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A rare case of Ewing's sarcoma of the maxillary sinus

Ewing's sarcoma is generally an aggressive, poorly differentiated bone and soft tissue tumor affecting children and young adults, it accounts for 4%-6% of all primary bone tumors and primary facial locations occur in only 1%-4% of all cases, primarily in the mandible and calvaria. Involvement o...

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Published in:Radiology case reports 2023-12, Vol.18 (12), p.4248-4252
Main Authors: Cherraqi, Amine, El Mandour, Jihane, Dghoughi, Basma, Tbouda, Mohammed, El Kababri, Maria, Hessissen, Laila, El Haddad, Siham, Allali, Nazik, Chat, Latifa
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container_title Radiology case reports
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creator Cherraqi, Amine
El Mandour, Jihane
Dghoughi, Basma
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El Kababri, Maria
Hessissen, Laila
El Haddad, Siham
Allali, Nazik
Chat, Latifa
description Ewing's sarcoma is generally an aggressive, poorly differentiated bone and soft tissue tumor affecting children and young adults, it accounts for 4%-6% of all primary bone tumors and primary facial locations occur in only 1%-4% of all cases, primarily in the mandible and calvaria. Involvement of the paranasal sinuses is rare. Here we report the case of an 11-year-old girl with no medical, surgical, or traumatic history, who presented for 1 month and progressive evolution of swelling of the left cheek, associated with pain, nasal obstruction, rhinorrhea, and a slight weight loss not quantified. A craniofacial computed tomography (CT) scan showed a mixed lytic and condensing lesional tissue process centered on the left maxillary sinus, heterogeneously enhanced after contrast injection, lysing the walls of the sinus extended to the homolateral nasal cavity and slightly infiltrating the adjacent soft tissues. An incisional biopsy was performed and the pathological study proved that it was Ewing's sarcoma. She was put on neoadjuvant chemotherapy using 6 courses of vincristine, doxorubicin, ifosfamide, etoposide which resulted in a partial regression of the tumor size by 50%. Then the patient was put on combined chemotherapy and radiotherapy. A follow-up CT scan after 6 courses of vincristine, actinomycin, cyclophosphamide, and 17 sessions of radiotherapy showed lesion stability. Maxillary Ewing's sarcoma is a rare and aggressive tumor. Therefore, early diagnosis, combination therapy, and long-term follow-up are suggested in such cases to improve the survival rate.
doi_str_mv 10.1016/j.radcr.2023.08.095
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subjects Case Report
Diagnosis
Ewing's sarcoma
Imaging
Maxillary sinus
Oncology
title A rare case of Ewing's sarcoma of the maxillary sinus
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