ArticleContemporary clinical dentistry
Rhabdomyosarcoma in a pediatric patient: A rare case report.
Article in Contemporary clinical dentistry. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.
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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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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
10 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.
- Rhabdomyosarcoma of the head and neck in pediatric patients: a systematic review.Medicina oral, patologia oral y cirugia bucal · 2022Pooled it
- A Report of Two Cases of Embryonal Rhabdomyosarcoma: Diagnostic Insights From Pathology.Cureus · 2025Article
- A Primary Intraosseous Rhabdomyosarcoma of Mandible: Report of a Rare Case and Review of Literature.Frontiers in dentistry · 2025Article
- Navigating Complexities in Pediatric Rhabdomyosarcoma: A Case Report on Its Neurological Implications.Cureus · 2023Article
- Rhabdomyosarcoma in the maxillary gingiva of a child patient.Journal of surgical case reports · 2021Article
- Rhabdomyosarcoma involving maxilla mimicking gingival enlargement: A diagnostic challenge.BMJ case reports · 2019Article
- Surgical Interventions for Advanced Parameningeal Rhabdomyosarcoma of Children and Adolescents.Cureus · 2018Review
- Embryonal rhabdomyosarcoma in the maxillary sinus with orbital involvement in a pediatric patient: Case report.World journal of clinical cases · 2017Article
- Embryonal rhabdomyosarcoma: A rare oral tumor.Journal of oral and maxillofacial pathology : JOMFPArticle
- Oral rhabdomyosarcoma in an adult male: A rare case report.Journal of oral and maxillofacial pathology : JOMFPArticle
Corrections and comments
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Rhabdomyosarcoma (RMS), a tumor of skeletal muscle origin, is the second most common soft tissue sarcoma encountered in childhood after osteosarcoma. The common sites of occurrence are the head and neck region, genitourinary tract, retroperitoneum, and to a lesser extent, the extremities. Site predilections in the oral cavity are a soft palate, maxillary sinus and alveolus, posterior mandibular region, cheek and lip, and possibly tongue. RMS is a highly malignant tumor with extensive local invasions and early hemorrhagic and lymphatic dissemination. Despite aggressive approaches incorporating surgery, dose-intensive combination chemotherapy, and radiation therapy, the outcome for patients with metastatic disease remains poor. Here, we report a case of oral RMS in a 1-year-old child and describe the clinical, radiological, histopathological, and immunohistochemical findings.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.