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Derm CasesDermatology / Dermatopathology

Derm Cases · Dermatology / Dermatopathology

OSCE — inflammatory dermatopathology: patterns, sampling, DIF, PAS

An 8-minute OSCE on Ackerman-style pattern diagnosis, correct biopsy choice for inflammatory disease, PAS for spongiotic plaques, DIF sampling for blisters, and recognising LCV versus non-specific perivascular inflammation.

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 Ackerman-style pattern diagnosis, correct biopsy choice for inflammatory disease, PAS for spongiotic plaques, DIF sampling for blisters, and recognising LCV versus non-specific perivascular inflammation.

Brief (to candidate)

You are teaching a resident how to request and interpret inflammatory skin biopsies. Three scenarios: scaly foot plaque; tense blisters in an elderly man; palpable purpura. In 8 minutes, give a pattern-based sampling and interpretation plan.

[1]

Candidate instructions

  1. State pattern-first method (Ackerman-style).
  2. Choose biopsy type/depth for each scenario.
  3. Mention PAS for spongiotic foot disease.
  4. Plan H&E + perilesional DIF for blisters; contrast PV vs BP DIF patterns.
  5. Define true LCV histologically.
  6. Name at least two pitfalls (treated centre, no fat for panniculitis, overcalling MF).
[1]

Examiner checklist (mark each domain / 10)

DomainKey actions expected
Pattern methodStarts with dominant reaction pattern then clinical correlation[1][2]
SamplingPunch to adequate depth; deep sample if panniculitis; not shave for deep disease[3]
Spongiotic trapPAS to exclude dermatophyte on foot/hand “eczema”[2]
Blister/DIFPerilesional DIF; intercellular IgG net (PV) vs linear BMZ IgG/C3 (BP)[4]
VasculitisFibrinoid necrosis + neutrophilic debris, not mere perivascular lymphs
Interface/LP awarenessCan name lichenoid band as LP prototype pattern[5]
SafetyInterface necrosis + sick/mucosal patient → SCAR pathway thinking

Model key actions

  • Pattern → special studies → clinicopathologic synthesis.[1]
  • Correct DIF site and blister algorithm.[4]
  • Do not call every rash “non-specific dermatitis” without PAS/drug history when relevant.

Common errors

  • Shave of suspected panniculitis.
  • DIF from necrotic blister base only.
  • Missing tinea on spongiotic biopsies.
  • Labelling mild perivascular lymphocytes as vasculitis.
[1]
References5ShowHide
  1. [1]Ackerman AB. An algorithmic method for histologic diagnosis of inflammatory and neoplastic skin diseases by analysis of their patterns. American Journal of Dermatopathology, 1985.PMID 4025726
  2. [2]Smith EH, Chan MP. Inflammatory Dermatopathology for General Surgical Pathologists. Clinics in Laboratory Medicine, 2017.PMID 28802506
  3. [3]Greenwood JD, Merry SP, Boswell CL. Skin Biopsy Techniques. Primary Care, 2022.PMID 35125151
  4. [4]Schmidt E, Kasperkiewicz M, Joly P. Pemphigus. The Lancet, 2019.PMID 31498102
  5. [5]Ioannides D, Vakirlis E, Kemeny L, et al. European S1 guidelines on the management of lichen planus. Journal of the European Academy of Dermatology and Venereology, 2020.PMID 32678513
PreviousOSCE — dense dermal infiltrate: separate pseudolymphoma, CTCL, and LCH pathwaysDermatology / DermatopathologyNextOSCE — order the right stains and DIF without wrecking the sampleDermatology / Dermatopathology