Teaching Clinic: Common Dermatoses Flashcards

1
Q

Clinical assessment of Skin

A
  1. Morphology + Distribution
    - Colour
    - Shape
    - Border
    - Surface
    - Pattern: linear, annular, grouped, reticular
  2. Inspection + Palpate
  3. Type of lesion
    - Primary lesions: macule, patch, papule, nodule, plaque, pustule, vesicle, bulla, blister, wheal, telangiectasia etc.
    - Secondary lesions: crust, excoriation, lichenification, scar, scaling, exfoliation, fissure, erosion, ulcer, atrophy etc.
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2
Q

Urticaria vs Angioedema

A

Both involve the same edematous process, but at different levels of the cutaneous vascular plexus

Urticaria:
- Composed of wheals (transient edematous papules and plaques), usually pruritic, due to edema of papillary body)

  1. Acute
    - Acute onset, lasts **<6 weeks
    - Often **
    IgE-dependent with atopy (e.g. triggered by parasites, drugs, alimentary agents)
    - Can be complement-mediated (e.g. serum-sickness like reaction)
    - Common: Infection-related
  2. Chronic
    - Lasts ***>6 weeks
    - Rarely IgE-dependent
    - Mostly “idiopathic”

DDx:
1. **Urticarial vasculitis
2. **
Drug eruption
3. **Viral exanthem
4. Bites / Papular urticaria
5. **
Bullous pemphigoid

Treatment:
1. Discontinue suspected triggers
2. Anti-histamines: Sedative / Non-sedative
3. Immunosuppressants
- Corticosteroid (Topical steroids: not generally effective)
- Cyclosporine, Azathioprine
4. Biologic: Anti-IgE (Omalizumab)

Angioedema:
- Larger edematous area that involves dermis & subcutaneous tissue
- Deep, ill-defined

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3
Q

Atopic eczema

A
  • Chronic relapsing pruritic exanthematous dermatosis
  • Characterised primarily by an **allergic diathesis, **erythema, oozing, crusting, excoriations, lichenification and dehydration of involved skin

Established criteria for diagnosis:
1. Hanifin + Rajka’s criteria (3 major + 3 minor criteria)
2. 1994 UK Working Party’s diagnostic criteria (pruritus and 3 of flexural involvement, asthma / hayfever, generalized dry skin, onset under 2 year old)

Distribution: **Age-dependent
- Infant: **
extensor surfaces of limbs, face, neck, scalp, trunk
- Child: **flexures, trunk
- Adolescent: neck, face, **
extensor surfaces of upper and lower limbs, breasts, hands

Morphology:
- Ill-defined border, symmetrical
- Acute / Subacute / Chronic

Complications:
- Secondary infections e.g. Impetigo, Cellulitis

DDx:
- **Seborrhoeic dermatitis
- **
Contact dermatitis
- ***Psoriasis
- Scabies

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4
Q

Contact dermatitis

A
  1. Contact Irritant Dermatitis
    - inflammatory reaction in the skin resulting from exposure to a substance that causes an eruption in most people who come in contact with it
  2. Contact Allergic Dermatitis
    - **acquired sensitivity to various substances that produce inflammatory reactions in those, and only those, who have previously been **sensitised to the allergen

Patch test:
- Intact, uninflamed skin
- Upper back
- Non irritating concentration of suspected substances / allergens
- Patches removed after 48 hours
- Assess for reaction at 48 hours and at 96 hours
- Erythematous papules, vesicles, oedema
- “Excited skin syndrome”: state of hyper-irritability. Negative tests may appear as weakly positive

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5
Q

Psoriasis

A

Classification:
1. **Psoriasis vulgaris
- Chronic plaque psoriasis
- Guttate psoriasis
- Inverse psoriasis
- Palmoplantar psoriasis
2. **
Erythrodermic psoriasis
3. ***Pustular psoriasis
- Von Zumbusch’s disease
- Palmoplantar pustulosis
- Acrodermatitis continua

