Sarcoma
- PMID: 30137818
- Bookshelf ID: NBK519533
Sarcoma
Excerpt
Soft tissue sarcomas (STS) are a group of more than 60 different neoplasms that can originate from any location throughout the human body and affect individuals at the extremes of age. From skeletal muscle, adipose tissue, blood, and lymphatics to connective tissue and peripheral nerves, these neoplasms can span a range of clinical presentations from benign lipomas to aggressive metastatic angiosarcomas. The real challenge in diagnosing these conditions is that several non-neoplastic conditions mimic STS. Soft tissue sarcomas are separated categorically as trunk and extremity from retroperitoneum. The majority of STS occurs spontaneously. However, germline mutations, radiation, and environmental exposure(s) have been causative.
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Sections
- Continuing Education Activity
- Introduction
- Etiology
- Epidemiology
- Pathophysiology
- History and Physical
- Evaluation
- Treatment / Management
- Differential Diagnosis
- Surgical Oncology
- Radiation Oncology
- Medical Oncology
- Staging
- Prognosis
- Complications
- Postoperative and Rehabilitation Care
- Deterrence and Patient Education
- Enhancing Healthcare Team Outcomes
- Review Questions
- References
References
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- Kondo T. Current Status of Proteomics in Ewing's Sarcoma. Proteomics Clin Appl. 2019 May;13(3):e1700130. - PubMed
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