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. 2020 Jan 2;33(6):1033–1040. doi: 10.1038/s41379-019-0444-0

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© The Author(s) 2020

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 6 — Based on our results patients with no dysplasia (classic and/or differentiated) and retained CK13 staining have a very low risk of malignant transformation and could be referred for less intensive surveillance, while other patients need to remain under regular surveillance. For our cohort this would mean that 22 out of 84 patients (26%) would be eligible for less intensive follow-up. CK13 keratin 13.