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Extraskeletal myxoid chondrosarcoma of the leg in a child: A case report

RATIONALE: Extraskeletal myxoid chondrosarcoma is a slow-growing soft tissue tumor of adults with a propensity for local recurrence and eventual metastasis. Only 17 pediatric and adolescent cases have been reported. PATIENT CONCERNS: Here we present an 11-year-old boy with a 3-year history of a slow...

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Detalles Bibliográficos
Autores principales: Al Khader, Ali, Nsour, Esra, Al-Zubi, Raneem Bassam, Al Maadat, Hakam Mansor Dahar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6485760/
https://www.ncbi.nlm.nih.gov/pubmed/30985717
http://dx.doi.org/10.1097/MD.0000000000015207
Descripción
Sumario:RATIONALE: Extraskeletal myxoid chondrosarcoma is a slow-growing soft tissue tumor of adults with a propensity for local recurrence and eventual metastasis. Only 17 pediatric and adolescent cases have been reported. PATIENT CONCERNS: Here we present an 11-year-old boy with a 3-year history of a slowly growing painless left leg mass. Magnetic resonance imaging of the lesion revealed a subfascial well-circumscribed lesion with intramuscular extension in the medial gastrocnemius muscle of the left leg. DIAGNOSES: He underwent wide local excision of the mass and the histomorphological and immunohistochemical findings were consistent with extraskeletal myxoid chondrosarcoma. INTERVENTIONS: Possible radiotherapy was the further management plan. OUTCOMES: He was in good condition with no evidence of recurrence at 6 months postsurgery. LESSONS: Although pediatric cases of extraskeletal myxoid chondrosarcoma were reported to be aggressive, the tumor in this case demonstrated indolent behavior. Furthermore, the tumor in this case showed primitive round cell foci which adds to a previous study that especially reported this morphology in pediatric cases.