Computer-Aided Assessment of Melanocytic Lesions by Means of a Mitosis Algorithm
Open accessAbstract
An increasing number of pathology laboratories are now fully digitised, using whole slide imaging (WSI) for routine diagnostics. WSI paves the road to use artificial intelligence (AI) that will play an increasing role in computer-aided diagnosis (CAD). In melanocytic skin lesions, the presence of a dermal mitosis may be an important clue for an intermediate or a malignant lesion and may indicate worse prognosis. In this study a mitosis algorithm primarily developed for breast carcinoma is applied to melanocytic skin lesions. This study aimed to assess whether the algorithm could be used in diagnosing melanocytic lesions, and to study the added value in diagnosing melanocytic lesions in a practical setting. WSI’s of a set of hematoxylin and eosin (H&E) stained slides of 99 melanocytic lesions (35 nevi, 4 intermediate melanocytic lesions, and 60 malignant melanomas, including 10 nevoid melanomas), for which a consensus diagnosis was reached by three academic pathologists, were subjected to a mitosis algorithm based on AI. Two academic and six general pathologists specialized in dermatopathology examined the WSI cases two times, first without mitosis annotations and after a washout period of at least 2 months with mitosis annotations based on the algorithm. The algorithm indicated true mitosis in lesional cells, i.e., melanocytes, and non-lesional cells, i.e., mainly keratinocytes and inflammatory cells. A high number of false positive mitosis was indicated as well, comprising melanin pigment, sebaceous glands nuclei, and spindle cell nuclei such as stromal cells and neuroid differentiated melanocytes. All but one pathologist reported more often a dermal mitosis with the mitosis algorithm, which on a regular basis, was incorrectly attributed to mitoses from mainly inflammatory cells. The overall concordance of the pathologists with the consensus diagnosis for all cases excluding nevoid melanoma (n = 89) appeared to be comparable with and without the use of AI (89% vs. 90%). However, the concordance increased by using AI in nevoid melanoma cases (n = 10) (75% vs. 68%). This study showed that in general cases, pathologists perform similarly with the aid of a mitosis algorithm developed primarily for breast cancer. In nevoid melanoma cases, pathologists perform better with the algorithm. From this study, it can be learned that pathologists need to be aware of potential pitfalls using CAD on H&E slides, e.g., misinterpreting dermal mitoses in non-melanotic cells.
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In Sturm et al.'s study, overall diagnostic concordance with expert consensus was similar (~90%) with and without algorithm annotations.
“While overall diagnostic concordance with expert consensus was similar (~90%)”
From Artificial Intelligence in Dermatopathology: An Update and Review of the Current Literature (2026) · cites this paper as [32]
The Results report similar concordance with and without AI (89% versus 90%), but that comparison excludes the 10 nevoid melanoma cases. The unqualified claim implies the figure covers all cases, whereas the paper reports improved concordance with AI for nevoid melanoma. (LLM, conf=0.85)
Experimental — accuracy not yet measuredThe AI mitosis detection tool flagged numerous false positives (e.g., pigmented or keratinocyte nuclei).
“The AI flagged numerous false positives (e.g., pigmented or keratinocyte nuclei), underscoring the need for cautious interpretation.”
From Artificial Intelligence in Dermatopathology: An Update and Review of the Current Literature (2026) · cites this paper as [32]
The Materials and Methods (§2.2) and Discussion (§4) report numerous false-positive detections, including melanin pigment and several kinds of nuclei. But the Results (§3) describe detections in keratinocytes as non-lesional mitoses, not keratinocyte nuclei falsely identified as mitoses. The paper also cautions against misinterpreting such detections. (LLM, conf=0.87)
Experimental — accuracy not yet measuredIn nevoid melanoma cases, the AI mitosis detection algorithm improved diagnostic concordance from 68% to 75%.
“in nevoid melanoma cases, the algorithm improved concordance from 68% to 75%.”
From Artificial Intelligence in Dermatopathology: An Update and Review of the Current Literature (2026) · cites this paper as [32]
Mitosis detection algorithms may be helpful in particularly challenging cases like nevoid melanoma but offer limited benefit in routine lesion interpretation.
“These findings suggest that mitosis detection algorithms may be helpful in particularly challenging cases like nevoid melanoma but offer limited benefit in routine lesion interpretation.”
