Evidence map›Paper›PMID 33682013›Full record

ArticleVirchows Archiv : an international journal of pathology2021

Histological interpretation of differentiated vulvar intraepithelial neoplasia (dVIN) remains challenging-observations from a bi-national ring-study.

Shatavisha Dasgupta, Elf de Jonge, Mieke R Van Bockstal, Luthy S M Wong-Alcala, Suzanne Wilhelmus, Lex A C F Makkus, Katrien Schelfout, Koen K Van de Vijver, Sander Smits, Etienne Marbaix and 3 more

Abstract read
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Shatavisha DasguptaDepartment of Pathology, Erasmus MC, University Medical Centre, Postbus 2040, Be-building, 3000CA, Rotterdam, The Netherlands. s.dasgupta@erasmusmc.nl.ORCID http://orcid.org/0000-0003-1804-5015
Elf de Jonge *Department of Pathology, Groene Hart Ziekenhuis, Gouda, The Netherlands.
Mieke R Van Bockstal *Department of Pathology, Cliniques Universitaires Saint-Luc Bruxelles, Brussels, Belgium.ORCID https://orcid.org/0000-0003-4498-928X
Luthy S M Wong-Alcala *Department of Pathology, Pathologisch en Cytologisch laboratorium, Breda, The Netherlands.
Suzanne Wilhelmus *Department of Pathology, Pathan B.V., Laboratory for Pathology, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0002-7794-5315
Lex A C F Makkus *Laboratory for Pathology, PAL Dordrecht, Dordrecht, The Netherlands.
Katrien Schelfout *Department of Pathology, Bravis Ziekenhuis, Bergen op Zoom, The Netherlands.
Koen K Van de Vijver *Department of Pathology, Cancer Research Institute Ghent, Ghent University Hospital, Ghent, Belgium.ORCID https://orcid.org/0000-0002-2026-9790
Sander Smits *Department of Pathology, Pathan B.V., Laboratory for Pathology, Rotterdam, The Netherlands.
Etienne Marbaix *Department of Pathology, Cliniques Universitaires Saint-Luc Bruxelles, Brussels, Belgium.ORCID https://orcid.org/0000-0002-9403-1072
Senada KoljenovićDepartment of Pathology, Erasmus MC, University Medical Centre, Postbus 2040, Be-building, 3000CA, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0002-5185-3455
Folkert J van KemenadeDepartment of Pathology, Erasmus MC, University Medical Centre, Postbus 2040, Be-building, 3000CA, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0002-4225-4354
Patricia C Ewing-GrahamDepartment of Pathology, Erasmus MC, University Medical Centre, Postbus 2040, Be-building, 3000CA, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0002-1779-1115

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Differentiated vulvar intraepithelial neoplasia (dVIN) is a premalignant lesion that is known to progress rapidly to invasive carcinoma. Accurate histological diagnosis is therefore crucial to allow appropriate treatment. To identify reliable diagnostic features, we evaluated the inter-observer agreement in the histological assessment of dVIN, among a bi-national, multi-institutional group of pathologists. Two investigators from Erasmus MC selected 36 hematoxylin-eosin-stained glass slides of dVIN and no-dysplasia, and prepared a list of 15 histological features of dVIN. Nine participating pathologists (i) diagnosed each slide as dVIN or no-dysplasia, (ii) indicated which features they used for the diagnosis, and (iii) rated these features in terms of their diagnostic usefulness. Diagnoses rendered by > 50% participants were taken as the consensus (gold standard). p53-immunohistochemistry (IHC) was performed for all cases, and the expression patterns were correlated with the consensus diagnoses. Kappa (ĸ)-statistics were computed to measure inter-observer agreements, and concordance of the p53-IHC patterns with the consensus diagnoses. For the diagnosis of dVIN, overall agreement was moderate (ĸ = 0.42), and pair-wise agreements ranged from slight (ĸ = 0.10) to substantial (ĸ = 0.73). Based on the levels of agreement and ratings of usefulness, the most helpful diagnostic features were parakeratosis, cobblestone appearance, chromatin abnormality, angulated nuclei, atypia discernable under × 100, and altered cellular alignment. p53-IHC patterns showed substantial concordance (ĸ = 0.67) with the consensus diagnoses. Histological interpretation of dVIN remains challenging with suboptimal inter-observer agreement. We identified the histological features that may facilitate the diagnosis of dVIN. For cases with a histological suspicion of dVIN, consensus-based pathological evaluation may improve the reliability of the diagnosis.

Indexed as

Cell DifferentiationBelgiumBiomarkers, TumorBiopsyCarcinoma in SituCyclin-Dependent Kinase Inhibitor p16FemaleHumansImmunohistochemistryNetherlandsObserver VariationPredictive Value of TestsReproducibility of ResultsTumor Suppressor Protein p53Vulvar NeoplasmsBiomarkers, TumorCDKN2A protein, humanCyclin-Dependent Kinase Inhibitor p16TP53 protein, humanTumor Suppressor Protein p53Carcinoma in situHistologyLower genital tractObserver variationVulvar diseases

Identifiers

PMID33682013
PMCPMC8364542

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.