than two percent had a recurrence.[33]
Epidemiology
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.[22] It is more common in spring.[22]
↑ Onalaja, Amanda A.; Taylor, Susan C. (2021). "1. Defining skin color". In Li, Becky S.; Maibach, Howard I. (eds.). Ethnic Skin and Hair and Other Cultural Considerations. Switzerland: Springer. p.10. ISBN978-3-030-64829-9.
↑ CHUANG, TSU-YI; PERRY, H.O.; ILSTRUP, D.M.; KURLAND, L.T. (May 1983). "Recent upper respiratory tract infection and pityriasis rosea: a case-control study of 249 matched pairs". British Journal of Dermatology. 108 (5): 587–591. doi:10.1111/j.1365-2133.1983.tb01061.x. PMID6849825. S2CID11253684.
1 2 Sharma PK, Yadav TP, Gautam RK, Taneja N, Satyanarayana L (2000). "Erythromycin in pityriasis rosea: A double-blind, placebo-controlled clinical trial". Journal of the American Academy of Dermatology. 42 (2 Pt 1): 241–4. doi:10.1016/S0190-9622(00)90132-4. PMID10642679.
↑ Tay YK, Goh CL (1999). "One-year review of pityriasis rosea at the National Skin Centre, Singapore". Annals of the Academy of Medicine, Singapore. 28 (6): 829–31. PMID10672397.
↑ Trager, Jonathan D. K. (2007-04-01). "What's your diagnosis? Scaly pubic plaques in a 2-year-old girl--or an "inverse" rash". Journal of Pediatric and Adolescent Gynecology. 20 (2): 109–111. doi:10.1016/j.jpag.2006.12.005. ISSN1083-3188. PMID17418397.
↑ Board basics: an enhancement to MKSAP 17. Alguire, Patrick C. (Patrick Craig), 1950-, Paauw, Douglas S. (Douglas Stephen), 1958-, American College of Physicians (2003- ). [Philadelphia, Pa.]: American College of Physicians. 2015. ISBN978-1938245442. OCLC923566113.{{cite book}}: CS1 maint: others (link)
1 2 3 4 5 6 7 8 Habif, Thomas P (2004). Clinical Dermatology: A Clinical Guide to Diagnosis and Therapy (4thed.). Mosby. pp.246–8. ISBN978-0-323-01319-2.
↑ Horn T, Kazakis A (1987). "Pityriasis rosea and the need for a serologic test for syphilis". Cutis. 39 (1): 81–2. PMID3802914.
↑ Board basics: an enhancement to MKSAP 17. Alguire, Patrick C. (Patrick Craig), 1950-, Paauw, Douglas S. (Douglas Stephen), 1958-, American College of Physicians (2003- ). Philadelphia, Pa.: American College of Physicians. 2015. ISBN978-1938245442. OCLC923566113.{{cite book}}: CS1 maint: others (link)
↑ Chuh AA (2003). "Diagnostic criteria for pityriasis rosea: a prospective case control study for assessment of validity". Journal of the European Academy of Dermatology and Venereology. 17 (1): 101–3. doi:10.1046/j.1468-3083.2003.00519_4.x. PMID12602987. S2CID30400210.
1 2 Chuh, A.; Zawar, V.; Sciallis, G.; Kempf, W. (2016-10-01). "A position statement on the management of patients with pityriasis rosea". Journal of the European Academy of Dermatology and Venereology. 30 (10): 1670–1681. doi:10.1111/jdv.13826. ISSN1468-3083. PMID27406919. S2CID23078602.
1 2 3 Arndt KA, Paul BS, Stern RS, Parrish JA (1983). "Treatment of pityriasis rosea with UV radiation". Archives of Dermatology. 119 (5): 381–82. doi:10.1001/archderm.119.5.381. PMID6847217.
↑ Leenutaphong V, Jiamton S (1995). "UVB phototherapy for pityriasis rosea: a bilateral comparison study". Journal of the American Academy of Dermatology. 33 (6): 996–999. doi:10.1016/0190-9622(95)90293-7. PMID7490372.
↑ Rasi A, Tajziehchi L, Savabi-Nasab S (2008). "Oral erythromycin is ineffective in the treatment of pityriasis rosea". Journal of Drugs in Dermatology. 7 (1): 35–38. PMID18246696.
↑ Chuang TY, Ilstrup DM, Perry HO, Kurland LT (1982). "Pityriasis rosea in Rochester, Minnesota, 1969 to 1978". Journal of the American Academy of Dermatology. 7 (1): 80–9. doi:10.1016/s0190-9622(82)80013-3. PMID6980904.
↑ "Pityriasis rosea". American Osteopathic College of Dermatology. Retrieved 26 Jan 2010.
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