Clinical features:
1. **Chronic large plaque
2. **
Guttate
3. **Pustular
4. **
Erythoderma
5. **Nail
- Pitting
- Onycholysis
- Subungual hyperkeratosis
- Oil-drop sign
- Nail dystrophy
6. **
Scalp / Joints
7. **Auspitz sign (small bleeding points after successive layers of scale have been removed from the surface of psoriatic papules or plaques)
8. **
Koebner phenomenon (appearance of new skin lesions on previously unaffected skin secondary to trauma)

Management principles depend on:
1. Age
2. Type of psoriasis
3. Site, extent of involvement
4. Previous treatments
5. Associated medical disorders
6. Lifestyle of patients

Treatment:
1. Topical
- Emollient
- **Corticosteroid
- **
Vitamin D analogue
- ***Coal tar
- Tazarotene

  1. ***Phototherapy
    - NBUVB, PUVA
  2. Systemic treatment
    - Methotrexate
    - ***Retinoids
    - Cyclosporine
  3. Biologics
    - Anti-TNF (Infliximab, Etanacept, Adalimumab)
    - Anti-IL12/23 (Utekinumab)
    - Anti-IL17 (Secukinumab)
    - JAK inhibitor (Tofacitinib)
    - PDE-4 inhibitor (Apremilast)
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6
Q

Impetigo

A

Causative organisms:
- **Staphylococcus / **Streptococcus

Clinical features:
- **Vesicles / **Pustules that arise on **erythematous base with **crusting formation
- In skin damaged by previous minor trauma such as scratching / insect bite

DDx:
- Discoid eczema
- Herpes simplex
- Varicella

Treatment:
1. Topical / Systemic antibiotics
- ***Cloxacillin, Cefuroxime, Erythromycin

Complication:
- ***Post-infective glomerulonephritis

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7
Q

Dermatophytic infection

A
  1. Tinea unguium / Onychomycosis (nail)
  2. Tinea pedis (feet)
  3. Tinea cruris (groin)
  4. Tinea corporis (trunk)
  5. Tinea manuum (hands)
  6. Tinea capitis (scalp)
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8
Q

Viral warts

A

Causative organism:
- ***Human Papilloma Virus (HPV)
- Transmitted by contact
- Genital wart: sexually transmitted

Clinical features:
- Warty lesions with blood vessels beneath surface
- Painful in sole
- Genital wart can be associated with ***neoplastic changes (e.g. SCC in-situ, SCC)

Treatment:
1. **Salicylic acid
2. **
Cryotherapy + Cauterization
3. ***Topical 5% imiqimod

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9
Q

Herpes zoster

A
  • Reactivation of latent VZV
  • Usually elderly

Clinical features:
- **Dermatomal distribution
- **
Painful erythematous eruption followed by **Vesicle + Pustules formation that clustered into a **herpetiform arrangement
- Affect ***eye If involve Trigeminal nerve

Complications in immune competent patients:
1. Peripheral nerve palsies
2. Encephalitis
3. Myelitis
4. Contralateral hemiparesis

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10
Q

Acne vulgaris

A
  • Common in teenage (80%)
  • M>F
  • Positive Family history
  • Often neglected: asymptomatic, not life-threatening
  • Some patients / parents considered acne to be “normal” for puberty

Pathogenesis:
1. Seborrhoea
- **Excessive sebum production due to over-response to **androgens or excessive androgen secretion
2. **Comedogenesis
- Hypercornification of pilosebaceous ducts
3. Infection
- **
Propionibacterium acnes (P. acnes)
4. Inflammation
- **Lipolysis of sebum of P. acnes
- Superantigen from P.acnes triggers **
inflammation of comedones
- Inflammatory mediators from ductal corneocytes

Clinical features:
1. Comedones
- Open / Closed
- Non-inflamed
2. Papules, pustules
- Superficial inflamed lesions
3. Nodules, cysts
- Deep inflamed lesions

Treatment:
1. Topical therapy
- **Retinoids
- **
Benzoyl peroxide
- **Azelaic acid
- **
Antibiotics
2. Oral therapy
- Antibiotics
- OC pills
- **Isotretinoin (Roaccutane): Stop contraception **1 month after completion of isotretinoin

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