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A rare malignant neoplasm with skeletal muscle differentiation arising from the cervix.
No clinical trials have been registered for rhabdomyosarcoma of the cervix uteri.
25 publications have been identified in PubMed for rhabdomyosarcoma of the cervix uteri. Research spans Case Report / Case Series (72%), Review / Meta-Analysis (12%), and Other (8%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 18 | 72% |
Research summaries | 3 |
Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 5:41 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Other research | 2 | 8% |
Disease patterns and progression | 2 | 8% |
Kajal P (2026). [PMID: 41837097](https://pubmed.ncbi.nlm.nih.gov/41837097/). *Int J Surg Case Rep*. [Case Report / Case Series]
Mustapha A (2026). [PMID: 41783377](https://pubmed.ncbi.nlm.nih.gov/41783377/). *Gynecol Oncol Rep*. [Case Report / Case Series]
Kokash D (2026). [PMID: 41868466](https://pubmed.ncbi.nlm.nih.gov/41868466/). *Radiol Case Rep*. [Case Report / Case Series]
Wei XQ (2026). [PMID: 41822797](https://pubmed.ncbi.nlm.nih.gov/41822797/). *Case Rep Obstet Gynecol*. [Case Report / Case Series]
Zheng J (2026). [PMID: 40936284](https://pubmed.ncbi.nlm.nih.gov/40936284/). *J Gynecol Oncol*. [Epidemiology / Natural History]
Li S (2026). [PMID: 41695363](https://pubmed.ncbi.nlm.nih.gov/41695363/). *Front Oncol*. [Other]
Walpole S (2026). [PMID: 41277477](https://pubmed.ncbi.nlm.nih.gov/41277477/). *Clin Genet*. [Case Report / Case Series]
Gao X (2025). [PMID: 40683204](https://pubmed.ncbi.nlm.nih.gov/40683204/). *Int J Gynecol Cancer*. [Epidemiology / Natural History]
Sichinava IG (2025). [PMID: 40734299](https://pubmed.ncbi.nlm.nih.gov/40734299/). *Probl Endokrinol (Mosk)*. [Case Report / Case Series]
Li S (2025). [PMID: 40703554](https://pubmed.ncbi.nlm.nih.gov/40703554/). *Front Oncol*. [Case Report / Case Series]
AI-curated news mentioning rhabdomyosarcoma of the cervix uteri
Updated Feb 5, 2026
A case report highlights a rare instance of epithelioid and spindle cell rhabdomyosarcoma of the rib associated with a FUS-TFCP2 fusion. This adds to the understanding of genetic factors in this rare cancer subtype.