• Home
  • Browse
    • Current Issue
    • By Issue
    • By Author
    • By Subject
    • Author Index
    • Keyword Index
  • Journal Info
    • About Journal
    • Aims and Scope
    • Editorial Board
    • Publication Ethics
    • Indexing and Abstracting
    • Peer Review Process
  • Guide for Authors
  • Submit Manuscript
  • Contact Us
 
  • Login
  • Register
Home Articles List Article Information
  • Save Records
  • |
  • Printable Version
  • |
  • Recommend
  • |
  • How to cite Export to
    RIS EndNote BibTeX APA MLA Harvard Vancouver
  • |
  • Share Share
    CiteULike Mendeley Facebook Google LinkedIn Twitter
Egyptian Journal of Ear, Nose, Throat and Allied Sciences
arrow Articles in Press
arrow Current Issue
Journal Archive
Volume Volume 26 (2025)
Volume Volume 25 (2024)
Volume Volume 24 (2023)
Issue Issue 24
Volume Volume 23 (2022)
Volume Volume 22 (2021)
Volume Volume 21 (2020)
Volume Volume 20 (2019)
Volume Volume 19 (2018)
Gabsi, O., Mejbri, M., Frikha, W., Idriss, S., Bechraoui, R., Mizouni, H., Beltaief, N. (2023). Child presenting with a huge cervicofacial mass: about a case report. Egyptian Journal of Ear, Nose, Throat and Allied Sciences, 24(24), 1-5. doi: 10.21608/ejentas.2023.216361.1644
Oumaima Gabsi; Maha Mejbri; Wassim Frikha; Sara Idriss; Rim Bechraoui; Habiba Mizouni; Najeh Beltaief. "Child presenting with a huge cervicofacial mass: about a case report". Egyptian Journal of Ear, Nose, Throat and Allied Sciences, 24, 24, 2023, 1-5. doi: 10.21608/ejentas.2023.216361.1644
Gabsi, O., Mejbri, M., Frikha, W., Idriss, S., Bechraoui, R., Mizouni, H., Beltaief, N. (2023). 'Child presenting with a huge cervicofacial mass: about a case report', Egyptian Journal of Ear, Nose, Throat and Allied Sciences, 24(24), pp. 1-5. doi: 10.21608/ejentas.2023.216361.1644
Gabsi, O., Mejbri, M., Frikha, W., Idriss, S., Bechraoui, R., Mizouni, H., Beltaief, N. Child presenting with a huge cervicofacial mass: about a case report. Egyptian Journal of Ear, Nose, Throat and Allied Sciences, 2023; 24(24): 1-5. doi: 10.21608/ejentas.2023.216361.1644

Child presenting with a huge cervicofacial mass: about a case report

Article 48, Volume 24, Issue 24, 2023, Page 1-5  XML PDF (302.32 K)
Document Type: Case report
DOI: 10.21608/ejentas.2023.216361.1644
View on SCiNiTO View on SCiNiTO
Authors
Oumaima Gabsi email 1; Maha Mejbri2; Wassim Frikha2; Sara Idriss2; Rim Bechraoui2; Habiba Mizouni2; Najeh Beltaief2
1Department of ENT and cervicofacial surgery Hospital of La Rabta Tunis
2ENT and maxillofacial Department, Radiology Department, La Rabta Hospital Tunis
Abstract
Introduction: Rhabdomyosarcoma (RMS) is a malignant mesenchymal neoplasm. It is one of the most common malignant head and neck tumors in children and the most frequent soft-tissue sarcoma. The main locations are the base of the skull and the nasopharynx. We present a rare case of a child presenting with parotid RMS.
Presentation of Case: A 4-year-old male was admitted to our hospital with the chief complaints of a progressively enlarging, cervicofacial swelling. There was no history of fever or any other constitutional symptoms. Physical examination revealed a 60 mm left cervicofacial swelling, trismus and grade IV left peripheral facial paralysis. There were no fever or palpable nodes. Biological findings showed an increased LDH. Computed tomography scan of the neck revealed a bulky tumor in the left cervicofacial region, involving both superficial and deep lobes of parotid gland, causing compression of oropharynx, extending to the left cervical lymph nodes measuring 77*55 mm with difficulties determining the starting point. Two days after his admission, he presented dyspnea and fever. A tracheotomy was performed associated to cervical biopsy under general anesthesia. The immunohistochemical analysis revealed intense positivity for desmin and myogenin favoring the diagnosis of embryonal rhabdomyosarcoma. The patient received chemotherapy and radiotherapy. A residual mass remained in the parotid region, in contact with the carotid artery. Tumor resection was discussed but ruled out due to high surgical risk.
Conclusion: Parotid RMS is a rare entity. Treatment follows a rigorous international protocol associating surgery, chemotherapy and radiation therapy.
Key Words: Children, embryonal rhabdomyosarcoma
Keywords
Children; embryonal rhabdomyosarcoma; malignant tumor; parotid gland
Main Subjects
Paediatric diseases and paediatric H&N oncology, Maxillofacial surgery.
Statistics
Article View: 389
PDF Download: 404
Home | Glossary | News | Aims and Scope | Sitemap
Top Top

Journal Management System. Designed by NotionWave.