Distinguishing Asteatotic Eczema from Shingles
The key to differentiating asteatotic eczema from shingles lies in the distribution pattern and lesion morphology: shingles presents with grouped vesicles in a unilateral dermatomal distribution with prodromal pain, while asteatotic eczema shows bilateral, symmetric dry, cracked skin with a "crazy paving" pattern, typically on the lower legs.
Clinical Presentation Differences
Shingles (Herpes Zoster) Characteristics
- Prodromal pain precedes skin findings by 24-72 hours, followed by a unilateral vesicular eruption strictly confined to a dermatomal distribution 1, 2
- Lesions progress from erythematous macules to papules and then to grouped vesicles on an erythematous base, continuing to erupt for 4-6 days 1, 2
- The rash is always unilateral and does not cross the midline, with total disease duration of approximately 2 weeks in immunocompetent individuals 1, 2
- Pain is a cardinal feature, though atypical presentations without characteristic pain can occur 2
Asteatotic Eczema Characteristics
- Presents as bilateral, symmetric dry skin with fine cracks creating a "crazy paving" or "craquelé" appearance 3
- Characterized by itching rather than pain, with scratching or rubbing behavior reported 3
- Shows polymorphic features including erythema, scale, and crust, but lacks the grouped vesicular pattern of shingles 4
- Commonly affects the lower legs bilaterally, particularly in elderly patients or those with dry skin 3
Diagnostic Algorithm for Patients Over 50 or Immunocompromised
Step 1: Assess Distribution Pattern
- If unilateral and dermatomal: Strongly suggests shingles—proceed to Step 2 1, 2
- If bilateral and symmetric: Favors asteatotic eczema—proceed to Step 3 3
Step 2: Evaluate Lesion Morphology for Suspected Shingles
- Grouped vesicles on erythematous base in dermatomal pattern: Diagnose as shingles clinically and initiate treatment immediately 1, 2, 5
- Atypical presentation (nonspecific lesions, faint rash, or immunocompromised patient): Obtain confirmatory testing with Tzanck preparation, immunofluorescent viral antigen studies, PCR, or viral culture 2
- Initiate oral valacyclovir 1 gram three times daily within 72 hours of rash onset for uncomplicated cases 5
- Escalate to IV acyclovir 10 mg/kg every 8 hours for immunocompromised patients, disseminated disease, or complicated facial involvement 1, 5
Step 3: Confirm Asteatotic Eczema Diagnosis
- Look for history of dry skin, itchiness in skin creases, personal or family history of atopy (asthma, hay fever, or atopic dermatitis) 3
- Examine for general dry skin, visible flexural involvement, and absence of vesicles 3
- If diagnostic uncertainty persists, consider patch testing to rule out allergic contact dermatitis or skin biopsy to exclude other conditions 3, 6
Step 4: Rule Out Complications and Coexisting Conditions
- In patients with atopic dermatitis or eczema, always consider eczema herpeticum (widespread herpes simplex infection), which presents with monomorphic dome-shaped vesicles and pustules in eczematous areas with severe systemic illness 7
- Fever and lymphopenia are associated with eczema herpeticum, requiring immediate antiviral therapy 7
- Deterioration in previously stable eczema may indicate secondary bacterial infection (impetiginization) or development of contact dermatitis 3
Treatment Approach Based on Diagnosis
For Confirmed Shingles
- Oral valacyclovir 1 gram three times daily for 7 days initiated within 72 hours of rash onset for immunocompetent patients 5
- IV acyclovir 10 mg/kg every 8 hours for immunocompromised patients, continuing for minimum 7-10 days until all lesions have completely scabbed 1, 5
- Continue treatment until all lesions have scabbed, not just for an arbitrary 7-day period—this is the key clinical endpoint 1, 5
- Avoid contact with susceptible individuals until all lesions have crusted 5
For Confirmed Asteatotic Eczema
- Liberal use of emollients as the cornerstone of treatment 3
- Topical corticosteroids with potency, site, and extent considerations: age of patient, location to be treated, and disease severity guide selection 3
- Adequate time for patient education regarding application techniques and disease chronicity 3
Critical Pitfalls to Avoid
- Never delay antiviral treatment for shingles while awaiting confirmatory testing in typical presentations—treatment must begin within 72 hours for optimal efficacy 1, 5
- Do not apply topical corticosteroids to suspected shingles, as this can worsen viral replication and increase dissemination risk, particularly in immunocompromised patients 1
- Do not dismiss unilateral dermatomal pain without rash as non-shingles—this may represent early shingles or zoster sine herpete requiring antiviral therapy 1
- In patients with atopic dermatitis presenting with acute worsening, always consider eczema herpeticum, which requires immediate systemic antiviral therapy rather than increased corticosteroids 7
- For immunocompromised patients with any vesicular eruption, obtain viral studies and initiate empiric antiviral therapy pending results, as atypical presentations are common 2