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. 2022 Sep 28;22:1021. doi: 10.1186/s12885-022-10114-4

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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. 4 — Periphery of SGC tumors. Thirteen patients with mucoepidermoid carcinoma (MEC), ten patients with adenoid cystic carcinoma (AdCC), eight patients with acinic cell carcinoma (ACC), six patients with salivary duct carcinoma (SDC) and six patients with adenocarcinoma not otherwise specified (AdCaNOS) were included. A significant difference in CD47 expression between tumor cells and TIICs was observed in the periphery of MEC tumors