Eczema
Eczema, a chronic inflammatory skin disease, impacts approximately 20% of children and 3% of adults, manifesting as
- pruritus
- eczematous lesions (dry, scaling and crusted areas of skin)
- when chronic may be associated with lichenification (thickening) and pigmentary changes
- relapsing course
- varying frequency and periods of remissions
Also referred to as atopic eczema or atopic dermatitis
Background:
- Onset Characteristics:
- Typically begins between 3-6 months
- 60% of cases emerging before age 1
- 90% by age 5.
- Associations: Elevated serum IgE levels and a personal or immediate family history of atopy (type I allergies, allergic rhinitis, and asthma).
Diagnosis:
- Diagnostic Approach: Diagnosis relies on patient history and clinical examination.
- Criteria: Key criteria involve pruritus, eczema, chronic or relapsing history, typical morphology, and age-specific patterns.
4. Diagnostic Features (American Academy of Dermatology):
- Essential Features (Must be Present):
- Pruritus
- Eczema (acute, subacute, chronic)
- Chronic or relapsing history
- Typical morphology and age-specific patterns
- Important Features (Adding Support):
- Early age of onset
- Atopy
- Raised IgE levels
- Associated Features (Suggestive but Nonspecific):
- Various dermatological responses
- Ocular/periorbital changes
- Regional findings
5. Diagnostic Criteria (Hanifin and Rajka, UK Working Party):
- Major Criteria (Must Have 3):
- Pruritus
- Dermatitis affecting flexural surfaces in adults or face and extensor surfaces in infants
- Chronic or relapsing dermatitis
- Personal or family history of cutaneous or respiratory allergy
- Minor Criteria (Must Have 3):
- Facial features
- Triggers (emotional, environmental, food, skin irritants)
- Various complications (skin infections, impaired immunity, etc.)
Differential Diagnosis:
- - Atopic dermatitis
- - Irritant contact dermatitis (detergents, solvents, friction)
- - Allergic contact dermatitis (nickel, perfume, rubber)
- - Dermatitis herpetiformis (coeliac disease)
- - Cow’s milk protein allergy
- - Seborrhoeic dermatitis (scalp)
- - Scabies
- - Tinea
- - Psoriasis
- - Localised herpetic infections
- - Immunodeficiency (Cutaneous T cell lymphoma)
- - Dry skin
- - Molluscum dermatitis
- - Miliaria
- - Zinc deficiency
Differential diagnosis of eczema (not exhaustive) | |
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Other inflammatory dermatoses | Seborrhoeic dermatitis, psoriasis, contact allergy or irritation, pompholyx, napkin dermatitis, nummular eczema, lichen simplex, pityriasis lichenoides acuta and chronica, pityriasis alba |
Ichthyoses | Ichthyosis vulgaris, autosomal recessive congenital ichthyosis, X-linked ichthyosis, Netherton syndrome |
Infections and infestations | Scabies, tinea corporis, pityriasis versicolor, pityriasis rosea, HIV |
Immunodeficiencies | Severe combined immunodeficiency, Omenn syndrome, hyper-IgE syndrome, Wiskott-Aldrich syndrome, IPEX syndrome |
Immunological disorders | Dermatitis herpetiformis, juvenile dermatomyositis, graft-vs-host disease |
Malignancies | Cutaneous T-cell lymphoma (mycosis fungoides) |
Metabolic disorders | Zinc deficiency, pyridoxine deficiency, biotin deficiency, niacin deficiency, phenylketonuria, cystic fibrosis, neutral lipid storage disease |
Other | Urticaria pigmentosa, Epidermolysis bullosa pruriginosa |
Assessment:
- Identification of Triggers:
- Irritants (soaps, detergents, chlorine in swimming pools)
- Skin infections (Staphylococcus aureus, Streptococcus pyogenes, herpes simplex)
- Contact allergens
- Food and inhalant triggers
- Stress
- Assessment of ciurrent and previous Treatments:
- History should cover:
- Bathing/showering frequency
- Use of soap, soap-free cleansers, shampoos
- Use of bath additives
- Emollient/moisturiser—frequency of application, quantity used per week
- Topical steroids—types, sites of application, quantity used per week
- Any adverse reaction to topical agents eg stinging
- Antihistamine, antibiotic use
- Underuse of topical treatments is a common cause of treatment failure in eczema.
- History should cover:
Impact of Eczema:
- Areas of Focus:
- Psychosocial impact
- Skin infections
- Absenteeism from school/activities
- Sleep quality
- Formal Measures: CDLQI, POEMS.
