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©The Author(s) 2024. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Clin Cases. Sep 6, 2024; 12(25): 5798-5804
Published online Sep 6, 2024. doi: 10.12998/wjcc.v12.i25.5798
Published online Sep 6, 2024. doi: 10.12998/wjcc.v12.i25.5798
Rare giant intradural epidural hemolymphangioma: A case report
Shou-Feng Sun, Xue-Hua Wang, Yuan-Dong Shao, Department of Spine Surgery, Binzhou People’s Hospital, Binzhou 256600, Shandong Province, China
Ying-Ying Yuan, Department of Infectious Disease, Binzhou People’s Hospital, Binzhou 256600, Shandong Province, China
Author contributions: Sun SF reviewed the literature and contributed to manuscript drafting; Wang XH and Yuan YY were responsible for data collection and analysis; Shao YD was responsible for the revision of the manuscript; and all authors issued final approval for the version to be submitted.
Supported by The Natural Science Foundation of Shandong Province , No. ZR2022LZY001 ; The Shandong Province traditional Chinese medicine science and technology project , No. M-2022133 ; The Shandong medical and health science and technology development plan project , No. 202004071188 ; The Practical teaching reform and research project of Binzhou Medical College , No. SJJY201927 ; and The Scientific research project of Affiliated Hospital of Binzhou Medical College , No. BY2020KJ74 .
Informed consent statement: Informed written consent was obtained from the patient for publication of this report and any accompanying images.
Conflict-of-interest statement: The authors declare that they have no conflict of interest to disclose.
CARE Checklist (2016) statement: The authors have read the CARE Checklist (2016), and the manuscript was prepared and revised according to the CARE Checklist (2016).
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Yuan-Dong Shao, MD, Chief Doctor, Department of Spine Surgery, People's Hospital of Binzhou City, No. 515 Huanghe 7th Road, Bincheng District, Binzhou 256600, Shandong Province, China. syd201213@126.com
Received: April 23, 2024
Revised: May 28, 2024
Accepted: July 1, 2024
Published online: September 6, 2024
Processing time: 84 Days and 16.5 Hours
Revised: May 28, 2024
Accepted: July 1, 2024
Published online: September 6, 2024
Processing time: 84 Days and 16.5 Hours
Core Tip
Core Tip: This case report emphasizes the importance of accurate diagnosis using magnetic resonance imaging combined with patient history and pathology. Surgical resection is the most effective treatment for hemolymphangiomas, especially when their growth compresses surrounding tissues. Complete radical resection may be necessary to prevent recurrence. The risk of recurrence is low, and there have been no reports of malignant transformation.