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Nonfunctional pancreatic neuroendocrine tumours misdiagnosed as autoimmune pancreatitis:A case report and review of literature 被引量:1
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作者 Zi-Qi Lin Xin Li +4 位作者 Yan Yang Yi Wang Xiao-Ying Zhang Xiao-Xin Zhang Jia Guo 《World Journal of Clinical Cases》 SCIE 2022年第15期4886-4894,共9页
BACKGROUND Nonfunctional pancreatic neuroendocrine tumours are difficult to diagnose in the early stage of disease due to a lack of clinical symptoms,but they can rarely manifest as autoimmune pancreatitis.Autoimmune ... BACKGROUND Nonfunctional pancreatic neuroendocrine tumours are difficult to diagnose in the early stage of disease due to a lack of clinical symptoms,but they can rarely manifest as autoimmune pancreatitis.Autoimmune pancreatitis is an uncommon disease that may cause recurrent acute pancreatitis and is therefore often regarded as a special type of chronic pancreatitis.CASE SUMMARY We report a case of a 42-year-old female who had nonspecific upper abdominal pain for 4 years and radiological abnormalities of the pancreas that mimicked autoimmune pancreatitis.The symptoms and pancreatic imaging did not improve following 1 year of steroid therapy.Finally,pancreatic biopsy was performed through endoscopic ultrasonography-guided fine-needle aspiration biopsy,and nonfunctional pancreatic neuroendocrine tumours were ultimately diagnosed.Pancreatectomy has resolved her symptoms.CONCLUSION Therefore,the differentiation of nonfunctional pancreatic neuroendocrine tumours from autoimmune pancreatitis is very important,although it is rare.We propose that endoscopic ultrasonography-guided fine-needle aspiration biopsy should be performed if imaging characteristics are equivocal or the diagnosis is in question. 展开更多
关键词 pancreatic neuroendocrine tumour Nonfunctional pancreatic neuroendocrine tumour Autoimmune pancreatitis Endoscopic ultrasonography-guided fine needle aspiration biopsy Case report
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Octreotide acetate long-acting release in treatment of pancreatic neuroendocrine tumors 被引量:6
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作者 ZHANG Shi LI Yu-xiu LI Nai-shi LI Wen-hui ZHU Hui-juan GU Feng WANG Heng 《Chinese Medical Journal》 SCIE CAS CSCD 2009年第13期1582-1584,共3页
Pancreatic neuroendocrine tumours are uncommon neoplasms of the pancreas, accounting for around 2% of all primary pancreatic tumors. This specific group of tumours includes insulinoma, gastrinoma, glucagonoma, VIPoma,... Pancreatic neuroendocrine tumours are uncommon neoplasms of the pancreas, accounting for around 2% of all primary pancreatic tumors. This specific group of tumours includes insulinoma, gastrinoma, glucagonoma, VIPoma, somatostatinoma and others. They may cause a clinical syndrome due to hormone overproduction. These tumours tend to be less aggressive than pancreatic adenocarcinoma, however, more than 50% of them have metastasized to the liver at the time of diagnosis. Under this circumstance, surgery is impossible to resect all metastases. Thus other various medical measures have been explored in the treatment of these tumors. 展开更多
关键词 pancreatic neuroendocrine tumours GLUCAGONOMA GASTRINOMA octreotide acetate
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