Physical Examination:
- Components:
- Diagnostic features of eczema or other potential diagnoses
- Extent and severity of eczema
- Evidence of secondary infection
- Growth and development monitoring in children
- Formal Measures: SCORAD, EASI.
Investigations: – Instances for Consideration: Some cases may require investigations to confirm the diagnosis and rule out other potential conditions.
Holistic Assessment (NICE Guidelines 2007):
- Skin and physical severity
- Impact on quality of life and psychosocial well-being
- Cultural practices and beliefs of the child and family
Factors Considered: –
Skin and physical severity | Impact on quality of life and psychosocial wellbeing | ||
---|---|---|---|
Clear | Normal skin, no evidence of active eczema | Clear | No impact on quality of life |
Mild | Areas of dry skin, infrequent itching (with or without small areas of redness) | Mild | Little impact on everyday activities, sleep and psychosocial wellbeing |
Moderate | Areas of dry skin, frequent itching, redness (with or without excoriation and localized skin thickening) | Moderate | Moderate impact on everyday activities and psychosocial wellbeing, frequently disturbed sleep |
Severe | Widespread areas of dry skin, incessant itching, redness (with or without excoriation, extensive skin thickening, bleeding, oozing, cracking and alteration of pigmentation) | Severe | Severe limitation of everyday activities and psychosocial impact, nightly loss of sleep |
Outpatient Management:
- Prescribed Elements:
- Advice on trigger/irritant avoidance.
- Guidance on bathing and soap substitutes.
- Emollients (moisturizers).
- Topical corticosteroids/calcineurin inhibitors.
- Antibiotics and antihistamines if necessary.
- Instructions on recognizing infections.
- A clear plan for regular health professional reviews.
Bathing Recommendations:
- Frequency: Once or twice daily.
- Water Conditions: Warm water, baths lasting no more than 10 minutes.
- Products: Emollients or emollient washes instead of soap and shampoo.
- Additional Consideration: Antiseptic baths (bleach baths) or triclosan bath oils may be beneficial.
Emollients/Moisturizers:
- Usage: Provided for daily moisturizing, washing, and bathing.
- Quantity: Children should receive 250–500g of emollient weekly. adult patients may use up to 500 g/week or more
- Application Technique: Emollients are best applied when skin is moist (after bathing) but can and should be applied at other times as well. Ideally, they should be applied every 4 hours or at least 3 to 4 times per day.
- Container Considerations: Prefer pump containers or tubes to prevent contamination.
Topical Corticosteroids:
- Benefits and Harms Discussion: Prioritize a discussion with family/caregivers, emphasizing benefits over potential harms.
- Potency Selection: Use the fingertip unit ( FTP) as a guide to the amount of topical steroid to use different areas of the body. Tailored to eczema severity, with mild, moderate, and potent categories.
- Mild potency
- For mild eczema
- For infants <12 months
- For the face and neck
- Moderate potency
- For moderate eczema
- For short term 5–7 day use in the axillae and groin and for severe facial flares
- Potent
- For severe eczema
- Not recommended for use on the face and neck
- Do not use super potent topical corticosteroids in children (or potent in children under the age of 12 months) without specialist dermatological advice
- Mild potency
- Topical corticosteroids should only be applied to areas of active eczema, and stopped when the eczema has gone.
- Emollients should be continued.
- Topical corticosteroids should be applied in a thin layer to the affected area once or twice daily.
- They can be applied before or after emollients.
- Diluting topical corticosteroids in emollient or other products has not been shown to reduce potency.
- Long term continuous use of topical steroids can rarely result in side effects
- skin thinning
- adrenal suppression with widespread application.
- It is recommended that children using topical steroids are reviewed regularly and treatment stepped down in frequency as possible.
- Children requiring continuous use of topical steroid should be reviewed by a dermatologist.
- Long term maintenance use of topical steroids 2 days per week (‘weekend treatment’) seems safe and effective
Topical Calcineurin Inhibitors:
- Consideration: Second-line therapy for eczema unresponsive to topical corticosteroids.
- Discussion with Caregivers: Risks and benefits should be thoroughly discussed.
- Specialist Involvement: Recommended, and not to be used without dermatological advice.
Antihistamines:
- Routine Use Not Recommended: Not for routine use. Oral non-sedating antihistamines may provide relief for some patients, particularly those with concomitant urticaria or allergic rhinitis.
- Consideration for Trial: Short-term use (<1 month) for moderate-severe eczema or associated urticaria.
- Review: Evaluate benefits every 3 months.
Antibiotics:
- Topical Use: Limited to localized areas (<5 cm) for up to 7 days.
- Systemic Use: A 7-day course of oral flucloxacillin is most appropriate for treating Staphylococcus aureus.
