EC Clinical and Medical Case Reports

Case Report Volume 8 Issue 4 - 2025

A Knee Synovial Sarcoma in a Child: A Case Report

Majda Ankri1*, Fatima Zohra Benbrahim1, Nazik Allali1, Latifa Chat1, Siham El Haddad1 and Leila Rouas2

1Pediatric Radiology Department, Children’s Hospital, University Mohammed V, Rabat, Morrocco

2Anatomopatholgy Department, Children’s Hospital, University Mohammed V, Rabat, Morrocco

*Corresponding Author: Majda Ankri, Pediatric Radiology Department, Children’s Hospital, University Mohammed V, Rabat, Morrocco.
Received: January 08, 2025; Published: March 13, 2025



Synovial sarcomas are rare malignant tumors of soft tissues, primarily occurring in young adults. They can develop in any soft tissue of the body but are more commonly found in the extremities near a major joint (lower two-thirds of the lower limbs). Other, albeit rare, originating sites include the head and neck, paravertebral region, chest, and abdominal wall. These tumors exhibit slow progression, marked by a gradual increase in mass volume, and are often painless. Surgical treatment involves mass resection, sometimes necessitating amputation of the entire limb. Adjuvant chemotherapy and/or radiotherapy are necessary to reduce the risk of local or distant recurrence. The recurrence rate depends primarily on the histological type of the tumor. We present the case of a patient operated for synovial sarcoma, who came for magnetic resonance imaging (MRI) of the lower limb following the discovery of osteocondensation in the femoral stump (operative site) on standard X-ray during postoperative surveillance.

 Keywords: Synovialosarcoma; MRI; Recidivism

Majda Ankri., et al. "A Knee Synovial Sarcoma in a Child: A Case Report." EC Clinical and Medical Case Reports 8.4 (2025): 01-07.