From Artificial Intelligence in Dermatopathology: An Update and Review of the Current Literature (2026) · cites this paper as [32]
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Cites
Ehteshami Bejnordi, B., Veta, M., Johannes van Diest, P., van Ginneken, B., Karssemeijer, N., Litjens, G., van der Laak, J. A. W. M., and the CAMELYON16 Consortium, Hermsen, M., Manson, Q. F., et al. (2017) · JAMA · doi:10.1001/jama.2017.14585 · Cited by 3,293 · see citing works
Deep learning as a tool for increased accuracy and efficiency of histopathological diagnosis
Litjens, G., Sánchez, C. I., Timofeeva, N., Hermsen, M., Nagtegaal, I., Kovacs, I., Hulsbergen - van de Kaa, C., Bult, P., van Ginneken, B., & van der Laak, J. (2016) · Scientific Reports · doi:10.1038/srep26286 · Cited by 1,069 · see citing works
Classification of breast cancer histology images using Convolutional Neural Networks
Araújo, T., Aresta, G., Castro, E., Rouco, J., Aguiar, P., Eloy, C., Polónia, A., & Campilho, A. (2017) · PLoS ONE · doi:10.1371/journal.pone.0177544 · Cited by 1,017 · see citing works
Increasing Burden of Melanoma in the United States
Linos, E., Swetter, S. M., Cockburn, M., Colditz, G. A., & Clarke, C. A. (2009) · Journal of Investigative Dermatology · doi:10.1038/jid.2008.423 · Cited by 747 · see citing works
Bulten, W., Pinckaers, H., van Boven, H., Vink, R., de Bel, T., van Ginneken, B., van der Laak, J., Hulsbergen-van de Kaa, C., & Litjens, G. (2020) · The Lancet Oncology · doi:10.1016/s1470-2045(19)30739-9 · Cited by 705 · see citing works
Cruz-Roa, Á., Gilmore, H. L., Basavanhally, A. N., Feldman, M. D., Ganesan, S., Shih, N. N. C., Tomaszewski, J., Gonzalez, F. A., & Madabhushi, A. (2017) · Scientific Reports · doi:10.1038/srep46450 · Cited by 530 · see citing works
Steiner, D. F., MacDonald, R., Liu, Y., Truszkowski, P., Hipp, J. D., Gammage, C., Thng, F., Peng, L., & Stumpe, M. C. (2018) · American Journal of Surgical Pathology · doi:10.1097/pas.0000000000001151 · Cited by 489 · see citing works
Assessment of algorithms for mitosis detection in breast cancer histopathology images
Veta, M., van Diest, P. J., Willems, S. M., Wang, H., Madabhushi, A., Cruz-Roa, Á., Gonzalez, F. A., Larsen, A., Vestergaard, J. S., Dahl, A. B., et al. (2014) · Medical Image Analysis · doi:10.1016/j.media.2014.11.010 · Cited by 480 · see citing works
PRAME Expression in Melanocytic Tumors
Lezcano, C. M., Jungbluth, A. A., Nehal, K. S., Hollmann, T. J., & BUSAM, K. J. (2018) · The American Journal of Surgical Pathology · doi:10.1097/pas.0000000000001134 · Cited by 429 · see citing works
Whole slide imaging in pathology: advantages, limitations, and emerging perspectives
Pantanowitz, L., Farahani, N., & Parwani, A. V. (2015) · Pathology and Laboratory Medicine International · doi:10.2147/plmi.s59826 · Cited by 387 · see citing works
Multifeature Prostate Cancer Diagnosis and Gleason Grading of Histological Images
Tabesh, A., Teverovskiy, M., Pang, H.-Y., Kumar, V. P., Verbel, D., Kotsianti, A., & Saidi, O. (2007) · IEEE Transactions on Medical Imaging · doi:10.1109/tmi.2007.898536 · Cited by 351 · see citing works
A new understanding in the epidemiology of melanoma
Erdei, E., & Torres, S. M. (2010) · Expert Review of Anticancer Therapy · doi:10.1586/era.10.170 · Cited by 344 · see citing works
Predicting breast tumor proliferation from whole-slide images: The TUPAC16 challenge