- Other: Soaking for 10 minutes twice weekly in dilute bleach bath (sodium hypochlorite) may reduce the severity of eczema and skin infections.
Reassessment After 7–14 Days:
- Considerations for No Improvement:
- Incomplete adherence to treatments.
- Ongoing exposure to irritants.
- Inadequate application of corticosteroid.
- Secondary skin infection.
- Contact allergy or incorrect diagnosis.
Treatment of refractory eczema | |
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Wet dressings | Application of wet dressings in combination with topical corticosteroids helps with skin barrier recovery, as it increases the efficacy of the corticosteroid and protects the skin from persistent scratching. Overuse of wet dressings can cause skin maceration, folliculitis and secondary skin infections. |
Phototherapy | Most commonly used phototherapy modality is narrow-band UVB. Photochemotherapy with PUVA should be restricted to patients with severe widespread eczema.Broadband UVB, and UVA1 where available may also be useful. |
Systemic immunomodulatory agents | Methotrexate, ciclosporin, mycophenolate mofetil, azathioprine, interferon-gamma and systemic corticosteroids have shown to provide benefit for patients with severe refractory eczema.Use is limited by their potentially serious adverse effects. |
Hospitalisation | Patient is removed from environmental allergens, irritants, and stressors.Patient education and compliance with therapy are intensified. |
Allergen immunotherapy | Possible consideration in selected eczema patients with associated aeroallergen sensitivity. |
Referral for specialist advice | |
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Referral for inpatient care | Eczema herpeticum is suspectedEczema is severe and not responding to treatment Bacterially infected eczema is not responding to appropriate treatmentFor education, support and respite in select cases |
Referral for eczema nurse advice | Where the patient and caregivers would benefit from advice and support regarding correct use of treatment |
Referral for specialist dermatologist advice | The diagnosis is uncertain Eczema on the face has not responded to treatmentContact dermatitis is suspected Eczema is causing significant psychological or social problems Eczema is associated with severe or recurrent infections The family or child would benefit from specialist advice on treatment Where phototherapy or systemic treatment is required |
Referral for psychological advice | Children with ongoing psychological or social impact despite appropriate medical advice |
Referral for specialist paediatric advice | Children with suspected immediate food hypersensitivity Children with poor growth Children with severely restricted diets |
Differential diagnosis of atopic dermatitis:
Seborrheic Dermatitis: Pathophysiology: Overactive sebaceous glands, Malassezia yeast overgrowth. Symptoms: Scalp: dandruff; Face: erythema, scales. Associated Conditions: Linked to neurological disorders (e.g., Parkinson’s). Management: Antifungal shampoos, topical steroids for inflammation. |
Psoriasis: Pathophysiology: Immune-mediated, genetic predisposition. Comorbidities: Increased risk of arthritis, cardiovascular diseases. Treatment: Topical corticosteroids, phototherapy, systemic medications. |
Nummular Dermatitis: Etiology: Allergic reaction, dry skin, stress. Symptoms: Itchy, coin-shaped lesions; Crusting and oozing. Treatment: Emollients, topical steroids, antihistamines. |
Contact Dermatitis: Allergic Type Mechanism: Sensitization after initial exposure. Irritant Type Mechanism: Direct damage to the skin barrier. Management Approaches: Recognition relies on temporal patterns and suggestive distribution. Allergic CD may manifest as autoeczematization, with widespread, symmetrically distributed lesions. Strict avoidance of triggers is the most effective approach. Topical corticosteroids (TCS) or topical calcineurin inhibitors (TCIs) can reduce inflammation when triggers cannot be avoided. Chronic use of TCS, especially on the face and diaper area, should be avoided due to the risk of skin barrier compromise. |
Pityriasis Alba: Pathophysiology: Common, idiopathic, asymptomatic condition associated with AD. Associated Conditions: Considered a minor diagnostic criterion for AD. Comorbidities: Most often found in school-age children with no gender bias. Management Approaches: Emollients can minimize scaling, but hypopigmentation may persist for months to years despite control of xerosis and inflammation. Some reports suggest efficacy of TCIs. |
Overlap: Psoriasis-eczema overlap Clinical Challenge: Diagnosis and management may be complex. Treatment Approach: Address both eczematous and psoriatic features. |
