Yi An-Qi, Xie Guang-Hua
Department of Hepatobiliary Surgery, Yanbian University Affiliated Hospital, Yanji 133099, Jilin Province, China.
World J Gastrointest Oncol. 2025 Apr 15;17(4):100497. doi: 10.4251/wjgo.v17.i4.100497.
Pancreatic neuroendocrine neoplasms (pNENs) are rare, heterogeneous tumors accounting for 1%-2% of pancreatic tumors, with significant malignant potential. Intraductal papillary mucinous neoplasm of the bile duct (IPMN-B) is a rare precancerous lesion in the bile duct system, with potential for malignancy. The combination of pNENs and IPMN-B is exceptionally rare and often leads to misdiagnosis. This study aims to report a rare case of pNENs combined with IPMN-B treated at Yanbian University Hospital to improve understanding and management of this unusual tumor combination.
We retrospectively analyzed a case from Yanbian University Hospital. We reviewed clinical records, imaging findings, endoscopic retrograde cholangiopancreatography, surgical exploration, and histopathological examination. The patient was diagnosed with pNENs and IPMN-B. Surgical treatment was performed, with follow-up showing effective management and no significant recurrence.
This case represents the first report of pNENs combined with IPMN-B. It highlights the need for thorough diagnostic evaluation to prevent misdiagnosis and improve treatment strategies.
胰腺神经内分泌肿瘤(pNENs)是罕见的异质性肿瘤,占胰腺肿瘤的1%-2%,具有显著的恶性潜能。胆管内乳头状黏液性肿瘤(IPMN-B)是胆管系统中一种罕见的癌前病变,有恶变可能。pNENs与IPMN-B的合并极为罕见,常导致误诊。本研究旨在报告1例在延边大学附属医院接受治疗的pNENs合并IPMN-B的罕见病例,以提高对这种不寻常肿瘤组合的认识和处理能力。
我们回顾性分析了延边大学附属医院的1例病例。我们查阅了临床记录、影像学检查结果、内镜逆行胰胆管造影、手术探查及组织病理学检查。该患者被诊断为pNENs和IPMN-B。实施了手术治疗,随访显示治疗有效且无明显复发。
该病例是pNENs合并IPMN-B的首例报道。它强调了进行全面诊断评估以防止误诊并改进治疗策略的必要性。