Soft-tissue sarcoma

Nathan F. Gilbert, Christopher P. Cannon, Patrick P. Lin, Valerae O. Lewis

Research output: Contribution to journalReview articlepeer-review

89 Scopus citations

Abstract

Soft-tissue sarcomas are rare malignancies of mesodermal origin. Common sites of involvement include the extremities, trunk, retroperitoneum, and the head and neck. Soft-tissue sarcomas of the extremities and pelvis are the most relevant to the orthopaedic surgeon. The patient with extremity soft-tissue sarcoma typically presents with a painless, enlarging mass. Advanced imaging techniques and biopsy, which are best done at tertiary referral centers, usually confirm the diagnosis. Factors such as sarcoma size, location, grade, histologic subtype, and stage, as well as patient age and comorbidities, determine the specific approach to management and patient outcome. Limb-sparing surgical resection is the mainstay of treatment. Radiation is used for unresectable tumors and as a neoadjuvant or an adjuvant to resection. The use of chemotherapy is controversial, and no standardized protocol has been established.

Original languageEnglish (US)
Pages (from-to)40-47
Number of pages8
JournalJournal of the American Academy of Orthopaedic Surgeons
Volume17
Issue number1
DOIs
StatePublished - Jan 2009

ASJC Scopus subject areas

  • Surgery
  • Orthopedics and Sports Medicine

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