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Shingles and Postherpetic Neuralgia

Symptoms & Signs

  • Zoster
    • Onset of disease is often heralded by pain within the dermatome that may precede eruption of the rash by 2–3 days.
    • Prodrome can also include fever, malaise, and headache.
    • General characteristics of the rash
      • Most commonly involves a single, unilateral nerve root
      • Erythematous maculopapular rash evolves rapidly into vesicular lesions.
      • Lesions may remain few in number.
      • New lesions may continue to form for 3–5 days.
      • Rash is typically very pruritic and painful.
      • Usually lasts 7–10 days, though skin may not heal completely for 2–4 weeks
    • 3 clinical presentations
      • Unilateral vesicular eruption within a dermatome (most frequently between T3 and L3)
      • Zoster ophthalmicus (involvement of ophthalmic branch [V1] of the trigeminal nerve)
        • Pain and rash in the distribution of V1
        • Involvement of the eye is an ophthalmologic emergency.
        • Can lead to blindness if untreated
      • Ramsay Hunt syndrome (involvement of the facial nerve [cranial nerve VII])
        • Pain and vesicles appear in external auditory canal.
        • Ipsilateral facial palsy (upper and lower half of the face, resembling Bell’s palsy)
        • Loss of taste in the ipsilateral anterior two-thirds of the tongue
    • Immunocompromised host
      • Similar clinical presentations, though, can be more prolonged and more severe.
      • In immunocompromised patients who develop disseminated cutaneous zoster, there is the risk of involvement of the lungs (pneumonitis), central nervous system (meningoencephalitis), liver, and other organs.
        • Rarely fatal
  • Postherpetic neuralgia
    • Persistent pain and paresthesias in the dermatomal distribution of previous zoster rash
      • May be sharp, stabbing, burning, or aching
      • Can have either hypoesthesia or hyperesthesia on examination
      • Extreme sensitivity to touch and temperature changes

Differential Diagnosis

Diagnostic Approach

  • Zoster
    • Diagnosis is almost always made by clinical assessment alone without additional laboratory confirmation.
    • Unilateral vesicular lesions in a dermatomal pattern should suggest diagnosis.
    • In prodromal stage, diagnosis can be difficult and may be made only after lesions have appeared or by retrospective serologic assessment.
    • Occurrence of zoster without a rash can occur (zoster sine herpete).
    • Unequivocal confirmation is possible only through 1 of the following:
      • Isolation of VZV in susceptible tissue-culture cell lines
      • Demonstration of either seroconversion or a > 4-fold rise in antibody titer between convalescent- and acute-phase serum specimens
      • Detection of VZV DNA by polymerase chain reaction (PCR)
  • Postherpetic neuralgia
    • Clinical diagnosis: pain syndrome in zoster-affected dermatome following vesicular rash consistent with zoster infection

Laboratory Tests

  • Zoster
    • Serology
      • Unequivocal confirmation of VZV infection if > 4-fold rise in antibody titer between convalescent- and acute-phase serum specimens
      • Most frequently employed serologic tools for assessing host response are:
        • Immunofluorescent detection of antibodies to VZV membrane antigens
        • Fluorescent antibody to membrane antigen (FAMA) test
        • Immune adherence hemagglutination
        • Enzyme-linked immunosorbent assay (ELISA)
      • FAMA test and ELISA appear to be the most sensitive.
    • PCR
      • PCR technology for detection of viral DNA in vesicular fluid
        • Available in a limited number of diagnostic laboratories
    • Tissue cultures
      • Isolation of VZV in susceptible tissue-culture cell lines gives unequivocal confirmation of diagnosis.
  • Postherpetic neuralgia
    • No laboratory tests are indicated.

Imaging

  • Routine imaging is not indicated.

Diagnostic Procedures

  • Zoster
    • Tzanck smear
      • Tzanck smear of scraping from base of lesions to demonstrate multinucleated giant cells is rapid but has low sensitivity (~60%).
    • Cerebrospinal fluid analysis usually is not indicated unless central nervous system involvement is suspected.
      • Asymptomatic meningitis may be present.
        • Pleocytosis
        • Moderately elevated protein levels

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