Diagnosis of functioning pancreaticoduodenal neuroendocrine tumors

被引:14
|
作者
Imamura, Masayuki [1 ]
Nakamoto, Yuji [2 ]
Uose, Suguru [3 ]
Komoto, Izumi [1 ,4 ]
Awane, Masaaki [4 ]
Taki, Yoshiro [4 ]
机构
[1] Kansai Elect Power Hosp, Neuroendocrine Tumor Ctr, Fukushima Ku, Osaka 5530003, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Diagnost Imaging & Nucl Med, Kyoto, Japan
[3] Kansai Elect Power Hosp, Dept Gastroenterol, Fukushima Ku, Osaka 5530003, Japan
[4] Kansai Elect Power Hosp, Dept Surg, Fukushima Ku, Osaka 5530003, Japan
关键词
Functioning duodenal neuroendocrine tumor; Functioning pancreaticoduodenal neuroendocrine tumor; Gastrinoma; Insulinoma; ENDOCRINE NEOPLASIA TYPE-1; INJECTION TEST; EUS-FNA; PANCREAS; CELL; INSULINOMA; SURGERY; GASTRINOMA; MANAGEMENT; SECRETION;
D O I
10.1002/jhbp.209
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Functioning pancreaticoduodenal neuroendocrine tumors (PD-NETs) are popular in a textbook, but they are still unfamiliar to a general clinician, and delay of diagnosis or misdiagnosis has been reported even today. It is a consensus that sporadic functioning PD-NET is cured only by surgical resection. So, early detection and early resection is the gold standard for the treatment of functioning PD-NET. Functioning PD-NETs in patients with multiple endocrine neoplasia type 1 (MEN 1) are often multiple. You should check about MEN 1 whenever you encountered multiple PD-NET. They are diagnosed in younger age than sporadic cases. In most cases they are accompanied with numerous microscopic or macroscopic nonfunctioning P-NETs, which are potentially metastatic and the most common cause of death in MEN 1 patients. (c) Japanese Society of Hepato-Biliary-Pancreatic Surgery
引用
收藏
页码:602 / 609
页数:8
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