Spontaneous Regression in Pancreatic Neuroendocrine Tumor
Spontaneous regression (SR) of pancreatic neuroendocrine tumors (pNETs) is extremely rare. We herein report a 64-year-old man with a nonfunctioning pNET that was incidentally detected during an evaluation for back pain. Imaging showed a 30-mm mass in the pancreatic tail, but surgery was delayed because of an old myocardial infarction. Four months later, follow-up imaging revealed tumor shrinkage of 20 mm without treatment. Laparoscopic distal pancreatectomy confirmed a grade 3 pNET. While ischemia was considered, factors such as mild immune response or metabolic stress may have contributed. This case suggests that ischemia and other factors may also play a role. Further research is needed to elucidate the mechanisms underlying SR in neuroendocrine tumors.
Authors
- Takeshi Matsumura (ORCID: https://orcid.org/0000-0002-4134-2635)
- Motoaki Bamba
- Yuki Yamauchi
Institutions
- Kyoto University (JP)
- Hyogo Prefectural Amagasaki General Medical Center (JP)
Publication Details
- Journal
- Internal Medicine
- Published
- 2025-07-16
- DOI
- https://doi.org/10.2169/internalmedicine.5837-25
- Primary Topic
- Neuroblastoma Research and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00