Atopic Dermatitis
Basics
- Chronic, relapsing, inflammatory, intensely pruritic skin disease.
- Early-onset cases often show allergen sensitization.
- Variable clinical phenotypes indicating multifactorial pathophysiology.
- Significant quality of life impact on patient and family.
Epidemiology
- 45% of cases begin within first 6 months; 80-95% onset before age 5.
- 50-66% remit spontaneously before adolescence.
- Late-onset or relapse in adults mainly as hand eczema.
- More common in darker pigmented individuals.
- Familial aggregation: 60% risk if one parent affected, 80% if both; 80% concordance in monozygotic twins.
- Prevalence ~20% in children, 10% in young adults, 2% in later adulthood.
Etiology and Pathophysiology
- Systemic T-helper cell driven disorder.
- Stratum corneum alteration β increased transepidermal water loss β barrier dysfunction.
- Reduced epidermal adhesion due to genetic mutation (filaggrin gene - FLG) or immune dysregulation.
- IL-31 upregulation mediates pruritus via cytokines and neuropeptides, not histamine.
Risk Factors
- Itch-scratch cycle perpetuates inflammation.
- Skin infections, emotional stress, irritating clothes/chemicals.
- Climate extremes (hot/cold).
- Food allergies (association unclear).
- Tobacco smoke exposure.
- High mineral content water exposure possibly exacerbates.
- Family history of atopy, asthma, allergic rhinitis.
Commonly Associated Conditions
- Food allergies.
- Asthma and allergic rhinitis (atopic march).
- Cutaneous and extracutaneous infections (URI, otitis media, UTI, cellulitis, erysipelas, zoster).
- Hyper-IgE syndrome (Job syndrome).
Diagnosis
History
- Chronic relapsing course.
- Major symptoms: itching (54%), dryness/scaling (19.6%), inflamed skin (7.2%), skin pain (8.2%), sleep disturbance (11.4%).
Physical Exam
- Lesion distribution:
- Infants: face, trunk, extensor surfaces; diaper area spared.
- Children: antecubital/popliteal fossae, wrists, ankles.
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Adults: hands, feet, face, neck, upper chest, genitalia, flexor surfaces.
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Lesion morphology:
- Infants: erythema, papules, oozing, crusting vesicles.
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Children/adults: lichenification, scaling from chronic scratching.
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Associated signs: facial erythema, perioral pallor, Dennie-Morgan folds, dry skin/ichthyosis, palmar markings, pityriasis alba, keratosis pilaris.
Differential Diagnosis
- Photosensitivity rashes
- Contact dermatitis (especially facial)
- Scabies
- Seborrheic dermatitis (infants)
- Psoriasis, lichen simplex chronicus (localized adult eczema)
- Rare infantile conditions (histiocytosis X, Wiskott-Aldrich, ataxia-telangiectasia, ichthyosis vulgaris)
Diagnostic Tests
- No definitive diagnostic test.
- Serum IgE elevated in ~80%, not routinely required.
- Eosinophilia correlates with severity.
- SCORAD (Scoring Atopic Dermatitis) evaluates extent and symptoms.
Treatment
General Measures
- Avoid irritants (wool, perfumes).
- Minimize sweating.
- Lukewarm baths; minimum twice weekly; post-bath emollients.
- Use mild acidic (pH 5-6) hypoallergenic cleansers.
- Humidify living spaces; avoid excessive water exposure.
- Avoid alcohol-containing lotions.
- Screen for coexisting contact dermatitis if resistant.
Pediatric Considerations
- Potent fluorinated corticosteroids may cause striae, hypopigmentation, atrophy.
Medication
- First line:
- Frequent application of thick emollients (Eucerin, Vaseline) over moist skin ("soak and seal").
- Topical corticosteroids:
- Infants/children: short courses moderate potency (hydrocortisone valerate 0.2%, 0.5-1%).
- Adults: higher potency corticosteroids sparingly; avoid face and folds.
- Topical immunomodulators (tacrolimus, pimecrolimus) for children >2 years; may combine with steroids.
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Antihistamines (hydroxyzine) limited benefit for itch.
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Second line:
- Crisaborole (PDE-4 inhibitor) twice daily topical ointment, FDA-approved β₯3 months age; expensive.
- Plastic occlusion to improve absorption (not for face).
- Topical doxepin 5% cream for itch.
- Modified Goeckerman regimen (tar + UV light).
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Treat secondary bacterial infection promptly.
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Biologic therapy:
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Dupilumab (IL-22, IL-17, IFN-Ξ³ pathway inhibitor), FDA-approved β₯6 months old, weekly injections, costly.
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American Academy of Dermatology recommends against routine antibiotics without infection, oral/injectable steroids, and allergy testing unless indicated.
Issues for Referral
- Ophthalmology for vernal conjunctivitis or prolonged periocular steroid use (cataract risk).
- Dermatology for systemic immunotherapy (cyclosporine, azathioprine, methotrexate) in severe disease or quality of life impact.
Additional Therapies
- Environmental allergen control: mite-proof bedding, HVAC filters.
- Behavioral relaxation therapy to reduce scratching.
- Bleach baths (1/2 cup 6% bleach per tub water, 5-10 min soak) - evidence limited.
Complementary & Alternative Medicine
- Evening primrose oil (fatty acids) may reduce prostaglandin synthesis.
- Probiotics may reduce severity and medication use.
Ongoing Care
- Monitor for secondary bacterial/fungal infection; treat clinically evident infections especially Staphylococcus aureus.
Diet
- Trial elimination diets to identify triggers.
- Breastfeeding with maternal hypoallergenic diet may reduce infant severity.
Patient Education
- Refer to American Academy of Dermatology and National Eczema Association resources.
Prognosis
- Chronic condition improving with age; 90% pediatric resolution by puberty.
- Localized eczema may persist in adults.
Complications
- Cataracts (especially with steroids).
- Skin infections, including eczema herpeticum (HSV infection causing severe illness).
- Atrophy or striae from topical steroids, especially with occlusion or potent fluorinated steroids.
ICD10 Codes:
- L20.9 Atopic dermatitis, unspecified
- L20.89 Other atopic dermatitis
- L20.83 Infantile (acute) (chronic) eczema
Clinical Pearls:
- Early and proactive treatment reduces inflammation and complications.
- Use lowest potency steroid effective.
- Monitor for secondary infection.
- Frequent emollient use on moist skin is foundational therapy.