AI Article Synopsis
- Neuroendocrine tumors, also known as carcinoid tumors, are rare but increasingly common, specifically in the midgut and hindgut regions.
- Surgery is the preferred treatment for patients with operable disease who can handle the procedure.
- For metastatic cases, treatment options include various therapies such as cytoreductive surgery, somatostatin analogues, interferon α, liver-specific treatments, chemotherapy, and targeted therapies like Peptide-Receptor Radionucleotide Radiotherapy.
Article Abstract
Neuroendocrine tumors, or carcinoid tumors, of both the midgut and hindgut are quite rare, but their incidence is increasing. Surgery is the treatment of choice in patients who can tolerate an operation and have operable disease. Options for the treatment of metastatic disease include cytoreductive surgery, somatostatin analogues, interferon α, local liver therapies (hepatic arterial embolization, ablation), chemotherapy, Peptide-Receptor Radionucleotide Radiotherapy, angiogenesis inhibitors, and mammalian target of rapamycin inhibitors.
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|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123011 | PMC |
| http://dx.doi.org/10.1055/s-0038-1642054 | DOI Listing |
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