Evidence map›Paper›PMID 40365345›Full record

ArticleFrontiers in oncology2025

A case report of rare pancreatic lymphoma: wide range of diffuse large B-cell lymphoma located in the body and tail of pancreas.

Xiang Song, Weiyu Hu, Li Zhang, Tao Mao, Yingli Zhu, Xiaokai Chen, Linlin Ren

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Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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7 authors.

Xiang SongDepartment of Gastroenterology, the Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Weiyu HuDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Li ZhangDepartment of Pathology, the Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Tao MaoDepartment of Gastroenterology, the Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Yingli ZhuDepartment of Gastroenterology, the Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Xiaokai ChenDepartment of Gastroenterology, the Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Linlin RenDepartment of Gastroenterology, the Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Pancreatic lymphoma is a rare pancreatic malignancy that is challenging to differentiate from diseases such as pancreatic cancer (PC). Although pathological examination of specimens obtained through surgery or endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) can aid in diagnosis, factors such as the occasional need for surgery and the variability in specimen quality from EUS-FNA complicate the diagnostic process. Misdiagnosis of pancreatic lymphoma as PC often leads to unnecessary surgery. In addition, surgical intervention may be necessary as a second-line treatment option for pancreatic lymphoma patients presenting with severe gastrointestinal symptoms. However, an optimal postoperative treatment strategy remains undefined, particularly in cases with extensive invasion, thereby impacting long-term survival. This lack of consensus underscores the need for further research to establish evidence-based therapeutic protocols. Case Description: We present the case of a 55-year-old patient (abdominal pain for over one month, intensified for two weeks). Imaging studies suggested a hypodense mass in the tail of the pancreas with ill-defined margins extending to the spleen, as well as a hypodense lesion within the spleen. The patient underwent surgical intervention, and postoperative pathological analysis confirmed the diagnosis of diffuse large B-cell lymphoma (DLBCL). Following surgery, the patient was initially treated with a short-term C2PET oral chemotherapy regimen, which was subsequently transitioned to the R-CHOP regimen. This therapeutic approach resulted in a favorable outcome, with the patient achieving a 5-year survival period. As far as we know, this may be the first reported case of pancreatic lymphoma with such a widespread involvement, in which patient underwent surgery and postoperative chemotherapy and obtained a 5-year survival period. Literature Review: We reviewed previously reported cases of the DLBCL pancreatic lymphoma located in the body and tail of pancreas, and conducted a comparative analysis. Purposes and Clinical Relevance: Our objectives are twofold: first, to highlight the critical role of preoperative EUS-FNA and positron emission tomography-computed tomography in the diagnostic evaluation for patients with pancreatic mass and suspected lesions in immune-associated organs; and second, to propose evidence-based recommendations for postoperative chemotherapy in cases of DLBCL involving the pancreas.

Indexed as

diagnosisdiffuse large B-cell lymphomapancreatic cancerpancreatic lymphomapostoperative chemotherapy

Identifiers

PMID40365345
PMCPMC12069054

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