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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
Journal Title
The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi
Volume
76
Number
1
Start Page
46
End Page
48
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/7080
DOI
10.4166/kjg.2020.76.1.46
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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