low-grade neuroendocrine tumor of the corpus uteri

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Disease Overview

Low-grade neuroendocrine tumor of the corpus uteri is an extremely rare uterine cancer typically characterized by a well demarcated, solid, frequently pedunculated tumor originating from neuroendocrine cells scattered within the endometrium, often associated with ectopic hormone production. Patients usually present with vaginal bleeding or discharge and a pelvic mass with a polypoid tumor sometimes protruding through the cervical canal. Symptoms related to ectopic hormone production (flushing, sweating, diarrhea, bronchospasm) may also develop.


Synonyms

  • low-grade neuroendocrine tumor of the uterine corpus
  • low-grade neuroendocrine tumour of the uterine corpus
  • well-differentiated neuroendocrine neoplasm of the endometrium
  • well-differentiated neuroendocrine tumor of the corpus uteri
  • well-differentiated neuroendocrine tumor of the endometrium
  • well-differentiated neuroendocrine tumour of the corpus uteri
  • well-differentiated neuroendocrine tumour of the endometrium

GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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Orphanet

Orphanet has a summary about this condition that may include information on the diagnosis, care, and treatment as well as other resources. Some of the information and resources are available in languages other than English. The summary may include medical terms, so we encourage you to share and discuss this information with your doctor. Orphanet is the French National Institute for Health and Medical Research and the Health Programme of the European Union.

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