ReviewAutopsy & case reports2023
Embryonal rhabdomyosarcoma of the uterine cervix in an adult female.
Review in Autopsy & case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
8 citing papers in PubMed.
- Adult cervical embryonal rhabdomyosarcoma: a literature review of 41 adult cases with an illustrative aggressive case.Gynecologic oncology reports · 2026Article
- Symptom triad of primary cervical rhabdomyosarcomas as seen in a Nigerian tertiary hospital: A case series.Gynecologic oncology reports · 2026Article
- Article
- Case Report: Clinical analysis and literature review of two cases of high-grade adult-type cervical embryonal rhabdomyosarcoma.Frontiers in oncology · 2026Article
- Targeted maintenance therapy for a young woman with cervical rhabdomyosarcoma: A case report and review of literature.World journal of clinical oncology · 2025Article
- Cervical Rhabdomyosarcoma: A Case Report.Cureus · 2025Article
- Pleomorphic rhabdomyosarcoma of the vagina: A case report.World journal of clinical cases · 2024Article
- Patient-derived organoids facilitating individual therapy in an adolescent with embryonal rhabdomyosarcoma of the cervix: a case report and literature review.Frontiers in oncology · 2023Article
Corrections and comments
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Embryonal rhabdomyosarcoma (RMS) of the female genital tract is an uncommon malignancy, presenting mainly in the pediatric and adolescent populations, primarily affecting the first two decades of life. This malignancy presentation in adulthood is rare and is seldom seen. The incidence of this tumor affecting adult females is approximately 0.4 - 1%, with the common site being the vagina. This tumor infrequently involves the cervix. RMS has a poor survival rate and once diagnosed, it requires aggressive management by radical surgery accompanied by chemoradiation. We present a case of an anaplastic variant of embryonal RMS of the uterine cervix presenting as a cervical polyp in a 36-year-old female who complained of dyspareunia and post-coital bleeding.
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Registered trials
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