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Questions and Answers
Which characteristic is most commonly associated with Atopic Dermatitis in infants?
Which characteristic is most commonly associated with Atopic Dermatitis in infants?
What is a primary treatment goal for Atopic Dermatitis?
What is a primary treatment goal for Atopic Dermatitis?
Which of the following best describes the epidemiology of Atopic Dermatitis?
Which of the following best describes the epidemiology of Atopic Dermatitis?
Which change in the skin is NOT associated with epidermal barrier dysfunction in Atopic Dermatitis?
Which change in the skin is NOT associated with epidermal barrier dysfunction in Atopic Dermatitis?
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What percentage of infants and young children with Atopic Dermatitis are likely to go into remission by age 12?
What percentage of infants and young children with Atopic Dermatitis are likely to go into remission by age 12?
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Which of the following is true regarding late-onset Atopic Dermatitis?
Which of the following is true regarding late-onset Atopic Dermatitis?
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What is the function of fillagrin in the skin?
What is the function of fillagrin in the skin?
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What is one factor that can predispose individuals with Atopic Dermatitis to skin infections?
What is one factor that can predispose individuals with Atopic Dermatitis to skin infections?
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Which option best describes the alteration of the cutaneous microbiome in Atopic Dermatitis?
Which option best describes the alteration of the cutaneous microbiome in Atopic Dermatitis?
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Which demographic is less likely to develop IgE antibodies associated with Late-onset Atopic Dermatitis?
Which demographic is less likely to develop IgE antibodies associated with Late-onset Atopic Dermatitis?
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What role do Stratum Corneum lipids play in epidermal function?
What role do Stratum Corneum lipids play in epidermal function?
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What pathological change in the cutaneous microbiome is associated with atopic dermatitis (AD)?
What pathological change in the cutaneous microbiome is associated with atopic dermatitis (AD)?
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Which immune response regulation is implicated in the development of AD?
Which immune response regulation is implicated in the development of AD?
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Which histological characteristic is typical of an acute atopic dermatitis lesion?
Which histological characteristic is typical of an acute atopic dermatitis lesion?
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In which age group does atopic dermatitis commonly present with severe excoriations and chronic skin lesions due to scratching?
In which age group does atopic dermatitis commonly present with severe excoriations and chronic skin lesions due to scratching?
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What clinical feature is most typical of childhood atopic dermatitis?
What clinical feature is most typical of childhood atopic dermatitis?
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What is a common feature of atopic dermatitis lesions in the elderly?
What is a common feature of atopic dermatitis lesions in the elderly?
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Which factor is least likely to lead to increased stratum corneum permeability?
Which factor is least likely to lead to increased stratum corneum permeability?
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What is the primary feature of atopic dermatitis in infants?
What is the primary feature of atopic dermatitis in infants?
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Which of the following is NOT a typical site for eczema in childhood atopic dermatitis?
Which of the following is NOT a typical site for eczema in childhood atopic dermatitis?
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What is the primary mechanism through which fillagrin mutations affect Atopic Dermatitis severity?
What is the primary mechanism through which fillagrin mutations affect Atopic Dermatitis severity?
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Which age group is typically characterized by a shift from acute inflammation to chronic inflammation in Atopic Dermatitis?
Which age group is typically characterized by a shift from acute inflammation to chronic inflammation in Atopic Dermatitis?
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What feature distinguishes late-onset Atopic Dermatitis from early-onset?
What feature distinguishes late-onset Atopic Dermatitis from early-onset?
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How does the alteration of the cutaneous microbiome relate to Atopic Dermatitis?
How does the alteration of the cutaneous microbiome relate to Atopic Dermatitis?
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Which of the following factors is NOT considered a common triggering factor for Atopic Dermatitis?
Which of the following factors is NOT considered a common triggering factor for Atopic Dermatitis?
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In the context of Atopic Dermatitis pathogenesis, what does immune dysregulation most commonly involve?
In the context of Atopic Dermatitis pathogenesis, what does immune dysregulation most commonly involve?
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What demographic is most commonly affected by late-onset Atopic Dermatitis?
What demographic is most commonly affected by late-onset Atopic Dermatitis?
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Which of the following is a direct consequence of epidermal barrier dysfunction in Atopic Dermatitis?
Which of the following is a direct consequence of epidermal barrier dysfunction in Atopic Dermatitis?
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What is a common feature of Atopic Dermatitis lesions in elderly patients?
What is a common feature of Atopic Dermatitis lesions in elderly patients?
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Which of the following statements about the treatment goals for Atopic Dermatitis is incorrect?
Which of the following statements about the treatment goals for Atopic Dermatitis is incorrect?
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What is the primary consequence of elevated levels of endogenous proteases in atopic dermatitis?
What is the primary consequence of elevated levels of endogenous proteases in atopic dermatitis?
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In the clinical presentation of atopic dermatitis in childhood, which characteristic is likely to be observed?
In the clinical presentation of atopic dermatitis in childhood, which characteristic is likely to be observed?
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Which aspect of cutaneous microbiome alteration is most relevant to atopic dermatitis?
Which aspect of cutaneous microbiome alteration is most relevant to atopic dermatitis?
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What characteristic histological feature is primarily associated with acute lesions of atopic dermatitis?
What characteristic histological feature is primarily associated with acute lesions of atopic dermatitis?
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In elderly patients with atopic dermatitis, which feature is typically noted?
In elderly patients with atopic dermatitis, which feature is typically noted?
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How does the immune dysregulation contribute to atopic dermatitis?
How does the immune dysregulation contribute to atopic dermatitis?
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What is the typical skin manifestation of atopic dermatitis in infants aged 2 months to 2 years?
