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A Mouse Model of Incompletely Resected Soft Tissue Sarcoma for Testing Neoadjuvant Therapies
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Metachronous Bilateral Extremity Soft Tissue Sarcomas.

Ghodratollah Nowrasteh1, Tanim Aziz1, Mohammed Al Assas2

  • 1Department of Surgery, Division of Surgical Oncology, Tawam Hospital, Al Ain, United Arab Emirates.

The American Journal of Case Reports
|January 9, 2016
PubMed
Summary

Bilateral soft tissue sarcomas (STS) are rare but indicate a poor prognosis. Early detection of these extremity tumors, including liposarcoma and leiomyosarcoma, is crucial for patient survival.

Area of Science:

  • Oncology
  • Surgical Pathology

Background:

  • Soft tissue sarcomas (STS) constitute 1% of adult cancers, predominantly affecting extremities.
  • Liposarcoma is the most frequent STS subtype, accounting for 20% of adult sarcomas.

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  • Etiology of STS is often uncertain, though risk factors include rare syndromes, chemical exposure, chemotherapy, and radiation.