Veta, M., Heng, Y. J., Stathonikos, N., Bejnordi, B. E., de Beça, F. F., Wollmann, T., Rohr, K., Shah, M., Wang, D., Rousson, M., et al. (2019) · Medical Image Analysis · doi:10.1016/j.media.2019.02.012 · Cited by 309 · see citing works
Mitosis detection in breast cancer histological images An ICPR 2012 contest
Roux, L., Racoceanu, D., Loménie, N., Kulikova, M. S., Irshad, H., Jacques, K., Capron, F., Genestie, C., Naour, G. L., & Gurcan Metin, N. (2013) · Journal of Pathology Informatics · doi:10.4103/2153-3539.112693 · Cited by 303 · see citing works
Tellez, D., Balkenhol, M., Otte-Höller, I., van de Loo, R., Vogels, R., Bult, P., Wauters, C., Vreuls, W., Mol, S., Karssemeijer, N., et al. (2018) · IEEE Transactions on Medical Imaging · doi:10.1109/tmi.2018.2820199 · Cited by 288 · see citing works
Self-citationPathologist-level classification of histopathological melanoma images with deep neural networks
Hekler, A., Utikal, J. S., Enk, A. H., Berking, C., Klode, J., Schadendorf, D., Jansen, P., Franklin, C., Holland-Letz, T., Krahl, D., et al. (2019) · European Journal of Cancer · doi:10.1016/j.ejca.2019.04.021 · Cited by 231 · see citing works
Efficient deep learning model for mitosis detection using breast histopathology images
Saha, M., Chakraborty, C., & Racoceanu, D. (2017) · Computerized Medical Imaging and Graphics · doi:10.1016/j.compmedimag.2017.12.001 · Cited by 196 · see citing works
Francken, A. B., Shaw, H. M., Thompson, J. F., Soong, S., Accortt, N. A., Azzola, M. F., Scolyer, R. A., Milton, G. W., McCarthy, W. H., Colman, M. H., et al. (2004) · Annals of Surgical Oncology · doi:10.1245/aso.2004.07.014 · Cited by 193 · see citing works
Bejnordi, B. E., Zuidhof, G., Balkenhol, M. C. A., Hermsen, M., Bult, P., van Ginneken, B., Karssemeijer, N., Litjens, G. J. S., & van der Laak, J. A. W. M. (2017) · Journal of medical imaging · doi:10.1117/1.jmi.4.4.044504 · Cited by 186 · see citing works
Nagore, E., Oliver, V., Estrada, R. B., Moreno-Picot, S., Insa, A., & Fortea, J. M. (2005) · Melanoma Research · doi:10.1097/00008390-200506000-00005 · Cited by 143 · see citing works
Gavrielides, M. A., Gallas, B. D., Lenz, P., Badano, A. G., & Hewitt, S. M. (2011) · Archives of Pathology & Laboratory Medicine · doi:10.5858/135.2.233 · Cited by 132 · see citing works
Evaluating the benefits of digital pathology implementation: time savings in laboratory logistics
Baidoshvili, A., Bucur, A., van Leeuwen, J., van der Laak, J. A. W. M., Kluin, P. M., & van Diest, P. J. (2018) · Histopathology · doi:10.1111/his.13691 · Cited by 129 · see citing works
Veta, M., van Diest, P. J., Jiwa, M., Al-Janabi, S., & Pluim, J. P. W. (2016) · PLOS ONE · doi:10.1371/journal.pone.0161286 · Cited by 127 · see citing works
Comparison of pHH3, Ki-67, and Survivin Immunoreactivity in Benign and Malignant Melanocytic Lesions
Nasr, M. R., & El-Zammar, O. A. (2008) · American Journal of Dermatopathology · doi:10.1097/dad.0b013e3181624054 · Cited by 121 · see citing works
Olsen, T. G., Jackson, B. H., Feeser, T. A., Kent, M. N., Moad, J. C., Krishnamurthy, S., Lunsford, D. D., & Soans, R. E. (2018) · Journal of Pathology Informatics · doi:10.4103/jpi.jpi_31_18 · Cited by 119 · see citing works
Deep learning assisted mitotic counting for breast cancer
Balkenhol, M. C. A., Tellez, D., Vreuls, W., Clahsen, P. C., Pinckaers, H., Ciompi, F., Bult, P., & van der Laak, J. A. W. M. (2019) · Laboratory Investigation · doi:10.1038/s41374-019-0275-0 · Cited by 119 · see citing works
The importance of mitotic rate as a prognostic factor for localized cutaneous melanoma
