eMedicine Specialties > Pediatrics: General Medicine > Dermatology

Zoster

Author: Camila K Janniger, MD, Clinical Professor of Dermatology, Clinical Associate Professor of Pediatrics, Chief of Pediatric Dermatology, New Jersey Medical School
Coauthor(s): Andrea N Driano, MD, Consulting Staff, Department of Emergency Medicine, Children's Hospital and Medical Center, Seattle WA
Contributor Information and Disclosures

Updated: Apr 8, 2009

Introduction

Background

Herpes zoster (shingles) is an acute cutaneous viral infection caused by the reactivation of varicella-zoster virus (VZV), a herpes virus that initially produces chickenpox. After resolution of the primary VZV (chickenpox) infection, the virus lays dormant in the dorsal root ganglion until it undergoes local dermatomal reactivation in the form of herpes zoster (shingles).

The factors that induce the VZV (chickenpox) to reactivate are uncertain. Herpes zoster (shingles) is infrequent in healthy children. However, diminished cellular immunity seems to increase risk of reactivation because incidence increases with age and in immunocompromised states.


Herpes zoster, unilateral, trunk.

Herpes zoster, unilateral, trunk.

Herpes zoster, unilateral, trunk.

Herpes zoster, unilateral, trunk.


Pathophysiology

Herpes zoster (shingles) is a cutaneous viral infection; patients present with a vesicular rash that generally involves the skin of a single unilateral dermatome. Approximately 4-5 days before the eruption appears, the patient may experience preeruptive pain, itching, or burning along the affected dermatome.

Historically, herpes zoster (shingles) was thought to be an indicator for an underlying malignancy. More recent studies have shown no increased incidence of malignancy in children with herpes zoster (shingles). Approximately 3% of pediatric zoster cases occur in children with malignancies. Because of this evidence, a malignancy workup is not indicated in an otherwise healthy child who has herpes zoster (shingles).

Frequency

United States

Herpes zoster (shingles) is uncommon in childhood. More than 66% of patients are older than 50 years. Of all patients with zoster, fewer than 10% are younger than 20 years, and 5% are younger than 15 years. Although zoster is primarily a disease of adults, it has been noted as early as the first week of life. This occurs in infants born to mothers who had primary VZV (chickenpox) infection during pregnancy.

Incidence of the disease increases with age throughout childhood and adult life. Lifetime incidence is 10-20%. Approximately 25% of patients with human immunodeficiency virus (HIV) and 7-9% of patients receiving renal transplantation and cardiac transplantation experience a bout of zoster. Recurrent herpes zoster (shingles) occurs almost exclusively among people who are immunosuppressed.

In the United States, zoster occurs in 300,000-500,000 individuals annually. Nearly 100% of American adults are seropositive for VZV (chickenpox) antibodies. Since routine use of the live attenuated varicella vaccine began in 1994, preliminary observations have revealed that zoster frequency is significantly higher among children who had natural exposure to VZV (chickenpox), compared with those who were vaccinated.

Race

Blacks are 25% less likely than whites to develop herpes zoster (shingles).

Sex

Men and women are equally affected.

Age

Incidence increases with age. From birth to age 9 years, annual incidence is 0.74 cases per 1000 population; in persons aged 10-19 years, annual incidence is 1.38 cases per 1000 population; and in persons aged 20-29 years, annual incidence is 2.58 cases per 1000 population.

Clinical

History

  • Children commonly experience systemic symptoms before cutaneous manifestations erupt. Acute phase symptoms include the following:
    • Pain: This may occasionally be so severe that it may mimic appendicitis, renal calculi, or biliary colic.
    • Pruritus
    • Low-grade fever
    • Malaise
    • Headache
    • Regional lymphadenopathy
  • Patients with multiple myeloma and colon cancer treated with arsenic trioxide may have a propensity to develop herpes zoster (shingles). Arsenic compounds have been suggested as a possible predisposing factor for herpes viral reactivation in these patients.1
  • Herpes zoster (shingles) in childhood is unusual.2 This reactivation of varicella zoster virus (VZV) is seen with increased frequency in otherwise healthy children who acquire VZV (chickenpox) either in utero or within the first year of life.
  • VZV (chickenpox) infection may produce a facial palsy in children.3 It may also result in zoster sine herpete and does so more frequently in children than adults. In one survey of children, Ramsay Hunt syndrome tended to be found in school-aged children, and zoster sine herpete was often found in preschool children.
  • Ambilateral reactivation of herpes zoster V2 following cataract operation of both eyes has been described.4

