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A well differentiated, low grade neuroendocrine tumor (carcinoid tumor) that arises from the jejunum. The mitotic count is less than 2 per 10 HPF and/or the Ki67 index is equal to or less than 2 percent.
No clinical trials have been registered for jejunal neuroendocrine tumor G1.
6 publications have been identified in PubMed for jejunal neuroendocrine tumor G1. Research spans Clinical Trial Publication (33%), Epidemiology / Natural History (33%), and Review / Meta-Analysis (17%).
Can C (2026). [PMID: 41545070](https://pubmed.ncbi.nlm.nih.gov/41545070/). *Journal of nuclear medicine : official publication, Society of Nuclear Medicine*. [Case Report / Case Series]
Ocasio Quinones GA (2026). [PMID: 32809560](https://pubmed.ncbi.nlm.nih.gov/32809560/). *Unknown Journal*. [Review / Meta-Analysis]
Karges K (2025). [PMID: 40996947](https://pubmed.ncbi.nlm.nih.gov/40996947/). *Neuroendocrinology*. [Epidemiology / Natural History]
Suzuki K (2025). [PMID: 40433770](https://pubmed.ncbi.nlm.nih.gov/40433770/). *Veterinary surgery : VS*. [Clinical Trial Publication]
Tayyab Z (2025). [PMID: 40291327](https://pubmed.ncbi.nlm.nih.gov/40291327/). *Cureus*. [Epidemiology / Natural History]
Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 3:04 AM UTC
Romano E (2024). [PMID: 39064666](https://pubmed.ncbi.nlm.nih.gov/39064666/). *Nutrients*. [Clinical Trial Publication]