What is the typical skin manifestation of atopic dermatitis in infants aged 2 months to 2 years?
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What type of lesions are typical in adult/adolescent presentations of atopic dermatitis?
What type of lesions are typical in adult/adolescent presentations of atopic dermatitis?
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Which of the following factors does NOT contribute to the permeability barrier dysfunction in atopic dermatitis?
Which of the following factors does NOT contribute to the permeability barrier dysfunction in atopic dermatitis?
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What chronic condition can develop from continuous scratching in patients with childhood atopic dermatitis?
What chronic condition can develop from continuous scratching in patients with childhood atopic dermatitis?
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Study Notes
Atopic Dermatitis (AD)
- AD is a common inflammatory skin condition, frequently beginning in infancy or early childhood.
- It often co-occurs with other atopic disorders like asthma, allergic rhinitis, and food allergies.
- AD is a complex genetic condition influenced by environmental factors.
- Key features include intense itching (pruritus) and a chronic, relapsing course.
- In infants, the cheeks, scalp, and extensor surfaces are predominantly affected; in children and adults, flexor regions are more affected.
- AD can predispose individuals to skin infections with Staphylococcus aureus and herpes simplex virus (HSV).
- The incidence of AD peaks in infancy and often progresses to a chronic disease.
- AD has three subsets: early-onset, late-onset, and elderly-onset.
- Early-onset AD usually occurs in the first two years of life and is the most common type.
- Approximately half of children develop allergen-specific IgE antibodies before age two.
- Approximately 60% of infants and young children with AD go into remission by age 12.
- Late-onset AD starts after puberty, and 30% of late-onset patients don't develop IgE antibodies.
- A subset of AD appears in older adults (over 60).
Treatment Goals for AD
- Avoiding triggers is crucial.
- Regular use of emollients (moisturizers) is essential.
- Anti-inflammatory therapies are used to manage both subclinical and overt flare-ups.
Epidemiology of AD
- AD frequently manifests in infancy and has a chronic disease course.
- Early-onset AD usually appears in the first two years of life and is the most common type.
- Approximately half of children develop allergen-specific IgE antibodies before age two.
- Approximately 60% of infants and young children with AD go into remission by age 12.
- Late-onset AD starts after puberty, and 30% of late-onset patients don't develop IgE antibodies.
- A subset of AD appears in older adults (over 60).
Pathogenesis of AD
- Epidermal barrier dysfunction is a key component, with impaired stratum corneum (SC) barrier function, including filaggrin and other genetic barrier protein deficiencies.
- Immune dysregulation contributes to the inflammatory response, including keratinocyte-derived pro-Th2 and pro-innate lymphoid cell (ILC) cytokines.
- Alterations in the cutaneous microbiome are implicated, with bacteria (S. aureus), fungi (Malassezia), and viruses (HSV) contributing to inflammation.
Manifestations of Epidermal Barrier Dysfunction
- Increased transepidermal water loss (TEWL).
- Changes in skin pH.
- Increased skin permeability.
- Changes in skin protein and lipid composition, notably filaggrin.
- Mutations in filaggrin are associated with early-onset and increased severity of AD.
- Critical stratum corneum (SC) lipids are vital for barrier function. Any abnormalities increase epidermal permeability.
- Elevated endogenous protease levels lead to corneocyte dysadhesion.
Immune Dysregulation and Cutaneous Microbiome
- Imbalance in both innate and adaptive immunity leads to inflammatory mediator release.
- Key microbes in the cutaneous microbiome homeostasis include bacteria (S. aureus), fungi (Malassezia), and viruses (HSV).
- Environmental changes in these microbes can induce AD.
- Irritants, microbes, and allergens trigger immune responses, leading to AD inflammatory mediator and cytokine release.
Clinical Features of AD
- AD displays a wide spectrum of clinical features varying by age.
- Acute, subacute, and chronic eczematous lesions exhibit intense itching.
- Infantile AD (2 months to 2 years): edematous papules and papulovesicles primarily on the cheeks, extending to the scalp and neck.
- Childhood AD (2 to 12 years): less exudative, xerotic, or lichenified lesions, primarily on flexural areas (ankles, elbows).
- Adult/adolescent AD (over 12 years): hand dermatitis, intense flexural involvement, potential for severe excoriations.
- Elderly AD (over 60 years): lichenified flexural lesions, often with marked xerosis (dryness).
Differential Diagnosis
- AD can be misdiagnosed.
- Chronic dermatoses (seborrheic dermatitis, contact dermatitis, psoriasis, nummular eczema).
- Infections and infestations (scabies, dermatophytosis).
- Primary immunodeficiencies.
- Malignancies (mycosis fungoides, Sézary syndrome).
- Metabolic or Genetic conditions (Netherton syndrome, ectodermal dysplasia).
- Autoimmune disorders (dermatitis herpetiformis, pemphigus foliaceus).
Treatment of AD
- General Approach: Education, trigger avoidance, maintaining skin hydration.
- Bathing: Short, lukewarm baths with fragrance-free, non-soap cleansers, followed by emollients.
- Moisturizers: Daily use to reduce TEWL, itching, and inflammation.
- Topical Therapy: Corticosteroids, calcineurin inhibitors, topical JAK inhibitors, wet wrap therapy.
- Systemic Therapy: Corticosteroids, JAK inhibitors (e.g., dupilumab), adjunctive therapies (antimicrobials).
- Phototherapy: NB-UVB, UVA.
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Description
This quiz provides a comprehensive overview of atopic dermatitis (AD), including its characteristics, co-occurring conditions, treatment goals, and epidemiology. Explore the complexities of this common skin condition, influencing factors, and management strategies to better understand AD.