Same same but different: A Web-based deep learning application revealed classifying features for the histopathologic distinction of cortical malformations.


Journal

Epilepsia
ISSN: 1528-1167
Titre abrégé: Epilepsia
Pays: United States
ID NLM: 2983306R

Informations de publication

Date de publication:
03 2020
Historique:
received: 12 11 2019
revised: 23 01 2020
accepted: 23 01 2020
pubmed: 23 2 2020
medline: 21 10 2020
entrez: 22 2 2020
Statut: ppublish

Résumé

The microscopic review of hematoxylin-eosin-stained images of focal cortical dysplasia type IIb and cortical tuber of tuberous sclerosis complex remains challenging. Both entities are distinct subtypes of human malformations of cortical development that share histopathological features consisting of neuronal dyslamination with dysmorphic neurons and balloon cells. We trained a convolutional neural network (CNN) to classify both entities and visualize the results. Additionally, we propose a new Web-based deep learning application as proof of concept of how deep learning could enter the pathologic routine. A digital processing pipeline was developed for a series of 56 cases of focal cortical dysplasia type IIb and cortical tuber of tuberous sclerosis complex to obtain 4000 regions of interest and 200 000 subsamples with different zoom and rotation angles to train a neural network. Guided gradient-weighted class activation maps (Guided Grad-CAMs) were generated to visualize morphological features used by the CNN to distinguish both entities. Our best-performing network achieved 91% accuracy and 0.88 area under the receiver operating characteristic curve at the tile level for an unseen test set. Novel histopathologic patterns were found through the visualized Guided Grad-CAMs. These patterns were assembled into a classification score to augment decision-making in routine histopathology workup. This score was successfully validated by 11 expert neuropathologists and 12 nonexperts, boosting nonexperts to expert level performance. Our newly developed Web application combines the visualization of whole slide images with the possibility of deep learning-aided classification between focal cortical dysplasia IIb and tuberous sclerosis complex. This approach will help to introduce deep learning applications and visualization for the histopathologic diagnosis of rare and difficult-to-classify brain lesions.

Identifiants

pubmed: 32080846
doi: 10.1111/epi.16447
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

421-432

Informations de copyright

© 2020 The Authors. Epilepsia published by Wiley Periodicals, Inc. on behalf of International League Against Epilepsy.

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Auteurs

Joshua Kubach (J)

Institute of Neuropathology, University Hospitals, Erlangen, Germany.

Angelika Muhlebner-Fahrngruber (A)

Department of (Neuro)Pathology, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, the Netherlands.

Figen Soylemezoglu (F)

Department of Pathology, Faculty of Medicine, Hacettepe University, Ankara, Turkey.

Hajime Miyata (H)

Department of Neuropathology, Research Institute for Brain and Blood Vessels, Akita Cerebrospinal and Cardiovascular Center, Akita, Japan.

Pitt Niehusmann (P)

Department of Neurology/Pathology, Oslo University Hospital, Oslo, Norway.

Mrinalini Honavar (M)

Department of Anatomic Pathology, Pedro Hispano Hospital, Matosinhos, Portugal.

Fabio Rogerio (F)

Department of Pathology, State University of Campinas, Campinas, Brazil.

Se-Hoon Kim (SH)

Department of Pathology, Yonsei University College of Medicine, Seoul, Korea.

Eleonora Aronica (E)

Department of (Neuro)Pathology, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, the Netherlands.
Stichting Epilepsie Instellingen Nederland, Zwolle, the Netherlands.

Rita Garbelli (R)

Epilepsy Unit, Milan, Italy.

Samuel Vilz (S)

Institute of Neuropathology, University Hospitals, Erlangen, Germany.

Alexander Popp (A)

Institute of Neuropathology, University Hospitals, Erlangen, Germany.

Stefan Walcher (S)

Institute of Neuropathology, University Hospitals, Erlangen, Germany.

Christoph Neuner (C)

Institute of Neuropathology, University Hospitals, Erlangen, Germany.

Michael Scholz (M)

Institute of Anatomy, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.

Stefanie Kuerten (S)

Institute of Anatomy, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.

Verena Schropp (V)

Institute of Anatomy, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.

Sebastian Roeder (S)

Department of Neurology, University Hospitals Erlangen, Erlangen, Germany.

Philip Eichhorn (P)

Institute of Pathology, University Hospitals Erlangen, Erlangen, Germany.

Markus Eckstein (M)

Institute of Pathology, University Hospitals Erlangen, Erlangen, Germany.

Axel Brehmer (A)

Institute of Anatomy, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany.

Katja Kobow (K)

Institute of Neuropathology, University Hospitals, Erlangen, Germany.

Roland Coras (R)

Institute of Neuropathology, University Hospitals, Erlangen, Germany.

Ingmar Blumcke (I)

Institute of Neuropathology, University Hospitals, Erlangen, Germany.

Samir Jabari (S)

Institute of Neuropathology, University Hospitals, Erlangen, Germany.

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