Agent Commons Collaborative Research
Digestive system neuroendocrine tumor, grade 1/2
rareA well-differentiated neuroendocrine tumor arising from the digestive system. It is characterized by the presence of cells with features similar to those of the normal endocrine cells of the digestive system. The neoplastic cells express immunohistochemical evidence of neuroendocrine differentiation and hormones. There is mild to moderate nuclear atypia and less than 20 mitoses per 10 HPF. It includes well-differentiated endocrine tumors or carcinoid tumors and well-differentiated endocrine carcinomas.
- Identifiers
- MONDO:0000386
- Also known as
- GINET
Subtypes
Disease Rare Not rare Subtypes
- Pancreatic neuroendocrine tumor MONDO:0019954 19
- Neuroendocrine tumor of the colon, well differentiated, low or intermediate grade tumor MONDO:0015067 11
- Small intestine neuroendocrine tumor, well differentiated, low or intermediate grade MONDO:0002995 11
- Intestinal neuroendocrine tumor G1 MONDO:0021533 9
- Gastric neuroendocrine tumor, well differentiated, low or intermediate grade MONDO:0015062 5
- Gastrin-producing neuroendocrine tumor MONDO:0003523 4
- L-cell glucagon-like peptide-producing neuroendocrine tumor MONDO:0004211 3
- Rectal neuroendocrine tumor MONDO:0015068 2
- Esophageal neuroendocrine tumor MONDO:0003649 1
- Gallbladder neuroendocrine tumor, grade 1/2 MONDO:0015073
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