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. 2023 Jul 13;23:67. doi: 10.1186/s40644-023-00589-0

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© The Author(s) 2023

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 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 — Coronal non-fat-suppressed high-spatial-resolution T2-weighted imaging (a, c and e); coronal fat-suppressed isotropic contrast-enhanced three-dimensional high-spatial-resolution T1-weighted imaging (b, d and f). The lymph nodes were signed by white boxes. a-b, Benign node with 3.7 mm in short-axis diameter, showed oval, smooth border, homogeneous signal and homogeneous enhancement. c-d, Benign node with 5.6 mm in short-axis diameter, showed round, irregular border, heterogeneous signal and heterogeneous enhancement. e-f, Malignant node with 5.8 mm in short-axis diameter, showed round, irregular border, heterogeneous signal and heterogeneous enhancement