CONGENITAL RHABDOMYOSARCOMA: A RARE AXILLARY PRESENTATION
DOI:
https://doi.org/10.7439/ijbar.v3i3.422Abstract
Rhabdomyosarcoma (RMS) is a malignant mesenchymal neoplasm that exhibits striated muscle differentiation, the third most common soft tissue sarcoma of childhood accounting for over half of all cases of soft tissue sarcomas in children. Rhabdomyosarcoma (RMS) is extremely rare in neonate1-6. Only twelve percent rhabdomyosarcoma account in trunk7. We report a case of congenital rhabdomyosarcoma in axilla (pretreatment staging T1b N0 M0) with embronal histological subtype. Treatment included complete resection with safe surgical margin and standerd chemotherapy with VAC regimen. Key Messages: Though most of the trunk tumours are of alveolar histological subtype without metastasis but rarely congenital RMS of trunk can present with large masses with metastasis and embryonal histological subtype in newborn.Downloads
Download data is not yet available.
Downloads
Published
2012-03-31
Issue
Section
Case Report
License
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (SeeThe Effect of Open Access).
How to Cite
CONGENITAL RHABDOMYOSARCOMA: A RARE AXILLARY PRESENTATION. (2012). International Journal of Biomedical and Advance Research, 3(3), 212-214. https://doi.org/10.7439/ijbar.v3i3.422