Pediatric Extra-skeletal Sinonasal Ewing's Sarcoma: Report of Two Cases with Literature Review.
Ewing’s sarcoma
Extraskeletal
Pediatric
Sinonasal tumors
Journal
Indian journal of surgical oncology
ISSN: 0975-7651
Titre abrégé: Indian J Surg Oncol
Pays: India
ID NLM: 101532448
Informations de publication
Date de publication:
Sep 2024
Sep 2024
Historique:
received:
11
01
2024
accepted:
13
05
2024
pmc-release:
01
09
2025
medline:
27
9
2024
pubmed:
27
9
2024
entrez:
27
9
2024
Statut:
ppublish
Résumé
Ewing's sarcoma is a malignant small round cell tumor that belongs to the primitive class of neuroectodermal tumors. Ewing's sarcoma generally arises in the long bones of the extremities, and sinonasal localization of Ewing's sarcoma in pediatric population is an extremely rare event. The combination of histopathological examination and ancillary methods is extremely important to establish the diagnosis of Ewing's sarcoma. The treatment for Ewing's sarcoma includes a multidisciplinary approach with surgery, radiotherapy, and chemotherapy. Through this report, we try to communicate our experience and highlight the challenges encountered in diagnosing and approaching two extremely rare cases of pediatric sinonasal Ewing's sarcoma.
Identifiants
pubmed: 39328738
doi: 10.1007/s13193-024-01974-2
pii: 1974
pmc: PMC11422305
doi:
Types de publication
Case Reports
Journal Article
Langues
eng
Pagination
400-407Informations de copyright
© The Author(s), under exclusive licence to Indian Association of Surgical Oncology 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
Déclaration de conflit d'intérêts
Competing InterestsThe authors declare no competing interests.