Pancreatic Hemangioma Suspected of Neuroendocrine Tumor

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 thi...

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Bibliographic Details
Published inThe Korean journal of gastroenterology Vol. 76; no. 1; pp. 46 - 48
Main Authors Jeong, Mo Ah, Lee, Jun Kyu, Nam, Ji Hyung, Jang, Dong Kee, Lim, Yun Jeong, Lee, Jeong-Ju, Kim, Eo-Jin
Format Journal Article
LanguageEnglish
Published Jin Publishing & Printing Co 25.07.2020
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Summary: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.
ISSN:1598-9992
2233-6869
DOI:10.4166/kjg.2020.76.1.46