Non-rhabdomyosarcoma Soft Tissue Sarcoma of the Extremities in the Pediatric Population

Authors

Keywords:

Sarcoma, Soft tissue neoplasms, Adolescent, Lower extremity

Abstract

Introduction: Soft tissue sarcomas represent a small percentage of connective tissue tumors in pediatric patients and have a low incidence, with acceptable five-year survival rates, making them tumors in which early diagnosis influences patient prognosis.

Objective: To describe the case of an adolescent female patient with a soft tissue sarcoma of the lower limb.

Case report: An adolescent female patient with a soft tissue sarcoma of the lower limb received a delayed diagnosis, which ultimately compromised different layers of the skin. She required extensive resections.

Conclusions: This pathology may present a delay in diagnosis when it is confused with other entities in the early stages of the disease, which progressively compromises more tissues. For this reason, it should be part of the range of possibilities to be considered by the healthcare team.

Keywords: sarcoma; soft tissue neoplasms; adolescent; lower extremity.

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Author Biographies

Julián Eduardo Jaimes Salazar, Médico general universidad El Bosque, Bogotá, Colombia

Médico general

María José Ariza Lascarro, Medica general Universidad del Norte, Barranquilla, Colombia.

Médico general

Ricardo Galán Suárez, Universidad Militar Nueva Granada, Bogotá, Colombia

Cirujano plástico

References

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Published

2026-09-07

How to Cite

1.
Linares Restrepo F, Jaimes Salazar JE, Ariza Lascarro MJ, Galán Suárez R. Non-rhabdomyosarcoma Soft Tissue Sarcoma of the Extremities in the Pediatric Population. Revista Cubana de Ortopedia y Traumatologí­a [Internet]. 2026 Sep. 7 [cited 2026 Sep. 8];40. Available from: https://revortopedia.sld.cu/index.php/revortopedia/article/view/1066