MRCP Dermatology Preparation Strategy
Focus your preparation on British Association of Dermatologists (BAD) guidelines, as these represent the authoritative, evidence-based resources most relevant to MRCP dermatology content. 1
Core Resource Framework
Primary Resources
- BAD guidelines are your foundation - these are NHS Evidence-accredited and follow rigorous AGREE methodology for guideline development 1
- BAD guidelines provide strength of recommendations (A-E) and quality of evidence ratings (I-IV), which mirrors the evidence-based approach tested in MRCP 1
- These guidelines cover the common dermatological conditions frequently tested in postgraduate examinations, including contact dermatitis, basal cell carcinoma, and squamous cell carcinoma 1
High-Yield Clinical Conditions
Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis (SJS/TEN) - this is a critical emergency topic:
- Master the SCORTEN prognostic scoring system 2
- Know the immediate management steps: discontinue culprit drugs, calculate body surface area involvement using Lund and Browder charts, assess airway patency with anaesthetic involvement 2
- Understand the investigation panel: full blood count, C-reactive protein, urea and electrolytes, liver function tests, coagulation studies, mycoplasma and chlamydia serology, HSV swabs 2
- Recognize admission criteria: >10% BSA epidermal involvement, relevant comorbidities (malignancy, previous stem cell transplant), or need for ventilation 2
Melanoma staging and prognostic factors:
- Breslow thickness, ulceration status, and mitotic rate are the critical pathology parameters 2
- For stage III disease, know that number of metastatic nodes and clinical nodal status (nonpalpable vs. palpable) are most important predictors 2
- For stage IV disease, site of metastasis and elevated LDH are the significant predictors 2
- Sentinel lymph node biopsy status is the most important prognostic factor in localized melanoma 2
Basal Cell Carcinoma (BCC) - understand the clinical variants:
- Recognize morphological presentations: nodular, cystic, superficial, morphoeic (sclerosing), keratotic, and pigmented variants 3
- Identify warning signs of aggressive behavior: poorly defined clinical margins, rapid growth, neurologic symptoms, high-risk locations (central face, eyelids, periorbital skin, nose, lips, ears) 3
- Know that basosquamous carcinoma has higher metastatic potential than typical BCC 3
- Risk factors include fair skin, red/blond hair, light eye color, extensive sun exposure in childhood, immunosuppression, and previous radiation therapy 3
Study Approach
Systematic Learning Method
- Use the BAD guideline structure to organize your knowledge - each guideline follows a consistent format with clear recommendations and evidence levels 2
- Focus on strong recommendations (most people should receive the intervention) versus weak recommendations (consider pros/cons for individual patients) 2
- Pay attention to the GRADE methodology used in BAD guidelines from 2016 onwards, as this reflects modern evidence-based medicine principles tested in MRCP 2
Clinical Examination Skills
- Practice systematic dermatological assessment: record vital signs, assess airway patency, examine respiratory system, examine skin for target lesions, atypical targets, purpuric macules, blisters, and epidermal detachment 2
- For any skin lesion, document: Breslow thickness, ulceration status, mitotic rate, margin status, satellitosis, and Clark level 2
- Master body surface area estimation using standardized charts 2
Common Pitfalls to Avoid
- Don't underestimate BCC - while it rarely metastasizes (<0.1%), it causes substantial local destruction if untreated, and aggressive histologic subtypes recur more frequently 3
- Don't miss SJS/TEN airway compromise - early involvement of paediatric anaesthetist or intensivist is critical, with immediate availability of difficult intubation equipment 2
- Don't forget multidisciplinary team involvement - SJS/TEN requires coordinated care from dermatology, burns, intensive care, ophthalmology, infectious diseases, and other specialties 2
Evidence Quality Recognition
- Understand that BAD guidelines undergo peer review by the Therapy & Guidelines subcommittee and consultation with all relevant stakeholders including patient groups 2
- Guidelines are updated every 5 years or more frequently for fast-moving topics 2
- The consultation process includes BAD members, British Dermatological Nursing Group, and Primary Care Dermatological Society 2