Indication
Nonfunctional neuroendocrine tumor of gastrointestinal origin
A nonfunctional neuroendocrine tumor of gastrointestinal origin is an epithelial neoplasm arising from enterochromaffin or other neuroendocrine cells within the digestive tract, most commonly the small intestine, appendix, stomach, or rectum. Read more about Nonfunctional neuroendocrine tumor of gastrointestinal origin
7 drugs 7 manufacturers
Drugs that treat it
Common Nonfunctional neuroendocrine tumor of gastrointestinal origin therapies.
TORPENZ (everolimus)
EVEROLIMUS
EVEROLIMUS
AFINITOR (everolimus)
EVEROLIMUS
YULITHIRA (everolimus)
News & literature
Coming soonRelated codes
Coming soonRelated conditions & guidelines
Coming soonA nonfunctional neuroendocrine tumor of gastrointestinal origin is an epithelial neoplasm arising from enterochromaffin or other neuroendocrine cells within the digestive tract, most commonly the small intestine, appendix, stomach, or rectum.
Unlike functional neuroendocrine neoplasms, these tumors do not cause clinical hypersecretion syndromes—such as carcinoid syndrome—because they either produce biologically inactive substances or do not release vasoactive peptides and hormones in quantities sufficient to elicit systemic endocrine symptoms.
Patients are predominantly adults, and because hormonal clues are absent, tumors often follow an indolent early course and are discovered incidentally or at an advanced stage.
Clinical manifestations typically stem from local mass effect, mucosal ulceration, or distant metastases, presenting with nonspecific gastrointestinal symptoms such as abdominal pain, bowel obstruction, bleeding, or palpable hepatomegaly.
- nih.gov
A nonfunctional neuroendocrine tumor of gastrointestinal origin is an epithelial neoplasm arising from enterochromaffin or other neuroendocrine cells within the digestive tract, most commonly the small intestine, appendix, stomach, or rectum Patients are predominantly adults, and because hormonal clues are absent, tumors often follow an indolent early course and are discovered incidentally or at an advanced stage
- clevelandclinic.org
A nonfunctional neuroendocrine tumor of gastrointestinal origin is an epithelial neoplasm arising from enterochromaffin or other neuroendocrine cells within the digestive tract, most commonly the small intestine, appendix, stomach, or rectum
- nih.gov
Unlike functional neuroendocrine neoplasms, these tumors do not cause clinical hypersecretion syndromes—such as carcinoid syndrome—because they either produce biologically inactive substances or do not release vasoactive peptides and hormones in quantities sufficient to elicit systemic endocrine symptoms
- nih.gov
Unlike functional neuroendocrine neoplasms, these tumors do not cause clinical hypersecretion syndromes—such as carcinoid syndrome—because they either produce biologically inactive substances or do not release vasoactive peptides and hormones in quantities sufficient to elicit systemic endocrine symptoms Clinical manifestations typically stem from local mass effect, mucosal ulceration, or distant metastases, presenting with nonspecific gastrointestinal symptoms such as abdominal pain, bowel obst...
- nih.gov
Patients are predominantly adults, and because hormonal clues are absent, tumors often follow an indolent early course and are discovered incidentally or at an advanced stage Clinical manifestations typically stem from local mass effect, mucosal ulceration, or distant metastases, presenting with nonspecific gastrointestinal symptoms such as abdominal pain, bowel obstruction, bleeding, or palpable hepatomegaly
- cancer.org
Clinical manifestations typically stem from local mass effect, mucosal ulceration, or distant metastases, presenting with nonspecific gastrointestinal symptoms such as abdominal pain, bowel obstruction, bleeding, or palpable hepatomegaly
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