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. 2022 Jun 13;20:199. doi: 10.1186/s12957-022-02671-6

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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. 7 — The histopathological findings and immunostaining. The tumor cells were composed of pleomorphic spindle cells and giant cells, and many typical and atypical mitotic figures were observed (a). On immunostaining, the tumor cells were focally positive for cluster of differentiation (CD) 117/KIT (b), α-smooth muscle actin (c), AE1/AE3 (d), and EMA (e) and negative for CD34 (f), DOG1 (g), h-caldesmon (h), desmin (i), S100 protein (j), and CD45 (k). Ki-67/MIB1 proliferation index was very high (l). (a ×100 magnification, b–l ×200 magnification)