Clinical-pathologic profile of head and neck rhabdomyosarcoma in children: a systematic review
This systematic review aimed to analyze the clinicopathological profile and relevant prognostic factors of head and neck rhabdomyosarcoma in pediatric patients. The search was carried out in the electronic search portals PubMed, Lilacs, Embase, Scopus, and Web of Science. The search yielded studies...
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Published in | Journal of the Korean Association of Oral and Maxillofacial Surgeons Vol. 49; no. 2; pp. 61 - 67 |
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Main Authors | , , |
Format | Journal Article |
Language | Korean |
Published |
대한구강악안면외과학회
30.04.2023
Korean Association Of Oral And Maxillofacial Surgeons |
Subjects | |
Online Access | Get full text |
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Abstract | This systematic review aimed to analyze the clinicopathological profile and relevant prognostic factors of head and neck rhabdomyosarcoma in pediatric patients. The search was carried out in the electronic search portals PubMed, Lilacs, Embase, Scopus, and Web of Science. The search yielded studies that were then analyzed regarding study topic, data extraction, and risk of bias using the STROBE (Strengthening the Reporting of Observational Studies) guidelines. Finally, three studies were included for qualitative analysis. Most of the cases involved embryonic and alveolar rhabdomyosarcoma. Expression of MYOD1 was highly correlated with diagnosis of spindle cell/sclerosing rhabdomyosarcoma, which appears to have a poor prognosis in children. Furthermore, tumor size <5 cm and absence of metastasis accompanied by complete resection and administration of adjuvant therapies such as chemotherapy and radiotherapy favored a better prognosis. |
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AbstractList | This systematic review aimed to analyze the clinicopathological profile and relevant prognostic factors of head and neck rhabdomyosarcoma in pediatric patients. The search was carried out in the electronic search portals PubMed, Lilacs, Embase, Scopus, and Web of Science. The search yielded studies that were then analyzed regarding study topic, data extraction, and risk of bias using the STROBE (Strengthening the Reporting of Observational Studies) guidelines. Finally, three studies were included for qualitative analysis. Most of the cases involved embryonic and alveolar rhabdomyosarcoma. Expression of MYOD1 was highly correlated with diagnosis of spindle cell/sclerosing rhabdomyosarcoma, which appears to have a poor prognosis in children. Furthermore, tumor size <5 cm and absence of metastasis accompanied by complete resection and administration of adjuvant therapies such as chemotherapy and radiotherapy favored a better prognosis. |
Author | Nelson Leonel Del Hierro Polanco Ludimila Lemes Moura Beatriz Della Terra Mouco Garrido |
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DocumentTitleAlternate | Clinical-pathologic profile of head and neck rhabdomyosarcoma in children: a systematic review |
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Keywords | Head and neck neoplasms MyoD1 myogenic differentiation protein Rhabdomyosarcoma Spindle cell rhabdomyosarcoma |
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TableOfContents | I. Introduction II. Materials and Methods III. Results IV. Discussion V. Conclusion ORCID Authors’ Contributions Funding Conflict of Interest References |
Title | Clinical-pathologic profile of head and neck rhabdomyosarcoma in children: a systematic review |
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