Multidisciplinary approach to orbital embryonic rhabdomyosarcoma: About a case.
Orbit
Orbita
Orbital rhabdomyosarcoma
Orbital tumor
Rabdomiosarcoma
Rabdomiosarcoma orbitario
Rhabdomyosarcoma
Tumor de orbita
Journal
Archivos de la Sociedad Espanola de Oftalmologia
ISSN: 2173-5794
Titre abrégé: Arch Soc Esp Oftalmol (Engl Ed)
Pays: Spain
ID NLM: 101715860
Informations de publication
Date de publication:
Oct 2021
Oct 2021
Historique:
received:
03
06
2020
accepted:
02
09
2020
entrez:
8
10
2021
pubmed:
9
10
2021
medline:
16
10
2021
Statut:
ppublish
Résumé
Of the head and neck tumoral lesions in children and adolescents, 5%-10% are primary malignant tumors. Among these tumors, orbital rhabdomyosarcoma stands out, which is the most common primary soft tissue sarcoma in children. Its diagnosis requires a high degree of clinical suspicion, and it can be corroborated with a series of examinations, in order to stage it and carry out the appropriate treatment. Currently, surgery and chemotherapy are the primary treatments, and the use of conventional radiotherapy is limited to cases where previous treatments fail or there is a risk of recurrence. The following case report aims to expose the clinical picture, diagnosis, staging and integral treatment of orbital rhabdomyosarcoma, as well as the interdisciplinary management that was performed to improve the patient's prognosis.
Identifiants
pubmed: 34620486
pii: S2173-5794(20)30253-X
doi: 10.1016/j.oftale.2020.09.005
pii:
doi:
Types de publication
Case Reports
Langues
eng
Sous-ensembles de citation
IM
Pagination
552-555Informations de copyright
Copyright © 2020 Sociedad Española de Oftalmología. Published by Elsevier España, S.L.U. All rights reserved.