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Derm CasesDermatology / Dermatopathology / Skin cancer MDT

Derm Cases · Dermatology / Dermatopathology / Skin cancer MDT

OSCE — melanocytic pathology: biopsy, naevus vs melanoma criteria, report elements

An 8-minute OSCE on correct melanoma biopsy technique, architectural criteria distinguishing naevus from melanoma, essential AJCC pathology report elements, PRAME as ancillary only, and MPATH-Dx-style action for ambiguous lesions.

8 minosce1 min readVerification in progress

Target exams

NEET-PGINICETUSMLEPLABMRCP
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Study tools

Target exams

NEET-PGINICETUSMLEPLABMRCP
Prompt
An 8-minute OSCE on correct melanoma biopsy technique, architectural criteria distinguishing naevus from melanoma, essential AJCC pathology report elements, PRAME as ancillary only, and MPATH-Dx-style action for ambiguous lesions.

Brief (to candidate)

You are in a pigmented lesion clinic. A 48-year-old has an irregular back lesion. The trainee pathologist asks how you will biopsy it and what you need on the report if melanoma is confirmed. In 8 minutes, set out a safe clinicopathologic plan.

[2]

Candidate instructions

  1. State preferred biopsy technique and why shave understages.
  2. List architecture-first criteria naevus vs melanoma.
  3. Name Breslow measurement landmarks and ulceration importance.
  4. Mention PRAME as ancillary only.
  5. Note MPATH-Dx/expert review for ambiguous or adult Spitzoid lesions.
  6. Link invasive melanoma to WLE ± SLNB pathway (staging principles).
[1]

Examiner checklist (mark each domain / 10)

DomainKey actions expected
BiopsyPrefers full-thickness excisional biopsy with narrow margins; flags incomplete superficial shave risk for Breslow understaging[1][2]
CriteriaNames symmetry/maturation vs asymmetry, pagetoid scatter, deep mitoses, sheet-like growth
Report elementsBreslow from granular layer/ulcer base; ulceration; margins; subtype/adverse features[1][2]
AncillaryPRAME/IHC support diagnosis but do not replace morphology[4]
Grey zoneAmbiguous/adult Spitzoid → complete excision + specialist review; MPATH-Dx class language for action[3][5]
Next stepsInvasive melanoma → WLE margins concept ± SLNB discussion per stage
CommunicationClear plan, photography, follow-up for scar and new lesions

Model key actions

  • Excisional full-thickness biopsy first when melanoma is realistic.[2]
  • Architecture constellation over single-feature diagnosis.
  • AJCC-ready report elements for T category.[1]
  • Do not treat PRAME as standalone proof of melanoma.[4]

Common errors

  • Planning shave-only for obvious melanoma.
  • Observing a transected atypical base because “report said possible naevus.”
  • Equating childhood Spitz naevus risk with adult Spitzoid lesions.
[1]
  • Ordering SLNB before histologic confirmation of invasive melanoma.
References5ShowHide
  1. [1]Gershenwald JE, Scolyer RA. Melanoma Staging: American Joint Committee on Cancer (AJCC) 8th Edition and Beyond. Annals of Surgical Oncology, 2018.PMID 29850954
  2. [2]Scolyer RA, Rawson RV, Gershenwald JE, et al. Melanoma pathology reporting and staging. Modern Pathology, 2020.PMID 31758078
  3. [3]Barnhill RL, Elder DE, Piepkorn MW, et al. Revision of the Melanocytic Pathology Assessment Tool and Hierarchy for Diagnosis Classification Schema for Melanocytic Lesions: A Consensus Statement. JAMA Network Open, 2023.PMID 36630138
  4. [4]Lezcano C, Jungbluth AA, Nehal KS, et al. PRAME Expression in Melanocytic Tumors. American Journal of Surgical Pathology, 2018.PMID 30045064
  5. [5]Yeh I, Busam KJ. Spitz melanocytic tumours — a review. Histopathology, 2022.PMID 34958498
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