Varicella in Adult
VZV is an acute, serious viral infection when it occurs in adults. In adults, a 2- to 3-day prodrome of fever, chills, irritability, headache, and myalgias may occur. However, skin lesions are usually the initial manifestation of the disease: an acute eruption of pruritic, erythematous macules and papules that start on the face, oral mucosa, and scalp and spread to the trunk and extremities. The lesions rapidly evolve into 1- to 3-mm vesicles with clear serous fluid on an erythematous background. The hallmark of chickenpox is the presence of lesions in various stages of development. Older lesions will evolve to form pustules and serous crusts that heal within 10 days of time. Fever is variable, usually less than 38.9°C (102°F), but can be anywhere from normal to 40.6°C (105°F) in severe cases.
The most common complication is secondary infection of lesions with Staphylococcus or beta-hemolytic Streptococcus. The streptococcal infection can progress to necrotizing fasciitis. Varicella pneumonia is more common in adults, can lead to adult respiratory distress syndrome, and has an overall mortality rate between 10% and 30%. According to the US Centers for Disease Control and Prevention (CDC), adults have a 25-fold greater mortality risk compared with children aged 1-4.
Less common complications include purpura fulminans and thrombocytopenia with protein S deficiency, orchitis, hepatitis, uveitis, arthritis, myocarditis, nephritis, macular atrophy, gastrointestinal bleeding, bacterial pneumonia, protein-losing enteropathy, and Reye syndrome. Central nervous system (CNS) complications occur rarely. These include aseptic meningitis, dystonia, myelitis, cerebellar ataxia, Guillain-Barré, and encephalitis. The cerebellar form of encephalitis has a high mortality rate in adults.
One varicella episode usually confers lifelong immunity, although reinfections have been documented.
In vaccinated individuals, "breakthrough varicella" can occur. Illness is usually mild (low fever or no fever, fewer lesions [less than 50], less pruritic, shorter duration, absence of vesicles), although some patients present similar to unvaccinated individuals.
Patients are considered contagious for 2-5 days before the onset of cutaneous lesions and for 6 days after the last crop has appeared.
Prior to the clinical implementation of the varicella vaccine, approximately 100 deaths per year in the United States were attributed to acute varicella. The highest incidence is from March to May.
Immunocompromised Patient Considerations
Pregnant patients may be at increased risk for severe illness from varicella. Maternal varicella in the first 20 weeks of pregnancy is associated with a 2% risk of fetal damage. If maternal varicella occurs near the time of delivery, the neonate is at risk for severe neonatal varicella.
Varicella may be severe in human immunodeficiency virus (HIV)-infected and other immunocompromised individuals (particularly those with lymphoma and those receiving immunosuppressive therapy, including systemic steroid therapy), with a 7%-10% mortality rate. These patients often have a more extensive (disseminated) and atypical eruption (often with purpura and hemorrhagic vesicles) as well as visceral involvement (CNS, lung, liver). HIV-infected patients have a 7-15 times greater risk of developing herpes zoster.
B01.9 – Varicella without complication
38907003 – Varicella
Differential Diagnosis & Pitfalls
- Herpes simplex virus (HSV) – Grouped vesicles on an erythematous base. Request direct fluorescence antibody (DFA) testing (DFA HSV, in contrast to DFA VZV) and viral culture. Look for more localized lesions in HSV at site of primary infection.
- Hand-foot-and-mouth disease (Coxsackie virus) – Look for vesicular eruption of palms and soles.
- Impetigo – Honey-colored crusts with larger plaques and erosions.
- Rickettsialpox – Check serologies; transmitted by the mouse mite.
- Pityriasis lichenoides et varioliformis acuta (PLEVA) – Asymptomatic crops of erythematous papules that spontaneously resolve within weeks and recur at a later time.
- Bullous drug eruption – Vesicular / bullous lesions. Eosinophilia on CBC and histology are often seen (but not an invariable finding). Look for NSAIDs, sulfonamides, and penicillin medication history.
- Contact dermatitis – Does not have prodromal symptoms and will be localized to site of contact (in contrast to disseminated distribution seen in VZV).
- Vasculitis – Check for rheumatoid factors (RF), antinuclear antibodies (ANA), anti-double-stranded DNA, antineutrophil cytoplasmic antibodies (ANCA), cryoglobulins, C3 and C4 levels and clinical course that does not resolve over several weeks.
- Eczema herpeticum – Hemorrhagic crusted papules and vesicles overlying eczematous skin, usually on the face.
- Insect bite reactions – Larger papules and vesicles; lesions do not rapidly progress to pustules and crusts; favor exposed sites.
- Molluscum contagiosum – No viral symptoms; lesions do not rapidly progress to pustules and crusts.
- Echo virus
- Variola (smallpox) – All lesions at the same stage; favors extremities. Note: this disease has been eradicated; therefore, it would only be diagnosed in the event of a bioterrorist act.