Barnhill, R. L., Katzen, J., Spatz, A., Fine, J., & Berwick, M. (2005) · Journal of Cutaneous Pathology · doi:10.1111/j.0303-6987.2005.00310.x · Cited by 117 · see citing works
Uguen, A., Talagas, M., Costa, S., Duigou, S., Bouvier, S., Braekeleer, M. D., & Marcorelles, P. (2015) · Diagnostic Pathology · doi:10.1186/s13000-015-0431-9 · Cited by 96 · see citing works
Nielsen, P. S., Riber‐Hansen, R., Jensen, T. Ø., Schmidt, H., & Steiniche, T. (2012) · Modern Pathology · doi:10.1038/modpathol.2012.188 · Cited by 94 · see citing works
The Burden of Skin and Subcutaneous Diseases in the United States From 1990 to 2017
Laughter, M. R., Maymone, M. B. C., Karimkhani, C., Rundle, C. W., Hu, S., Wolfe, S. M., Abuabara, K., Hollingsworth, P., Weintraub, G. S., Dunnick, C. A., et al. (2020) · JAMA Dermatology · doi:10.1001/jamadermatol.2020.1573 · Cited by 71 · see citing works
The utility of PRAME staining in identifying malignant transformation of melanocytic nevi
Lohman, M. E., Steen, A. J., Grekin, R. C., & North, J. P. (2021) · Journal of Cutaneous Pathology · doi:10.1111/cup.13958 · Cited by 63 · see citing works
de la Fouchardière, A., Blokx, W. A. M., van Kempen, L. C. L. T., Luzar, B., Piperno-Neumann, S., Puig, S., Alós, L., Calonje, E. J., Massi, D., on behalf of the ESP Dermatopathology Working Group, et al. (2021) · Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin · doi:10.1007/s00428-020-03005-1 · Cited by 55 · see citing works
Self-citationGassenmaier, M., Hahn, M., Metzler, G., Bauer, J. M., Yazdi, A. S., Keim, U., Garbe, C., Wagner, N. B., & Forchhammer, S. (2021) · Cancers · doi:10.3390/cancers13153864 · Cited by 51 · see citing works
Predictors of sentinel lymph node positivity in thin melanoma using the National Cancer Database
Conic, R. R. Z., Ko, J. S., Damiani, G. B., Funchain, P., Knackstedt, T., Vij, A., Vidimos, A. T., & Gastman, B. (2018) · Journal of the American Academy of Dermatology · doi:10.1016/j.jaad.2018.08.051 · Cited by 50 · see citing works
Han, W., Johnson, C., Gaed, M., Gómez, J. A., Moussa, M., Chin, J. L., Pautler, S. E., Bauman, G. S., & Ward, A. D. (2020) · Scientific Reports · doi:10.1038/s41598-020-66849-2 · Cited by 37 · see citing works
Validation of mitotic cell quantification via microscopy and multiple whole-slide scanners
Tabata, K., Uraoka, N., Benhamida, J. K., Hanna, M. G., Sirintrapun, S. J., Gallas, B. D., Gong, Q., Aly, R. G. M., Emoto, K., Matsuda, K. M., et al. (2019) · Diagnostic Pathology · doi:10.1186/s13000-019-0839-8 · Cited by 35 · see citing works
Machine learning techniques for mitoses classification
Nofallah, S., Mehta, S., Mercan, E., Knezevich, S. R., May, C. J., Weaver, D. L., Witten, D., Elmore, J. G., & Shapiro, L. G. (2020) · Computerized Medical Imaging and Graphics · doi:10.1016/j.compmedimag.2020.101832 · Cited by 31 · see citing works
Reproducibility in the automated quantitative assessment of HER2/neu for breast cancer
Keay, T. C., Conway, C. M., O’Flaherty, N., Hewitt, S. M., Shea, K. I., & Gavrielides, M. A. (2013) · Journal of Pathology Informatics · doi:10.4103/2153-3539.115879 · Cited by 27 · see citing works
The evolution of machine learning: past, present, and future
Cohen, S. (2020) · Elsevier eBooks · doi:10.1016/b978-0-323-67538-3.00001-4 · Cited by 25 · see citing works
Melanoma Diagnosis: The Importance of Histopathological Report
Filosa, A., & Filosa, G. (2018) · Dermatopathology · doi:10.1159/000486670 · Cited by 22 · see citing works
