Abstract #837: Case Report: Effectivness of Medical Therapy with Octreotide in Men-1 Patient with Non-Funtional Pancreatic Neuroendocrine Tumor (NET)

2015 ◽  
Vol 21 ◽  
pp. 165-166
Author(s):  
Vinh Mai ◽  
Patrick Clyde ◽  
Mohammed Shakir
Keyword(s):  
Case Report ◽  
Neuroendocrine Tumor ◽  
Medical Therapy ◽  
Pancreatic Neuroendocrine Tumor ◽  
Men 1

Pancreatic neuroendocrine tumor and ileal carcinoid in acromegaly. Pluriglandular association in non-men 1 patient: A case report

Pancreatology ◽  
2014 ◽  
Vol 14 (3) ◽  
pp. S80-S81
Author(s):  
Valbona Liço ◽  
Anna Caterina Milanetto ◽  
Lucia Moletta ◽  
Carla Scaroni ◽  
Rita Alaggio ◽  
...  
Keyword(s):  
Case Report ◽  
Neuroendocrine Tumor ◽  
Pancreatic Neuroendocrine Tumor ◽  
Men 1 ◽  
Ileal Carcinoid

Case report: Refractory hypercalcemia due to a pancreatic neuroendocrine tumor misdiagnosed as adenocarcinoma

2020 ◽  
Author(s):  
Mirella Hage ◽  
Ségolène Hescot ◽  
Amani Asnacios ◽  
Sophia Bakopoulou ◽  
Laure Cazabat ◽  
...  
Keyword(s):  
Case Report ◽  
Neuroendocrine Tumor ◽  
Pancreatic Neuroendocrine Tumor

scholarly journals Pancreatic cystadenoma coexistent with incidental neuroendocrine tumor: a case report and literature review

2020 ◽  
Author(s):  
Jingjin Wu ◽  
Li Zhang ◽  
Zhiyong Yu
Keyword(s):  
Case Report ◽  
Neuroendocrine Tumor ◽  
Clinical Characteristics ◽  
Pancreatic Neuroendocrine Tumor ◽  
Interesting Case ◽  
Malignant Potential ◽  
The Other ◽  
Ultrasound Guided ◽  
Case Presentation ◽  
Pancreatic Cystadenoma

Abstract Background Pancreatic cystadenoma coexistent with neuroendocrine tumor is a rare disease which is reported sporadically. Case Presentation We herein present one such interesting case in a 67-year old man. There was only one mass detected preoperatively by different examinations. Endoscopic ultrasound-guided biopsy indicated a pancreatic neuroendocrine tumor. Therefore, a distal pancreatectomy was performed and the final histopathology revealed two separate masses in the pancreas, one was serious cystadenoma and the other neuroendocrine tumor. Conclusions SCA coexistent with PNET is rarely found during clinical practice. The component of PNET may not be confirmed until the operation. Based on the recorded cases, the malignant potential, clinical characteristics, treatment, and prognosis are remaining further researches.

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