Pityriasis Clinical Presentation

  • Author: Camila K Janniger, MD; Chief Editor: Burke A Cunha, MD   more...
 
Updated: May 16, 2011
 

History

Patients with pityriasis may report a history of nonspecific symptoms (eg, malaise, nausea, fever) that precede the development of the rash.

Obtain a detailed dermatologic history in all patients. Ask patients about prior dermatologic diseases and their manifestations. Elicit symptoms of the presenting rash (eg, pruritus, pain).

When pertinent, obtain a history of sexually transmitted diseases.

Record travel history, occupational exposure, and drug exposure in the medical record.

Ask patients about ill contacts.

The natural history of pityriasis rosea in black children may differ from that described in American, European, and African literature. A study by Amer et al (2007) found that black children with pityriasis rosea had more frequent facial (30%) and scalp lesions (8%) involvement than anticipated in white populations. One third had the papular form of pityriasis rosea.[1]

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Physical

The initial skin lesion of pityriasis is a pink (rosea) oval patch approximately 3-6 cm in diameter that can develop anywhere on the body, including on plantar skin, although it is most commonly located on the back.[2] This is referred to as the herald patch. The herald patch has a scale (pityriasis) that resembles a collarette toward the periphery. The patch is something of a dermatologic enigma because it does not occur in any other known skin disease. The earliest stages of the patch may manifest as pink papules that can be mistaken for other lesions (eg, insect bites).

A few days later, the initial patch is followed by a rash of similar but smaller lesions. Secondary eruptions appear in crops at intervals of a few days and reach a maximum in about 10 days. The rash typically follows the cleavage lines of the skin, resulting in a Christmas tree–type pattern. The secondary rash is generally distributed on the back, chest, abdomen, arms, and thighs. The rash can last up to 6-8 weeks before fading.

Lesions are typically symmetric and are not preceded by systemic symptoms.

Pruritus appears to be the predominant symptom but can be absent in as many as 25% of cases.

Individuals with dark skin can have a postinflammatory hyperpigmentation that may take a few months to heal. Both hypopigmentation and hyperpigmentation can follow the rash.

The following atypical features occasionally occur:

  • Herald patch is absent in 10-50% of cases.
  • Skin eruptions may be florid.
  • Lesions may be few, large, and in a particular body region (eg, axilla). In adults, this is known as pityriasis circinata et marginata of Vidal.
  • Rash may be located in areas not usually affected by pityriasis; this is known as inverse pityriasis rosea.
  • Pityriasis may occur in sun-spared areas such as the breast and the axilla.
  • Lesions are sometimes papular, vesicular, or purpuric.
  • Pityriasis rosea may occur along the lines of Blaschko.[3]

Pityriasis rosea of Vidal is a rare variant in which the eruption appears in the axillae and/or groin and the trunk and extremities usually spared.[4] This variant is also known as "limb-girdle pityriasis rosea." Individual patches are 3-6 cm in diameter, with the characteristic central clearing and collarette of scale with surrounding erythema.

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Causes

  • An infectious etiology for pityriasis rosea has been sought for many years.
  • A viral agent was once postulated as a precipitant for pityriasis rosea. Over the past few years, there has been considerable interest in human herpesvirus 7 as a possible etiologic agent. Investigative studies have failed to link this virus, as well as others, to the well-known rash of pityriasis rosea.[5]
  • Some investigators believe that a fungal infection is more likely.
  • Thus far, the search for an infectious agent has been unsuccessful.
  • The incidence of pityriasis rosea among dermatologists is 3-4 times that of other physicians.
  • Recurrences of pityriasis rosea are generally regarded as rare and are thought by some to indicate a lasting immunity when they do occur.
  • Certain medications have been implicated as possible causes of pityriasis rosea.[6] Adalimumab was recently linked with pityriasis rosea.[7]
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Contributor Information and Disclosures
Author

Camila K Janniger, MD  Clinical Professor of Dermatology, Clinical Associate Professor of Pediatrics, Chief of Pediatric Dermatology, University of Medicine and Dentistry of New Jersey-New Jersey Medical School

Camila K Janniger, MD is a member of the following medical societies: American Academy of Dermatology

Disclosure: Nothing to disclose.

Coauthor(s)

Rajendra Kapila, MD, MBBS  Professor of Medicine, Department of Medicine, UMDNJ, New Jersey Medical School

Rajendra Kapila, MD, MBBS is a member of the following medical societies: American College of Physicians, American Medical Association, Infectious Diseases Society of America, and Infectious Diseases Society of New Jersey

Disclosure: Nothing to disclose.

Robert L Rogers, MD  Staff Physician, Departments of Internal Medicine and Surgery, Division of Emergency Medicine, University of Maryland

Robert L Rogers, MD is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, and American College of Physicians-American Society of Internal Medicine

Disclosure: Nothing to disclose.

Amal Mattu, MD, FACEP, FAAEM  Program Director, Emergency Medicine Residency, Co-Director, Emergency Medicine/Internal Medicine Combined Residency Program, Department of Surgery, Division of Emergency Medicine, University of Maryland School of Medicine

Amal Mattu, MD, FACEP, FAAEM is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, and Society for Academic Emergency Medicine

Disclosure: Nothing to disclose.

