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Pancreatic Hemangioma Suspected of Neuroendocrine Tumoropen access
- Authors
- Jeong, M.A.; Lee, J.K.; Nam, J.H.; Jang, D.K.; Lim, Y.J.; Lee, J.-J.; Kim, E.-J.
- Issue Date
- Jul-2020
- Publisher
- NLM (Medline)
- Keywords
- Hemangioma; Neuroendocrine tumors; Pancreas
- Citation
- The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi, v.76, no.1, pp 46 - 48
- Pages
- 3
- Indexed
- SCOPUS
KCI
- Volume
- 76
- Number
- 1
- Start Page
- 46
- End Page
- 48
- ISSN
- 1598-9992
2233-6869
- Abstract
- Adult pancreatic hemangioma is an extremely rare disease, with only 22 cases reported since 1939. Pancreatic hemangioma has no specific symptoms, diagnostic imaging, or laboratory findings, making it difficult to be clinically suspected and diagnosed. The majority are confirmed after surgery. In this report, a 61-year-old woman presented with melena and showed multiple small hyper-vascular lesions in the pancreas. A pancreatic neuroendocrine tumor was suspected, and the patient underwent a distal pancreatectomy. The pathology examination and immunohistochemical study revealed a pancreatic hemangioma.
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Related Researcher
- Lim, Yun Jeong
- Graduate School (Department of Medicine)