When to Operate and What Are the Consequences of a Surgical Resection of a Neuroendrocine Tumour in the Pancreas or Small Bowel

被引:0
|
作者
Hain, E. [1 ,2 ]
Gharios, J. [1 ]
Sindayigaya, R. [1 ]
Gaujoux, S. [1 ,2 ]
机构
[1] AP HP, Serv Chirurg Pancreat & Endocrinienne, Hop Cochin, 27 Rue Faubourg St Jacques, F-75679 Paris 14, France
[2] Univ Paris 05, Paris, France
关键词
Neuroendocrine tumor; Pancreatectomy; Exocrine pancreatic insufficiency; Endocrine pancreatic insufficiency; Short bowel syndrome; Mesenteric lymphadenectomy; INTESTINAL NEUROENDOCRINE TUMORS; PROGNOSTIC-FACTORS; LYMPH-NODE; METASTASES; SURVIVAL; SURGERY;
D O I
10.3166/onco-2019-0048
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Neuroendocrine tumors (NET) are rare and can occur in all parts of the digestive tract. They can be functional or non-functional. All patients presenting NET should be discussed for the surgical management within the RENA-TEN tumor board. For sporadic pancreatic NET, surgery is recommended for non-functional lesion >2 cm in size and/or associated with ductal dilatation. For non-aggressive tumor, parenchyma-sparing surgery should be preferred to avoid exocrine and endocrine pancreatic insufficiency. For small bowel NET, surgery must always be considered to avoid complications such as small bowel obstruction. Lymphade-nectomy must include at least 8 noded. Surgery must avoid short bowel syndrome.
引用
收藏
页码:91 / 96
页数:6
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