Physical

  • A unilateral dermatomal eruption begins as grouped vesicles on an erythematous base. These round-to-oval red lesions with surmounting clear fluid-filled blisters usually measure several centimeters in diameter and are oriented along the track of dermatomal innervation. Over the ensuing days, the fluid becomes cloudy and pustular, and, finally, with rupture of the blisters, grouped crusted erosions are left. Thoracic dermatomes are the most common site, and involvement of multiple contiguous dermatomes is common. Lesions erupt over 7 days and develop a crust by 14-21 days.
  • Approximately 17-35% of patients with herpes zoster also have a few scattered vesicles in sites remote from the primary dermatome. This is likely secondary to viremia and should not be confused with generalized herpes zoster (shingles). The generalized form occurs in 2-10% of patients with herpes zoster (shingles).
  • Physical examination should include a slit lamp examination for corneal findings if lesions are found in the distribution of the V1 branch of the trigeminal nerve.
  • Zoster sine herpete appears as a tender erythematous unilateral patch or plaque without vesicle or bullae formation. It tends to be preceded by dysthesias, as is typical herpes zoster (shingles).
  • Herpes zoster ophthalmicus can be initially evident in the eyelids.5 Careful follow-up with attention to the eyelids and eyelid eversion is recommended in patients with herpes zoster to detect early ocular involvement.

Causes

Although VZV (chickenpox) reactivates for unknown reasons, childhood herpes zoster (shingles) has several recognized risk factors. These include the following:

  • Acute lymphocytic leukemia and other malignancies
  • Immunocompromised state as a result of treatments or human immunodeficiency virus (HIV)
  • Immune reconstitution inflammatory syndrome: This is a paradoxical deterioration in clinical status in a patient on antiretroviral treatment despite satisfactory control of viral replication and improvement of CD4 count, may be evident with herpes zoster; early recognition and prompt treatment, along with continuation of highly active antiretroviral treatment, are especially important in this case.6
  • In utero varicella exposure
  • Primary VZV infection (chickenpox) that occurred in the first year of life
  • Antitumor necrosis factor alpha agents (may pose an increased risk)7

More on Zoster

Overview: Zoster
Differential Diagnoses & Workup: Zoster
Treatment & Medication: Zoster
Follow-up: Zoster
Multimedia: Zoster
References

References

  1. Nouri K, Ricotti CA Jr, Bouzari N, Chen H, Ahn E, Bach A. The incidence of recurrent herpes simplex and herpes zoster infection during treatment with arsenic trioxide. J Drugs Dermatol. Feb 2006;5(2):182-5. [Medline].

  2. Papadopoulos AJ, Birnkrant AP, Schwartz RA, Janniger CK. Childhood herpes zoster. Cutis. Jul 2001;68(1):21-3. [Medline].

  3. Ogita S, Terada K, Niizuma T, Kosaka Y, Kataoka N. Characteristics of facial nerve palsy during childhood in Japan: frequency of varicella-zoster virus association. Pediatr Int. Jun 2006;48(3):245-9. [Medline].

  4. Korber A, Franckson T, Grabbe S, Dissemond J. Ambilateral reactivation of herpes zoster V2 following cataract operation of both eyes. J Eur Acad Dermatol Venereol. May 2007;21(5):712-3. [Medline].

  5. Najjar DM, Youssef OH, Flanagan JC. Palpebral subconjunctival hemorrhages in herpes zoster ophthalmicus. Ophthal Plast Reconstr Surg. Mar-Apr 2008;24(2):162-4. [Medline].

  6. Sharma A, Makrandi S, Modi M, Sharma A, Marfatia Y. Immune reconstitution inflammatory syndrome. Indian J Dermatol Venereol Leprol. Nov-Dec 2008;74(6):619-21. [Medline].

  7. Strangfeld A, Listing J, Herzer P, et al. Risk of herpes zoster in patients with rheumatoid arthritis treated with anti-TNF-alpha agents. JAMA. Feb 18 2009;301(7):737-44. [Medline].

  8. Koh MJ, Seah PP, Teo RY. Zosteriform herpes simplex. Singapore Med J. Feb 2008;49(2):e59-60. [Medline].

  9. Kalpoe JS, Kroes AC, Verkerk S, et al. Clinical relevance of quantitative varicella-zoster virus (VZV) DNA detection in plasma after stem cell transplantation. Bone Marrow Transplant. Jul 2006;38(1):41-6. [Medline].

  10. Boer A, Herder N, Blodorn-Schlicht N, Falk T. Herpes incognito most commonly is herpes zoster and its histopathologic pattern is distinctive!. Am J Dermatopathol. Apr 2006;28(2):181-6. [Medline].

  11. Khaliq W, Alam S, Puri N. Topical lidocaine for the treatment of postherpetic neuralgia. Cochrane Database Syst Rev. 2007;(2):CD004846. [Medline].

  12. Caple J. Varicella-zoster virus vaccine: a review of its use in the prevention of herpes zoster in older adults. Drugs Today (Barc). Apr 2006;42(4):249-54. [Medline].

  13. van Hoek AJ, Gay N, Melegaro A, Opstelten W, Edmunds WJ. Estimating the cost-effectiveness of vaccination against herpes zoster in England and Wales. Vaccine. Feb 25 2009;27(9):1454-67. [Medline].

