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Dermatological Examination

Dermatological Examination

Dermatological Examination

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Exam Essentials - Gear Up & Gaze

  • Lighting: Optimal: natural daylight. Wood's lamp for specific fluorescence (e.g., fungal, pigmentary).
  • Essential Gear: Magnifying lens (handheld, 10-20x), dermatoscope, glass slide (for diascopy), flexible ruler, gloves, camera.
  • Initial Gaze:
    • Assess patient's general health.
    • Note skin phototype (Fitzpatrick I-VI).
    • Observe lesion distribution (e.g., acral, flexural) & overall pattern.

⭐ Diascopy is crucial: distinguishes vascular erythema (blanches) from purpura/telangiectasia (non-blanching).

History Hints - Patient Puzzles

  • Onset & Duration: Acute, chronic, recurrent?
  • Pruritus: Timing, severity. Associated pain/burning?
  • Lesion Evolution: Initial site, spread, changes (color, texture).
  • Triggers: Sun, heat, stress, drugs, allergens.
  • Past Hx: Atopy (eczema, asthma), prior skin issues.
  • Drug Hx: All current/recent (Rx, OTC, herbal).
  • Family Hx: Psoriasis, atopy.
  • Occupation/Travel: Exposures, recent trips.
  • Systemic: Fever, weight loss, arthralgia.

⭐ Drug history is key; eruptions mimic many dermatoses. Note all new medications.

Primary Lesions - Spot Spectrum

  • Flat, non-palpable lesions; color change only.
  • Macule:
    • Circumscribed, < 1 cm in diameter.
    • Color change, no elevation/depression.
    • E.g., Freckles, lentigines, junctional nevi, tinea versicolor.
  • Patch:
    • A macule > 1 cm in diameter.
    • Flat, non-palpable, color change.
    • E.g., Café-au-lait spot, vitiligo, port-wine stain, mongolian spot.
  • 📌 Macule = Mini (<1cm); Patch = Plainly Prominent (>1cm).

⭐ > The key differentiator between a macule and a patch is size (<1cm vs >1cm); both are primary, flat, non-palpable lesions representing a color alteration.

Secondary Signs - Evolution Evidence

  • Scales: Shedding epidermal flakes (e.g., psoriasis, tinea).
  • Crusts: Dried exudate; honey-colored (impetigo), hemorrhagic, serous.
  • Erosions: Superficial epidermal loss; heals without scarring.
  • Ulcers: Deeper dermal/subcutaneous loss; heals with scarring.
  • Fissures: Linear skin cracks (e.g., hand eczema, angular cheilitis).
  • Atrophy: Skin thinning; epidermal, dermal, or subcutaneous.
  • Lichenification: Thickened skin, exaggerated markings from chronic rubbing.
  • Excoriations: Scratch marks, often linear, self-induced.
  • Scars: Post-injury fibrous tissue; hypertrophic, atrophic. Secondary skin lesion morphologies

⭐ Lichenification is a hallmark of chronic rubbing or scratching, classically seen in conditions like atopic dermatitis or lichen simplex chronicus, indicating chronicity of the lesion.

Patterns & Probes - Clue Clusters

  • Distribution Clues:
    • Symmetrical: Eczema, Psoriasis.
    • Flexural: Atopic dermatitis; Extensor: Psoriasis.
    • Photosensitive: SLE; Dermatomal: Herpes Zoster.
    • Koebner phenomenon: Psoriasis, Lichen Planus, Vitiligo.
  • Configuration Clues:
    • Annular: Tinea corporis, Granuloma annulare.
    • Linear: Lichen striatus, Koebner.
    • Grouped (Herpetiform): Herpes simplex/zoster.
    • Targetoid: Erythema multiforme.
  • Diagnostic Probes:
    • Diascopy: Differentiates vascular (blanchable) from hemorrhagic.
    • Dermoscopy: Magnified view of structures, patterns.
    • Wood's Lamp: Detects fluorescence (e.g., Microsporum).

Dermatological lesion distribution patterns

⭐ > The Koebner phenomenon (isomorphic response) refers to the appearance of new skin lesions on previously unaffected skin secondary to trauma; classically seen in psoriasis, lichen planus, and vitiligo.

High‑Yield Points - ⚡ Biggest Takeaways

  • Inspection is paramount: note lesion morphology (type, shape, arrangement, distribution) and color.
  • Palpation evaluates texture, consistency, tenderness, temperature, and mobility of lesions.
  • Diascopy distinguishes blanchable erythema (vascular) from non-blanchable purpura (hemorrhagic).
  • Wood's lamp examination detects specific fungal/bacterial infections and pigmentary anomalies.
  • Dermoscopy visualizes subsurface skin structures, improving diagnosis of pigmented/non-pigmented lesions.
  • Skin biopsy (punch, shave, excisional) is vital for histopathological diagnosis in uncertain cases.
  • Always conduct a thorough skin examination, including mucous membranes, hair, and nails.

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