Master Dermatology
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Core Concepts
The skin comprises three layers: epidermis (keratinocytes, melanocytes, Langerhans, Merkel cells), dermis (collagen, elastin, blood vessels, nerves, adnexal structures), and subcutaneous tissue. Understanding primary (macule, papule, plaque, nodule, vesicle, bulla, pustule, wheal, patch) and secondary lesions (erosion, ulcer, crust, scale, lichenification, atrophy, scar) is fundamental for description and diagnosis. Key symptoms include pruritus (itch), pain, and altered sensation. Systemic diseases often manifest cutaneously (e.g., lupus, diabetes, IBD, internal malignancy).
Clinical Presentation
- Eczema (Dermatitis):
- Atopic: Pruritic, erythematous, scaly patches, often lichenified. Flexural distribution (children), extensor (infants). Associated with asthma, hayfever.
- Contact: Allergic (delayed hypersensitivity, e.g., nickel) or irritant (e.g., detergents). Erythema, vesicles, pruritus, localized to exposure.
- Seborrheic: Greasy yellow scales on erythematous patches, typically face (nasolabial folds, eyebrows), scalp ("cradle cap" in infants). Often exacerbated by stress, Parkinson's, HIV.
- Discoid (Nummular): Coin-shaped erythematous, vesicular, and crusted plaques, intensely pruritic. Lower legs/arms.
- Psoriasis: Chronic inflammatory. Well-demarcated erythematous plaques with silvery scales. Extensor surfaces, scalp, nails (pitting, onycholysis, subungual hyperkeratosis). Auspitz sign (pinpoint bleeding after scale removal).
- Variants: Plaque (most common), Guttate (post-strep infection), Pustular (generalized/localized, acute fever), Erythrodermic (total body erythema, emergency).
- Associated with Psoriatic Arthritis, metabolic syndrome, CVD.
- Urticaria (Hives): Transient, intensely pruritic wheals (erythematous, edematous papules/plaques) with surrounding flare. Acute (<6 weeks), Chronic (>6 weeks). Can be associated with angioedema. Causes: allergic (food, drugs), physical, autoimmune, idiopathic.
- Infections:
- Bacterial: Impetigo (honey-crusted lesions, Staph/Strep), Cellulitis (erythema, warmth, swelling, pain, poorly demarcated, deeper dermis), Erysipelas (Strep, sharply demarcated, raised border, superficial dermis).
- Fungal (Tinea): Ringworm (annular, scaly plaques with central clearing). Tinea pedis (athlete's foot), corporis (body), cruris (groin), capitis (scalp, can cause alopecia), unguium (onychomycosis, nail dystrophy).
- Viral: Herpes Simplex (vesicles on erythematous base, grouped), Herpes Zoster (dermatomal vesicles, painful, unilateral), Warts (HPV), Molluscum Contagiosum (umbilicated papules).
- Blistering Disorders:
- Bullous Pemphigoid: Subepidermal blisters (tense), older adults, often itchy, negative Nikolsky's sign.
- Pemphigus Vulgaris: Intraepidermal blisters (flaccid), younger adults, often mucosal involvement, positive Nikolsky's sign.
- Drug Reactions: Morbilliform (maculopapular, most common), Urticarial, Fixed drug eruption, Erythema Multiforme (target lesions), SJS/TEN (severe, mucosal involvement, epidermal detachment).
- Skin Cancers:
- Basal Cell Carcinoma (BCC): Pearly papule with telangiectasias, rolled border, often central ulceration. Most common skin cancer, rarely metastasizes.
- Squamous Cell Carcinoma (SCC): Keratotic, crusted, nodular lesion, often ulcerated. Sun-exposed areas. Can metastasize. Precursor: Actinic Keratosis.
- Melanoma: ABCDE criteria (Asymmetry, Border irregularity, Colour variability, Diameter >6mm, Evolving/Elevated). Highly metastatic.
Diagnosis (Gold Standard)
Clinical examination is paramount. For uncertain lesions, a skin biopsy (punch, shave, excisional) for histopathology provides definitive diagnosis (e.g., tumors, inflammatory dermatoses, blistering disorders). Direct immunofluorescence (DIF) on perilesional skin for blistering diseases. Dermatoscopy for pigmented lesions. KOH mount of skin scrapings for fungal infections. Patch testing for allergic contact dermatitis. Bacterial/viral swabs for culture/PCR.
Management (First Line)
Management often involves:
- Topical Steroids: Key for inflammatory conditions (eczema, psoriasis). Potency adjusted based on site, severity, and age.
- Emollients: Essential for dry skin conditions (eczema, psoriasis) to restore barrier function.
- Antihistamines: Oral H1-blockers for pruritus (urticaria, eczema).
- Antifungals: Topical (clotrimazole, terbinafine) or oral (terbinafine, fluconazole) depending on extent and site.
- Antibiotics: Topical (fusidic acid, mupirocin) or oral (flucloxacillin, erythromycin) for bacterial infections.
- Antivirals: Oral acyclovir/valacyclovir for herpes simplex/zoster.
- Immunosuppressants/Biologics: For severe chronic conditions (e.g., methotrexate, ciclosporin, biologics for psoriasis/atopic dermatitis).
- Phototherapy: UVB or PUVA for extensive psoriasis/eczema.
- Surgery: Excision for skin cancers (BCC, SCC, melanoma). Cryotherapy for actinic keratosis, warts.
- Drug Discontinuation: Immediate cessation of causative drug for drug eruptions (especially SJS/TEN).
Exam Red Flags
- SJS/TEN: Widespread painful erythema, bullae, mucosal involvement (>2 sites), epidermal detachment (>10% SJS, >30% TEN). Medical emergency, often drug-induced.
- Erythroderma: >90% body surface erythema and scaling. Risk of hypothermia, fluid loss, high-output cardiac failure. Can be due to severe psoriasis, eczema, drug reaction, lymphoma.
- Necrotizing Fasciitis: Rapidly spreading infection, severe pain out of proportion to exam, crepitus, systemic toxicity, skin necrosis. Surgical emergency.
- Generalized Pustular Psoriasis: Acute onset of widespread pustules, fever, systemic upset. Requires urgent treatment to prevent complications.
- Melanoma (Evolving Lesion): Any rapidly changing pigmented lesion, especially with ABCDE features. Early recognition is crucial for prognosis.
- Dermatological Manifestations of Systemic Disease: Be aware of associations (e.g., lupus rash, dermatomyositis, vasculitis, xanthomas in dyslipidaemia, acanthosis nigricans in insulin resistance/malignancy).
Sample Practice Questions
A 35-year-old man presents with a 6-month history of intensely itchy, red, scaly patches on his elbows, knees, and scalp. The patches are well-demarcated and covered with silvery-white scales. He also reports pitting and onycholysis of his fingernails. He has no other significant medical history.
A 32-year-old man presents to the emergency department with a sudden onset, intensely itchy rash and swelling of his lips and eyelids. The skin lesions are raised, erythematous weals that are migratory, appearing and disappearing within a few hours, but new ones keep forming. He reports no difficulty breathing or swallowing. He has no known allergies and has not started any new medications. His vital signs are stable. Physical examination confirms widespread erythematous weals and angioedema of the lips and eyelids. The lesions blanch with pressure and resolve within 24 hours.
A 72-year-old woman presents with a 3-day history of burning pain and a vesicular rash distributed across her left chest wall, stopping abruptly at the midline. She describes the pain as severe and reports feeling tired and feverish. She has a history of chickenpox in childhood.
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