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Classification and external resources
ICD-O: M8800/3
MeSH D012509

A sarcoma (from the Greek σάρξ sarx meaning "flesh") is a cancer that arises from transformed cells of mesenchymal origin. Thus, malignant tumors made of cancerous bone, cartilage, fat, muscle, vascular, or hematopoietic tissues are, by definition, considered sarcomas. This is in contrast to a malignant tumor originating from epithelial cells, which are termed carcinoma. Human sarcomas are quite rare. Common malignancies, such as breast, colon, and lung cancer, are almost always carcinoma.


File:Nibib 030207 105309 sarcoma.jpg

Optical Coherence Tomography (OCT) image of a sarcoma


Sarcomas are given a number of different names based on the type of tissue that they most closely resemble. For example, osteosarcoma resembles bone, chondrosarcoma resembles cartilage, liposarcoma resembles fat, and leiomyosarcoma resembles smooth muscle.


In addition to being named based on the tissue of origin, sarcomas are also assigned a grade (low, intermediate, or high) based on the presence and frequency of certain cellular and subcellular characteristics associated with malignant biological behavior. Low grade sarcomas are usually treated surgically, although sometimes radiation therapy or chemotherapy are used. Intermediate and high grade sarcomas are more frequently treated with a combination of surgery, chemotherapy and/or radiation therapy.[1] Since higher grade tumors are more likely to undergo metastasis (invasion and spread to locoregional and distant sites), they are treated more aggressively. The recognition that many sarcomas are sensitive to chemotherapy has dramatically improved the survival of patients. For example, in the era before chemotherapy, long term survival for patients with localized osteosarcoma was only approximately 20%, but now has risen to 60–70%.[2]


(ICD-O codes are provided, where available, along with the relevant edition.)

  • Askin's tumor (8803/3)
  • Sarcoma botryoides
  • Chondrosarcoma (9220/3-9240/3)
  • Ewing's (9260/3) — PNET (9473/3)
  • Malignant Hemangioendothelioma (9130/3)
  • Malignant Schwannoma (9560/3-9561/3)
  • Osteosarcoma (9180/3-9190/3)
  • Soft tissue sarcomas, including:
    • Alveolar soft part sarcoma (9581/3)
    • Angiosarcoma (9120/3)
    • Cystosarcoma Phyllodes
    • Dermatofibrosarcoma protuberans (DFSP) (8832/3-8833/3)
    • Desmoid Tumor (8821/1-8822/1)
    • Desmoplastic small round cell tumor (8806/3)
    • Epithelioid Sarcoma (8804/3)
    • Extraskeletal chondrosarcoma (9220/3)
    • Extraskeletal osteosarcoma (9180/3)
    • Fibrosarcoma (8810/3)
    • Hemangiopericytoma (9150)(Also known as "solitary fibrous tumor". Only a subset of these tumors are classified as malignant.)
    • Hemangiosarcoma (9120/3) (More commonly referred to as "angiosarcoma")
    • Kaposi's sarcoma (9140/3)
    • Leiomyosarcoma (8890/3-8896/3)
    • Liposarcoma (8850/3-8858/3)
    • Lymphangiosarcoma (9170-9175)
    • Lymphosarcoma (Not considered to be sarcomas)
    • Malignant fibrous histiocytoma (8830/3)(This is an obsolete term that is no longer recognized by the World Health Organization. Many of these tumors would currently be classified as "undifferentiated pleomorphic sarcoma".)
    • Malignant peripheral nerve sheath tumor (MPNST)
    • Neurofibrosarcoma (9540/3)
    • Rhabdomyosarcoma (8900-8920)
    • Synovial sarcoma (9040/3-9043/3)
    • Undifferentiated pleomorphic sarcoma (previously referred to as Malignant fibrous histiocytoma)


Surgery is important in the treatment of most sarcomas.[3] Limb sparing surgery, as opposed to amputation, can now be used to save the limbs of patients in at least 90% of extremity tumor cases.[3] Additional treatments, including chemotherapy and radiation therapy, may be administered before and/or after surgery.[1] Chemotherapy significantly improves the prognosis for many sarcoma patients, especially those with bone sarcomas.[4] Treatment can be a long and arduous process, lasting about a year for many patients.[1]

  • Liposarcoma treatment consists of surgical resection, with chemotherapy not being used outside of the investigative setting. Adjuvant radiotherapy may also be used after surgical excision for liposarcoma.[5]
  • Rhabdomyosarcoma is treated with surgery, radiotherapy, and/or chemotherapy.[6] The majority of rhabdomyosarcoma patients have between a 50–85% survival rate.[7]
  • Osteosarcoma is treated with surgical resection of as much of the cancer as possible, often along with neoadjuvant chemotherapy.[8] Radiotherapy is a second alternative although not as successful.


Sarcomas are quite rare with only 15,000 new cases per year in the United States.[9] Sarcomas therefore represent about one percent of the 1.5 million new cancer diagnoses in that country each year.[10]

Gastrointestinal stromal tumor (GIST) is the most common form of sarcoma, with approximately 3,000-3,500 cases per year in the United States.[11]

Sarcomas affect people of all ages. Approximately 50% of bone sarcomas and 20% of soft tissue sarcomas are diagnosed in people under the age of 35.[12] Some sarcomas, such as leiomyosarcoma, chondrosarcoma, and gastrointestinal stromal tumor (GIST), are more common in adults than in children. Most high-grade bone sarcomas, including Ewing's sarcoma and osteosarcoma, are much more common in children and young adults.


  1. 1.0 1.1 1.2 Buecker, P (2005). Sarcoma: A Diagnosis of Patience. ESUN 2 (5).
  2. Longhi A, Errani C, De Paolis M, Mercuri M, Bacci G (Oct 2006). Primary bone osteosarcoma in the pediatric age: state of the art. Cancer Treat Rev. 32 (6): 423–36.
  3. 3.0 3.1 Morris, C (2005). Malignant Fibrous Histiocytoma (MFH). ESUN 2 (2).
  4. Baker, L (2006). A Rose is a Rose or a Thorn is a Thorn. ESUN 3 (5).
  5. eMedicine article/1102007
  6. Rhabdomyosarcoma. Boston Children's Hospital.
  7. Wexler, L (2004). Rhabdomyosarcoma. ESUN 1 (4).
  8. eMedicine article/1256857
  9. Borden EC, Baker LH, Bell RS, et al. (Jun 2003). Soft tissue sarcomas of adults: state of the translational science. Clin Cancer Res. 9 (6): 1941–56.
  10. Cancer Facts & Figures 2009. American Cancer Society.
  11. Tran T, Davila JA, El-Serag HB (Jan 2005). The epidemiology of malignant gastrointestinal stromal tumors: an analysis of 1,458 cases from 1992 to 2000. Am J Gastroenterol 100 (1): 162–8.
  12. Darling, J (2007). A Different View of Sarcoma Statistics. ESUN 4 (6).

External links[]

Template:Soft tissue tumors and sarcomas

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