Andres, C., Andres-Belloni, B., Hein, R., Biedermann, T., Schäpe, A., Brieu, N., Schönmeyer, R., Yiğitsoy, M., Ring, J., Schmidt, G., et al. (2017) · Journal of the European Academy of Dermatology and Venereology · doi:10.1111/jdv.14126 · Cited by 16 · see citing works
Automated quantification of Ki67/ MART1 stains may prevent false‐negative melanoma diagnoses
Wandler, A., Spaun, E., Steiniche, T., & Nielsen, P. S. (2016) · Journal of Cutaneous Pathology · doi:10.1111/cup.12778 · Cited by 11 · see citing works
Sturm, B., Creytens, D., Cook, M. G., Smits, J., van Dijk, M. C. R. F., Eijken, E., Kurpershoek, E., Küsters‐Vandevelde, H. V. N., Ooms, A. H. A. G., Wauters, C. A. P., et al. (2019) · Journal of Pathology Informatics · doi:10.4103/jpi.jpi_46_18 · Cited by 10 · see citing works
Self-citation
Flagged first, then by citations
Research works printed but not linked: 2
- [2]Tomaszewski J. Overview of the role of artificial intelligence in pathology: The computer as a pathology digital assistent Artificial Intelligence and Deep Learning in Pathology 1st ed. Cohen S. Elsevier Amsterdam, The Netherland 2021
- [7]Howlader N. Noone A.M. Krapcho M. Miller D. Brest A. Yu M. Ruhl J. Tatalovich Z. Mariotto A. Lewis D.R. SEER Cancer Statistics Review, 1975–2018 National Cancer Institute Bethesda, MD, USA 2021
Cited by
Sorted by citations
Deep Learning for Skin Melanocytic Tumors in Whole-Slide Images: A Systematic Review
Mosquera‐Zamudio, A., Launet, L., Tabatabaei, Z., Parra-Medina, R. S., Colomer, A., Moll, J. O., Monteagudo, C. C., Janssen, E. A. M., & Naranjo, V. (2022) · Cancers · doi:10.3390/cancers15010042 · Cited by 33 · see citing works
Recent Advances in Melanoma Diagnosis and Prognosis Using Machine Learning Methods
Grossarth, S. N., Mosley, D. A., Madden, C., Ike, J., Smith, I. T., Huo, Y., & Wheless, L. (2023) · Current Oncology Reports · doi:10.1007/s11912-023-01407-3 · Cited by 33 · see citing works
Artificial Intelligence in Digital Pathology for Bladder Cancer: Hype or Hope? A Systematic Review
Khoraminia, F., Fuster, S., Kanwal, N., Olislagers, M., Engan, K., van Leenders, G. J. L. H., Stubbs, A., Akram, F., & Zuiverloon, T. C. M. (2023) · Cancers · doi:10.3390/cancers15184518 · Cited by 28 · see citing works
Grant, S. R., Andrew, T. W., Alvarez, E. V., Huss, W. J., & Paragh, G. (2022) · Cancers · doi:10.3390/cancers14246231 · Cited by 25 · see citing works
Mini review on skin biopsy: traditional and modern techniques
Alwahaibi, N., & Alwahaibi, M. (2025) · Frontiers in Medicine · doi:10.3389/fmed.2025.1476685 · Cited by 12 · see citing works
Cocuz, I. G., Niculescu, R., Popelea, M. C., Cocuz, M. E., Sabău, A.-H., Tinca, A. C., Cozac-Szőke, A. R., Chiorean, D. M., Budin, C. E., & Cotoi, O. S. (2025) · Diagnostics · doi:10.3390/diagnostics15172196 · Cited by 7 · see citing works
Basic elements of artificial intelligence tools in the diagnosis of cutaneous melanoma
Querzoli, G., Veronesi, G., Corti, B., Nottegar, A., & Dika, E. (2023) · Critical Reviews™ in Oncogenesis · doi:10.1615/critrevoncog.2023050220 · Cited by 6 · see citing works
Machine learning to detect melanoma exploiting nuclei morphology and Spatial organization
Veronesi, G., Curti, N., Gardini, A., Querzoli, G., Castellani, G., & Dika, E. (2025) · Scientific Reports · doi:10.1038/s41598-025-02913-z · Cited by 6 · see citing works
Artificial Intelligence in Melanoma Dermatopathology: A Review of Literature
