Rare breast and subcutaneous metastases from pancreatic neuroendocrine tumor: a case report

Rare breast and subcutaneous metastases from pancreatic neuroendocrine tumor: a case report

Abstract Background Neuroendocrine tumors are a group of rare neoplasms, and the pancreatic neuroendocrine tumors (PNETs) represent only 1–2% of all pancreatic malignant tumors. The most common sites of these tumors include the gastrointestinal tract, lung, adrenal gland, and thyroid gland. Moreover...

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Bibliographic Details
Main Authors: Dorotea Bosco, Salvatore Perrotti, Corrado Spatola, Giada Maria Vecchio, Rosalia Latino, Antonio Di Cataldo
Format: Article
Language:English
Published: BMC 2019-07-01
Series:World Journal of Surgical Oncology
Subjects:
Pancreatic neuroendocrine tumors
Rare metastatic localization
Multiple metastases
Histological findings
Surgical treatment
Case report
Online Access:http://link.springer.com/article/10.1186/s12957-019-1662-0

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http://link.springer.com/article/10.1186/s12957-019-1662-0

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