Jia ZD, Zhang CY, Liang SZ, Li HL. Primary splenic histiocytic sarcoma: A case report and review of literature. World J Clin Cases 2026; 14(3): 116125 [DOI: 10.12998/wjcc.v14.i3.116125]
Corresponding Author of This Article
Hai-Liang Li, MD, Director, Department of Colorectal and Anal Surgery, The First People’s Hospital of Zunyi, The Third Affiliated Hospital of Zunyi Medical University, No. 98 North Fenghuang Road, Huichuan District, Zunyi 563099, Guizhou Province, China. lihailiang5612@163.com
Research Domain of This Article
Oncology
Article-Type of This Article
Case Report
Open-Access Policy of This Article
This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (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: http://creativecommons.org/licenses/by-nc/4.0/
Jan 26, 2026 (publication date) through Jan 23, 2026
Times Cited of This Article
Times Cited (0)
Journal Information of This Article
Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Share the Article
Jia ZD, Zhang CY, Liang SZ, Li HL. Primary splenic histiocytic sarcoma: A case report and review of literature. World J Clin Cases 2026; 14(3): 116125 [DOI: 10.12998/wjcc.v14.i3.116125]
World J Clin Cases. Jan 26, 2026; 14(3): 116125 Published online Jan 26, 2026. doi: 10.12998/wjcc.v14.i3.116125
Primary splenic histiocytic sarcoma: A case report and review of literature
Zhi-Dong Jia, Cheng-Yan Zhang, Sheng-Zhi Liang, Hai-Liang Li
Zhi-Dong Jia, Department of Hepatobiliary Surgery, Guangzhou Overseas Chinese Hospital, The First Affiliated Hospital of Jinan University, Guangzhou 510630, Guangdong Province, China
Cheng-Yan Zhang, Department of Laboratory, Clifford Hospital, Guangzhou 511495, Guangdong Province, China
Sheng-Zhi Liang, Department of General Surgery, The Affiliated Shunde Hospital of Jinan University, Foshan 528000, Guangdong Province, China
Hai-Liang Li, Department of Colorectal and Anal Surgery, The First People’s Hospital of Zunyi, The Third Affiliated Hospital of Zunyi Medical University, Zunyi 563099, Guizhou Province, China
Co-first authors: Zhi-Dong Jia and Cheng-Yan Zhang.
Author contributions: Jia ZD and Zhang CY wrote the main manuscript, and they contributed equally to this manuscript and are co-first authors; Jia ZD and Li HL revised the final manuscript; Liang SZ assisted with information research, data collection, and icon creation. All authors have read and approved the final manuscript.
Supported by the Science and Technology Projects in Guangzhou, No. 202201010653; Guangdong Provincial Medical Science and Technology Research Fund, No. A2021200; and Jinan University Medical Collaborative Fund, No. MF220209.
Informed consent statement: Informed written consent was obtained from the patient for publication of this report and any accompanying images.
Conflict-of-interest statement: All the authors report no relevant conflicts of interest for this article.
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: Hai-Liang Li, MD, Director, Department of Colorectal and Anal Surgery, The First People’s Hospital of Zunyi, The Third Affiliated Hospital of Zunyi Medical University, No. 98 North Fenghuang Road, Huichuan District, Zunyi 563099, Guizhou Province, China. lihailiang5612@163.com
Received: November 3, 2025 Revised: December 13, 2025 Accepted: January 6, 2026 Published online: January 26, 2026 Processing time: 80 Days and 15 Hours
Abstract
BACKGROUND
Histiocytic sarcoma (HS) is a rare lymphohematopoietic malignancy with nonspecific clinical manifestations, diagnostic challenges, high aggressiveness, and a poor prognosis. Primary HSs arising in the spleen are extremely uncommon, with few cases reported globally. Here, we present the clinical course of a patient with splenic HS.
CASE SUMMARY
A 67-year-old woman was admitted to our hospital because of a large splenic mass that was detected during a routine health examination 1 month before presentation. Abdominal computed tomography revealed a large occupying lesion in the spleen, which was possibly a lymphangioma. The patient underwent splenectomy, and postoperative pathological examination confirmed the diagnosis of splenic HS. At the 6-month telephonic follow-up, the patient reported feeling well.
CONCLUSION
Given the paucity of cases and the poor prognosis of splenic HS, whose definitive diagnosis hinges exclusively on pathology, and given that all current therapeutic strategies are based on isolated case reports, it is imperative to enhance our understanding of this disease to improve patient diagnosis and management.
Core Tip: Splenic histiocytic sarcoma (HS) is a rare lymphohematopoietic malignancy with nonspecific clinical manifestations, diagnostic challenges, high aggressiveness, and a poor prognosis. A 67-year-old woman was found to have a large splenic mass during a routine physical examination 1 month before presentation. After multidisciplinary discussion, laparoscopic splenectomy was recommended. The pathological findings were most compatible with the diagnosis of HS. A 6-month postoperative telephonic follow-up revealed that the patient felt well. Despite the poor prognosis, HS remains treatable. Early and definitive diagnosis based on pathology is required to optimize treatment.