Neimy, H., Helmy, J., Snyder, A., & Valdebran, M. (2023) · American Journal of Dermatopathology · doi:10.1097/dad.0000000000002593 · Cited by 5 · see citing works
Wu, C., Chang, M.-H., Chen, H., Tsai, H.-H., Chien, C.-J., & Wang, J.-C. (2025) · Clinical Breast Cancer · doi:10.1016/j.clbc.2025.04.021 · Cited by 4 · see citing works
A Review of Artificial Intelligence in Dermatopathology
Prestwood, C. A., Gibbs, D. C., Wolner, Z. J., & Stoff, B. K. (2025) · Dermatologic Clinics · doi:10.1016/j.det.2025.05.006 · Cited by 3 · see citing works
Artificial Intelligence in Dermatopathology: An Update and Review of the Current Literature
Abu-Dayeh, A., Cazzato, G., & Giubellino, A. (2026) · Diagnostics · doi:10.3390/diagnostics16111702 · Cited by 1 · see citing works
“Sturm et al. evaluated an AI-based mitosis detection tool, which was originally designed for breast cancer, on 99 digitized melanocytic lesion slides (including 10 nevoid melanomas) [32].”
Large-Scale Dermatopathology Dataset for Lesion Segmentation: Model Development and Analysis
Chong, Y., Park, D., Ahn, Y., Kwak, Y., Park, S., Back, S. W., Lee, C.-W., Park, G., Alam, M. R., Kim, B. K., et al. (2025) · Journal of Korean Medical Science · doi:10.3346/jkms.2025.40.e220 · Cited by 1 · see citing works
- Authors
- Sturm, B., Creytens, D., Smits, J., Ooms, A. H. A. G., Eijken, E., Kurpershoek, E., Küsters-Vandevelde, H. V. N., Wauters, C., Blokx, W. A. M., & van der Laak, J. A. W. M.
- Affiliations
- Radboud University Medical Center (NL)
- Ghent University Hospital (BE)
- Pathan B.V., 3045 PM Rotterdam, The Netherlands
- Laboratory for Pathology Oost Nederland (LabPON), 7550 AM Hengelo, The Netherlands
- Department of Pathology, Canisius Wilhelmina Hospital, 6500 GS Nijmegen, The Netherlands
- Canisius-Wilhelmina Ziekenhuis (NL)
- University Medical Center Utrecht (NL)
- Department of Pathology, Radboud University Medical Center, 6500 HB Nijmegen, The Netherlands
- Venue
- Diagnostics
- Publisher
- MDPI AG
- Published
- 2022-02-08
- Volume
- 12
- Issue
- 2
- Pages
- 436
- ISSN
- 2075-4418 (ISSN-L)
- PMC
- PMC8871065
- OpenAlex
- W4211247273
- Cited by
- 13
- References
- 43
- Citations by year
- 2026: 1 · 2025: 6 · 2023: 4 · 2022: 2
- FWCI
- 0.99
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Diagnostics (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Ghent University Academic Bibliography (Ghent University) (submittedVersion, cc-by)
- KTH Publication Database DiVA (KTH Royal Institute of Technology) (submittedVersion, other-oa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Utrecht University Repository (Utrecht University) (submittedVersion, other-oa)
- Radboud Repository (Radboud University) (submittedVersion)
- Radboud Repository (Radboud University) (submittedVersion, other-oa)
- Funders
- European Federation of Pharmaceutical Industries and Associations
- European Commission (945358)
- Knut och Alice Wallenbergs Stiftelse
- Topics
- Physical Sciences › Computer Science › Artificial Intelligence › AI in cancer detection
- Health Sciences › Medicine › Oncology › Cutaneous Melanoma Detection and Management
- Health Sciences › Medicine › Health Informatics › Artificial Intelligence in Healthcare and Education
- Keywords
- melanocytic lesions, computer-aided diagnosis, whole slide imaging, nevoid melanoma, melanoma, melanocytic nevi, dermatopathology, algorithm transferability, H&E staining
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