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.

Insights

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.
Abstract