Right foot congenital infantile fibrosarcoma treated only with chemotherapy

Haci Ahmet Demir1, Canan Akyüz, Ali Varan

  • 1Department of Pediatric Oncology, Institute of Oncology, Hacettepe University, Ankara, Turkey. hdemir@hacettepe.edu.tr

Pediatric Blood & Cancer
|December 10, 2009
PubMed

Insights

Congenital infantile fibrosarcoma (CIF) is a rare pediatric tumor. A newborn treated with VAC chemotherapy avoided limb amputation and achieved normal walking function, showcasing a promising treatment outcome.

Area of Science:

  • Pediatric Oncology
  • Skeletal Tumors
  • Medical Imaging

Background:

  • Congenital infantile fibrosarcoma (CIF) is a rare pediatric soft tissue tumor.
  • While survival rates for CIF are generally high (84-93%), limb amputation remains a significant challenge.
  • Effective limb salvage strategies are crucial for improving quality of life in affected children.

Observation:

  • A male newborn presented with a rapidly growing mass in the right foot.
  • Radiographic and MRI evaluations indicated extensive destruction of tarsal, metatarsal, and phalangeal bones by the tumor.
  • The tumor's location and extent posed a high risk for limb loss.

Findings:

  • The patient received VAC chemotherapy (Vincristine, Actinomycin-D, Cyclophosphamide) as the sole treatment modality.
  • Following chemotherapy, the tumor regressed sufficiently to preserve limb function.
  • The child was able to walk normally, indicating successful limb salvage.

Implications:

  • This case highlights the potential efficacy of VAC chemotherapy in treating extensive congenital infantile fibrosarcoma of the foot.
  • Neoadjuvant chemotherapy may offer a viable alternative to amputation in select CIF cases.
  • Successful limb salvage through chemotherapy can significantly improve long-term functional outcomes and quality of life for pediatric patients with CIF.

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