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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.
No clinical trials have been registered for low-grade neuroendocrine tumor of the corpus uteri.
8 publications have been identified in PubMed for low-grade neuroendocrine tumor of the corpus uteri. Research spans Case Report / Case Series (63%), Review / Meta-Analysis (25%), and Other (13%).
Satala CB (2026). [PMID: 42196939](https://pubmed.ncbi.nlm.nih.gov/42196939/). *Diagnostics (Basel)*. [Review / Meta-Analysis]
Bode-Lesniewska B (2025). [PMID: 41073540](https://pubmed.ncbi.nlm.nih.gov/41073540/). *Virchows Arch*. [Case Report / Case Series]
Rikitake R (2025). [PMID: 40376725](https://pubmed.ncbi.nlm.nih.gov/40376725/). *Pathol Int*. [Review / Meta-Analysis]
Faridzi AS (2025). [PMID: 39819883](https://pubmed.ncbi.nlm.nih.gov/39819883/). *Am J Case Rep*. [Case Report / Case Series]
Yamamoto K (2025). [PMID: 40176851](https://pubmed.ncbi.nlm.nih.gov/40176851/). *Gynecol Oncol Rep*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 21, 2026, 4:54 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center
De Wispelaere N (2025). [PMID: 39854331](https://pubmed.ncbi.nlm.nih.gov/39854331/). *PLoS One*. [Other]
Jin P (2025). [PMID: 41305788](https://pubmed.ncbi.nlm.nih.gov/41305788/). *Medicine (Baltimore)*. [Case Report / Case Series]