Specialty Editor Board

Daniel R Lucey, MD, MPH  Chief, Fellowship Program Director, Department of Internal Medicine, Division of Infectious Diseases, Washington Hospital Center; Professor, Department of Internal Medicine, Uniformed Services University of the Health Sciences

Daniel R Lucey, MD, MPH is a member of the following medical societies: Alpha Omega Alpha and American College of Physicians

Disclosure: Nothing to disclose.

Francisco Talavera, PharmD, PhD  Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: eMedicine Salary Employment

Thomas M Kerkering, MD  Chief of Infectious Diseases, Virginia Tech Carilion School of Medicine

Thomas M Kerkering, MD is a member of the following medical societies: Alpha Omega Alpha, American College of Physicians, American Public Health Association, American Society for Microbiology, American Society of Tropical Medicine and Hygiene, Infectious Diseases Society of America, Medical Society of Virginia, and Wilderness Medical Society

Disclosure: Nothing to disclose.

Eleftherios Mylonakis, MD  Clinical and Research Fellow, Department of Internal Medicine, Division of Infectious Diseases, Massachusetts General Hospital

Eleftherios Mylonakis, MD is a member of the following medical societies: American Association for the Advancement of Science, American College of Physicians, American Society for Microbiology, and Infectious Diseases Society of America

Disclosure: Nothing to disclose.

Chief Editor

Burke A Cunha, MD  Professor of Medicine, State University of New York School of Medicine at Stony Brook; Chief, Infectious Disease Division, Winthrop-University Hospital

Burke A Cunha, MD is a member of the following medical societies: American College of Chest Physicians, American College of Physicians, and Infectious Diseases Society of America

Disclosure: Nothing to disclose.

References
  1. Amer A, Fischer H, Li X. The natural history of pityriasis rosea in black American children: how correct is the "classic" description?. Arch Pediatr Adolesc Med. May 2007;161(5):503-6. [Medline].

  2. Robati RM, Toossi P. Plantar herald patch in pityriasis rosea. Clin Exp Dermatol. Mar 2009;34(2):269-70. [Medline].

  3. Ang CC, Tay YK. Blaschkoid pityriasis rosea. J Am Acad Dermatol. Nov 2009;61(5):906-8. [Medline].

  4. Zawar V, Godse K. Annular groin eruptions: pityriasis rosea of vidal. Int J Dermatol. Feb 2011;50(2):195-7. [Medline].

  5. Kempf W, Adams V, Kleinhans M, et al. Pityriasis rosea is not associated with human herpesvirus 7. Arch Dermatol. Sep 1999;135(9):1070-2. [Medline].

  6. González LM, Allen R, Janniger CK, et al. Pityriasis rosea: an important papulosquamous disorder. Int J Dermatol. Sep 2005;44(9):757-64. [Medline].

  7. Rajpara SN, Ormerod AD, Gallaway L. Adalimumab-induced pityriasis rosea. J Eur Acad Dermatol Venereol. Oct 2007;21(9):1294-6. [Medline].

  8. Chuh AA, Dofitas BL, Comisel GG, et al. Interventions for pityriasis rosea. Cochrane Database Syst Rev. Apr 18 2007;CD005068. [Medline].

  9. Rasi A, Tajziehchi L, Savabi-Nasab S. Oral erythromycin is ineffective in the treatment of pityriasis rosea. J Drugs Dermatol. Jan 2008;7(1):35-8. [Medline].

  10. Krishnamurthy K, Walker A, Gropper CA, Hoffman C. To treat or not to treat? Management of guttate psoriasis and pityriasis rosea in patients with evidence of group A Streptococcal infection. J Drugs Dermatol. Mar 2010;9(3):241-50. [Medline].

  11. Chuang TY, Ilstrup DM, Perry HO, et al. Pityriasis rosea in Rochester, Minnesota, 1969 to 1978. J Am Acad Dermatol. Jul 1982;7(1):80-9. [Medline].

  12. Cohen EL. Pityriasis rosea. Br J Dermatol. Oct 1967;79(10):533-7. [Medline].

  13. Harman M, Aytekin S, Akdeniz S, et al. An epidemiological study of pityriasis rosea in the Eastern Anatolia. Eur J Epidemiol. Jul 1998;14(5):495-7. [Medline].

  14. Hartley AH. Pityriasis rosea. Pediatr Rev. Aug 1999;20(8):266-9, quiz 270. [Medline].

  15. Parsons JM. Management of toxic epidermal necrolysis. Cutis. Oct 1985;36(4):305-7, 310-1. [Medline].

  16. Tay YK, Goh CL. One-year review of pityriasis rosea at the National Skin Centre, Singapore. Ann Acad Med Singapore. Nov 1999;28(6):829-31. [Medline].

  17. Wyndham M. Pityriasis. Practitioner. Jun 1997;241(1575):358. [Medline].

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