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. 2022 Aug 15;22:204. doi: 10.1186/s12902-022-01113-4

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© The Author(s) 2022

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 2 — Representative immunohistochemical results of TIGIT in poorly differentiated thyroid carcinoma (PDTC). Neoplastic cells were arranged in a solid or trabecular architecture (A) (H&E, low magnification). About half of PDTC cells were positive for TIGIT in this area (upper and right) (B). TIGIT-positive area of PDTC (H&E, high magnification) (C). Cytoplasmic TIGIT reactivity was observed (D)