  14. Dworkin RH, White R, O'Connor AB, Hawkins K. Health care expenditure burden of persisting herpes zoster pain. Pain Med. Apr 2008;9(3):348-53. [Medline].

  15. Coen PG, Scott F, Leedham-Green M, et al. Predicting and preventing post-herpetic neuralgia: are current risk factors useful in clinical practice?. Eur J Pain. Nov 2006;10(8):695-700. [Medline].

  16. Courter BJ. Pediatric herpes zoster with mild cutaneous dissemination. Pediatr Emerg Care. Feb 1993;9(1):33-5. [Medline].

  17. Kucukardali Y, Solmazgul E, Terekeci H, Oncul O, Turhan V. Herpes zoster ophthalmicus and syndrome of inappropriate antidiuretic hormone secretion. Intern Med. 2008;47(5):463-5. [Medline].

  18. Lopez N, Alcaraz I, Cid-Manas J, et al. Wolf's isotopic response: zosteriform morphea appearing at the site of healed herpes zoster in a HIV patient. J Eur Acad Dermatol Venereol. Mar 18 2008;[Medline].

  19. Piette ML. Herpes zoster at school-age: a case presentation and discussion of the unique aspects within the pediatric population. Hawaii Med J. Jul 1996;55(7):118-21. [Medline].

  20. Quan D, Hammack BN, Kittelson J, Gilden DH. Improvement of postherpetic neuralgia after treatment with intravenous acyclovir followed by oral valacyclovir. Arch Neurol. Jul 2006;63(7):940-2. [Medline].

  21. Smith CG, Glaser DA. Herpes zoster in childhood: case report and review of the literature. Pediatr Dermatol. May-Jun 1996;13(3):226-9. [Medline].

  22. Straus SE. Overview: the biology of varicella-zoster virus infection. Ann Neurol. 1994;35 Suppl:S4-8. [Medline].

  23. Wung PK, Holbrook JT, Hoffman GS, et al. Herpes zoster in immunocompromised patients: incidence, timing, and risk factors. Am J Med. Dec 2005;118(12):1416. [Medline].

  24. Wurzel CL, Kahan J, Heitler M, Rubin LG. Prognosis of herpes zoster in healthy children. Am J Dis Child. May 1986;140(5):477-8. [Medline].

Further Reading

Keywords

zoster, herpes zoster, shingles, varicella-zoster virus, VZV, chickenpox, vesicular rash, human immunodeficiency virus, HIV, cardiac transplant, renal transplant, appendicitis, renal calculi, biliary colic, myeloma, colon cancer, lymphadenopathy, treatment, diagnosis

Contributor Information and Disclosures

Author

Camila K Janniger, MD, Clinical Professor of Dermatology, Clinical Associate Professor of Pediatrics, Chief of Pediatric Dermatology, 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)

Andrea N Driano, MD, Consulting Staff, Department of Emergency Medicine, Children's Hospital and Medical Center, Seattle WA
Disclosure: Nothing to disclose.

Medical Editor

Kevin P Connelly, DO, Clinical Assistant Professor, Department of Pediatrics, Division of General Pediatrics and Emergency Care, Virginia Commonwealth University; Medical Director, Paws for Health Pet Visitation Program of the Richmond SPCA; Pediatric Emergency Physician, Emergency Consultants Inc, Chippenham Medical Center
Kevin P Connelly, DO is a member of the following medical societies: American Academy of Pediatrics, American College of Osteopathic Pediatricians, and American Osteopathic Association
Disclosure: Nothing to disclose.

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine
Disclosure: Pfizer Inc Stock Investment from financial planner; Avanir Pharma Stock Investment from financial planner ; WebMD Salary and stock Employment and investment from financial planner

Managing Editor

Robert A Schwartz, MD, MPH, Professor and Head, Dermatology, Professor of Pathology, Pediatrics, Medicine, and Preventive Medicine and Community Health, UMDNJ-New Jersey Medical School
Robert A Schwartz, MD, MPH is a member of the following medical societies: Alpha Omega Alpha, American Academy of Dermatology, American College of Physicians, and Sigma Xi
Disclosure: Nothing to disclose.

CME Editor

Merrily P M Poth, MD, Professor, Department of Pediatrics and Neuroscience, Uniformed Services University of the Health Sciences
Merrily P M Poth, MD is a member of the following medical societies: American Academy of Pediatrics, Endocrine Society, and Lawson-Wilkins Pediatric Endocrine Society
Disclosure: Nothing to disclose.

Chief Editor

Dirk M Elston, MD, Director, Department of Dermatology, Geisinger Medical Center
Dirk M Elston, MD is a member of the following medical societies: American Academy of Dermatology
Disclosure: Nothing to disclose.

 
 
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