Dermatographism: Pathophysiology: Immunologic response to pressure on the skin. Associated Conditions: Idiopathic in most cases but can be associated with drug reactions, scabies, stress/anxiety, or systemic diseases (e.g., hyperthyroidism, type 2 diabetes mellitus). Comorbidities: Usually diagnosed in young adults, gradual onset, resolution often within five years. Management Approaches: Trigger avoidance is the most effective way to control dermatographism. |
Bacterial Infections Impetigo: Pathophysiology: Superficial bacterial infection often caused by S. aureus or Streptococcus pyogenes. Clinical Features: Erythema, edema, tenderness, honey-yellow crusting. Management: Skin cleansing, topical antibiotics, dilute bleach baths, oral antibiotics for widespread disease or fever. Secondary Syphilis: Presentation: Widespread eruption weeks to months after primary chancre. Can involve various skin surfaces. Symptoms: Fever, lymphadenopathy, mucosal ulceration, condyloma latum. Note: Rare due to antibiotics; more common in congenital cases. |
Viral Infections Molluscum Dermatitis: Characteristics: Benign infection causing flesh-colored papules; some develop dermatitis (MD). Association: More severe in patients with AD; no conclusive link to MC susceptibility. Management: Uncomplicated MC usually requires no treatment; MD may benefit from short-course TCS. Eczema Herpeticum: Pathophysiology: Life-threatening viral infection by herpes simplex virus, mainly in patients with chronic skin disease (especially AD). Presentation: Widespread tender erosions, face predilection; may be mistaken for impetigo. Treatment: Empiric antiviral treatment; monitoring due to recurrence risk. Eczema Vaccinatum: Occurrence: Rare, potentially life-threatening eruption after smallpox vaccination. Risk Factors: Atopy, primary skin disease with barrier dysfunction, primary immunodeficiency. Presentation: Generalized vesiculopustular eruption. Eczema Coxsackium: Variant: Associated with coxsackievirus A6. Characteristics: EH-like lesions, fever, constitutional symptoms, onychomadesis. Association: More common in children with AD. Diagnosis: Confirmed by serum PCR for coxsackievirus. Viral Exanthem: Characteristics: Heterogeneous group associated with various systemic viral infections. Common VE: Acute onset of generalized morbilliform eruption. Management: Generally self-limited; supportive treatment. |
Fungal Infections Tinea (Ringworm): Appearance: Annular, red, scaly patches with central clearing. Types: Tinea corporis, faciei, capitis; systemic antifungal needed for tinea capitis. Note: AD patients prone to tinea; misdiagnosed as AD may lead to “tinea incognito.” Candidiasis: Occurrence: Uncommon widespread infection, more frequent in infants; localized in skin folds in adults. Types: Congenital and neonatal in infants; localized to skin folds in adults. Presentation: Erythroderma, desquamation, proximal nail dystrophy. |
Infestations – Scabies: Pathophysiology: Allergic reaction to Sarcoptes scabei. Presentation: Red papulovesicles, dermatitic lesions; intense pruritus. Diagnosis: Linear burrows, positive scrapings. Note: AD patients more prone; TCS use may mask symptoms (“scabies incognito”). |
Genetic Disorders: Keratosis Pilaris (KP): Chicken Skin – Follicular keratinization disorder. typically seen in children and young adults. It affects 50–70% of teenagers and 40% of adults. Ichthyoses: excessive dry, scaly skin The name “ichthyosis“ is derived from the Greek root “ichythys” meaning fish, to which ichthyosis vulgaris owes its other names, “fish scale disease,” or “fish skin disease”; “vulgaris” means common. Usually not present at birth. Most often it appears after about 2 months and in most cases before the age of 5. Symptoms may worsen up to puberty, and sometimes improve with age. Treatments: keep the skin hydrated – Apply emollients with high lipid content, such as lanolin cream reduce scale – Bathe in salt water, Apply creams or lotions containing salicylic acid, glycolic acid, lactic acid or urea to exfoliate and moisturise skin. Oral retinoids such as acitretin or isotretinoin can be prescribed in severe cases. |
Immunodeficiency Disorders: Netherton Syndrome: Defect in the SPINK5 gene. HIV/AIDS-Related Skin Changes: Opportunistic infections, Kaposi’s sarcoma. |
Drug Eruptions: Most common rashes managed by physicians. Manifestations: Types: Erythema, urticaria, erythema multiforme (EH-like reaction), fixed drug eruption. Appearance: Erythematous lesions (maculopapular or morbilliform), urticaria (papules to annular plaques), fixed drug eruptions (solitary or multiple, recurring in the same location). Distribution: Lesions often begin on the trunk and symmetrically distributed. Diagnosis Approach: Relies on medical history, clinical examination, and may involve skin biopsy if needed. Treatment – Cessation: Primary step involves discontinuation of the causative drug, if possible. Supportive Care: Supportive treatment with emphasis on managing dermatitis using topical corticosteroids (TCS). |
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