Validation of Whole-slide Digitally Imaged Melanocytic Lesions: Does Z-Stack Scanning Improve Diagnostic Accuracy?

Melanoma validation whole-slide image whole-slide imaging z-stack

Journal

Journal of pathology informatics
ISSN: 2229-5089
Titre abrégé: J Pathol Inform
Pays: United States
ID NLM: 101528849

Informations de publication

Date de publication:
2019
Historique:
received: 11 07 2018
accepted: 17 12 2018
entrez: 12 4 2019
pubmed: 12 4 2019
medline: 12 4 2019
Statut: epublish

Résumé

Accurate diagnosis of melanocytic lesions is challenging, even for expert pathologists. Nowadays, whole-slide imaging (WSI) is used for routine clinical pathology diagnosis in several laboratories. One of the limitations of WSI, as it is most often used, is the lack of a multiplanar focusing option. In this study, we aim to establish the diagnostic accuracy of WSI for melanocytic lesions and investigate the potential accuracy increase of z-stack scanning. Z-stack enables pathologists to use a software focus adjustment, comparable to the fine-focus knob of a conventional light microscope. Melanocytic lesions ( An expert consensus diagnosis was achieved in 99 (97%) of cases. Concordance rates between surgical pathologists and the ground truth varied between 75% and 90%, excluding nevoid melanoma cases. Concordance rates of nevoid melanoma varied between 10% and 80%. Pathologists used the software focusing option in 7%-28% of cases, which in 1 case of nevoid melanoma resulted in correcting a misdiagnosis after finding a dermal mitosis. Diagnostic accuracy of melanocytic lesions based on glass slides and WSI is comparable with previous publications. A large variability in diagnostic accuracy of nevoid melanoma does exist. Our results show that z-stack scanning, in general, does not increase the diagnostic accuracy of melanocytic.

Sections du résumé

BACKGROUND BACKGROUND
Accurate diagnosis of melanocytic lesions is challenging, even for expert pathologists. Nowadays, whole-slide imaging (WSI) is used for routine clinical pathology diagnosis in several laboratories. One of the limitations of WSI, as it is most often used, is the lack of a multiplanar focusing option. In this study, we aim to establish the diagnostic accuracy of WSI for melanocytic lesions and investigate the potential accuracy increase of z-stack scanning. Z-stack enables pathologists to use a software focus adjustment, comparable to the fine-focus knob of a conventional light microscope.
MATERIALS AND METHODS METHODS
Melanocytic lesions (
RESULTS RESULTS
An expert consensus diagnosis was achieved in 99 (97%) of cases. Concordance rates between surgical pathologists and the ground truth varied between 75% and 90%, excluding nevoid melanoma cases. Concordance rates of nevoid melanoma varied between 10% and 80%. Pathologists used the software focusing option in 7%-28% of cases, which in 1 case of nevoid melanoma resulted in correcting a misdiagnosis after finding a dermal mitosis.
CONCLUSION CONCLUSIONS
Diagnostic accuracy of melanocytic lesions based on glass slides and WSI is comparable with previous publications. A large variability in diagnostic accuracy of nevoid melanoma does exist. Our results show that z-stack scanning, in general, does not increase the diagnostic accuracy of melanocytic.

Identifiants

pubmed: 30972225
doi: 10.4103/jpi.jpi_46_18
pii: S2153-3539(22)00369-8
pmc: PMC6415522
doi:

Types de publication

Journal Article

Langues

eng

Pagination

6

Déclaration de conflit d'intérêts

There are no conflicts of interest.

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Auteurs

Bart Sturm (B)

Department of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.

David Creytens (D)

Department of Pathology, Ghent University Hospital, Ghent, Belgium.

Martin G Cook (MG)

Department of Histopathology, Royal Surrey County Hospital, Guildford, United Kingdom.

Jan Smits (J)

Pathan B.V., Rotterdam, The Netherlands.

Marcory C R F van Dijk (MCRF)

Pathology-DNA, Rijnstate Hospital, Arnhem, The Netherlands.

Erik Eijken (E)

Laboratory for Pathology East Netherlands (LabPON), Hengelo, The Netherlands.

Eline Kurpershoek (E)

Pathan B.V., Rotterdam, The Netherlands.

Heidi V N Küsters-Vandevelde (HVN)

Department of Pathology, Canisius Wilhelmina Hospital, Nijmegen, The Netherlands.

Ariadne H A G Ooms (AHAG)

Pathan B.V., Rotterdam, The Netherlands.

Carla Wauters (C)

Department of Pathology, Canisius Wilhelmina Hospital, Nijmegen, The Netherlands.

Willeke A M Blokx (WAM)

Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.

Jeroen A W M van der Laak (JAWM)

Department of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.

Classifications MeSH