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Infantile fibrosarcoma in a child: a case report
A Hashemi1, S Tefagh2, A Seifadini3
1Department of Pediatrics, Hematology, Oncology and Genetic Research Center, Shahid Sadoughi University of Medical Sciences Health Services, Yazd, Iran.
Iranian Journal of Pediatric Hematology and Oncology
|February 28, 2014
Summary
Infantile fibrosarcoma, a rare soft tissue tumor, can recur but has a good prognosis in children. Successful treatment involves surgery and chemotherapy, with metastasis being uncommon.
Area of Science:
- Pediatric Oncology
- Surgical Pathology
Background:
- Infantile fibrosarcoma is a rare pediatric soft tissue tumor, primarily affecting extremities.
- While histopathologically similar to adult forms, infantile fibrosarcoma exhibits a significantly better survival prognosis.
- Recurrence is common, but metastasis rates are low, especially in younger children.
Observation:
- A case report details a nine-year-old girl with a recurrent left hand mass.
- Pathological examination revealed sheets of spindle-shaped cells, indicative of infantile fibrosarcoma.
- The patient presented with a relapsing mass, necessitating intervention.
Findings:
- The diagnosis of infantile fibrosarcoma was confirmed through pathological findings.
- The patient received a combination of surgical intervention and chemotherapy.
- The treatment resulted in a successful outcome with tumor regression.
Implications:
- Infantile fibrosarcoma should be considered in the differential diagnosis of pediatric soft tissue masses.
- The condition generally has a favorable prognosis with uncommon distant metastasis.
- Surgery is the primary treatment, with chemotherapy and radiotherapy aiding in metastasis reduction.
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