- Soft-tissue sarcoma
Soft-tissue sarcoma Classification and external resources ICD-9 171 DiseasesDB 31472 MeSH D018204
A soft-tissue sarcoma is a form of sarcoma that develops in connective tissue, though the term is sometimes applied to elements of the soft tissue that are not currently considered connective tissue.
Most soft-tissue sarcomas are not associated with any known risk factors or identifiable etiology. There are some exceptions:
- Studies suggest that workers who are exposed to chlorophenols in wood preservatives and phenoxy herbicides may have an increased risk of developing soft-tissue sarcomas. An unusual percentage of patients with a rare blood vessel tumor, angiosarcoma of the liver, have been exposed to vinyl chloride in their work. This substance is used in the manufacture of certain plastics, notably PVC.
- In the early 1900s, when scientists were just discovering the potential uses of radiation to treat disease, little was known about safe dosage levels and precise methods of delivery. At that time, radiation was used to treat a variety of noncancerous medical problems, including enlargement of the tonsils, adenoids, and thymus gland. Later, researchers found that high[vague] doses of radiation caused soft-tissue sarcomas in some patients. Because of this risk, radiation treatment for cancer is now planned to ensure that the maximum dosage of radiation is delivered to diseased tissue while surrounding healthy tissue is protected as much as possible.
- Kaposi's sarcoma, a rare cancer of the cells that line blood vessels in the skin and mucus membranes, is caused by Human herpesvirus 8. Kaposi's sarcoma often occurs in patients with AIDS (acquired immune deficiency syndrome). Kaposi's sarcoma, however, has different characteristics than typical soft-tissue sarcomas and is treated differently.
- In a very small fraction of cases, sarcoma may be related to a rare inherited genetic alteration of the p53 gene and is known as Li-Fraumeni syndrome. Certain other inherited diseases are associated with an increased risk of developing soft-tissue sarcomas. For example, people with neurofibromatosis type I (also called von Recklinghausen's disease, associated with alterations in the NF1 gene) are at an increased risk of developing soft-tissue sarcomas known as malignant peripheral nerve sheath tumors. Patients with inherited retinoblastoma have alterations in the RB1 gene, a tumor suppressor gene, and are likely to develop soft-tissue sarcomas as they mature into adulthood.
Soft-tissue sarcomas are relatively uncommon cancers. They account for less than 1% of all new cancer cases each year. This may be because cells in soft tissue, in contrast to tissues that more commonly give rise to malignancies, are not continuously dividing cells.
In 2006, about 9,500 new cases were diagnosed in the United States. Soft-tissue sarcomas are more commonly found in older patients (>50 years old) although in children and adolescents under age 20, certain histologies are common (rhabdomyosarcoma, synovial sarcoma).
In their early stages, soft-tissue sarcomas usually do not cause symptoms. Because soft tissue is relatively elastic, tumors can grow rather large, pushing aside normal tissue, before they are felt or cause any problems. The first noticeable symptom is usually a painless lump or swelling. As the tumor grows, it may cause other symptoms, such as pain or soreness, as it presses against nearby nerves and muscles. If in the abdomen it can cause abdominal pains commonly mistaken for menstrual cramps, indigestion, or cause constipation.
The only reliable way to determine whether a soft-tissue tumour is benign or malignant is through a biopsy. There are two methods for acquisition of tumour tissue for cytopathological analysis;
A pathologist examines the tissue under a microscope. If cancer is present, the pathologist can usually determine the type of cancer and its grade. Here, 'grade' refers to a scale used to represent concisely the predicted growth rate of the tumour and its tendency to spread, and this is determined by the degree to which the cancer cells appear abnormal when examined under a microscope. Low-grade sarcomas, although cancerous, are defined as those that are less likely to metastasise. High-grade sarcomas are defined as those more likely to spread to other parts of the body.
Soft tissue sarcomas commonly originate in the upper body, in the shoulder or upper chest. Some symptoms are uneven posture, pain in the trapezius muscle and cervical inflexibility [difficulty in turning the head].
The most common site to which soft tissue sarcoma spreads is the lungs.
In general, treatment for soft-tissue sarcomas depends on the stage of the cancer. The stage of the sarcoma is based on the size and grade of the tumor, and whether the cancer has spread to the lymph nodes or other parts of the body (metastasized). Treatment options for soft-tissue sarcomas include surgery, radiation therapy, and chemotherapy.
- Surgery is the most common treatment for soft-tissue sarcomas. If possible, the doctor will remove the cancer and a safe margin of the healthy tissue around it. It is important to obtain a margin free of tumor to decrease the likelihood of local recurrence and give the best chance for eradication of the tumor. Depending on the size and location of the sarcoma, it may, rarely, be necessary to remove all or part of an arm or leg.
- Radiation therapy may be used either before surgery to shrink tumors or after surgery to kill any cancer cells that may have been left behind. In some cases, it can be used to treat tumours that cannot be surgically removed. In multiple studies, radiation therapy has been found to improve the rate of local control, but has not had any influence on overall survival.
- Chemotherapy may be used with radiation therapy either before or after surgery to try to shrink the tumor or kill any remaining cancer cells. The use of chemotherapy to prevent the spread of soft-tissue sarcomas has not been proven to be effective. If the cancer has spread to other areas of the body, chemotherapy may be used to shrink tumors and reduce the pain and discomfort they cause, but is unlikely to eradicate the disease.
A combination of Taxotere and Gemzar could be an effective chemotherapy regimen in patients with advanced soft-tissue sarcoma.
Table 1: Major Types of Soft-Tissue Sarcomas in Adults Tissue of Origin Type of Cancer Usual Location in the Body Fibrous tissue Fibrosarcoma Arms, legs, trunk Malignant fibrous
Legs Dermatofibrosarcoma Trunk Fat Liposarcoma Arms, legs, trunk Muscle
- Striated muscle
- Smooth muscle
Arms, legs Uterus, digestive tract
Blood vessels Hemangiosarcoma Arms, legs, trunk Kaposi's sarcoma Legs, trunk Lymph vessels Lymphangiosarcoma Arms Synovial tissue
(linings of joint cavities, tendon sheaths)
Synovial sarcoma Legs Peripheral nerves Malignant peripheral nerve sheath tumour/Neurofibrosarcoma Arms, legs, trunk Cartilage and bone-forming tissue Extraskeletal chondrosarcoma Legs Extraskeletal osteosarcoma Legs, trunk (not involving the bone) Table 2: Major Types of Soft-Tissue Sarcomas in Children Tissue of Origin Type of Cancer Usual Location in the Body Most common ages Muscle
Head and neck, genitourinary tract Infant–4 Arms, legs, head, and neck Infant–19
Leiomyosarcoma Trunk 15–19 Fibrous tissue Fibrosarcoma Arms and legs 15–19 Malignant fibrous
Legs 15–19 Dermatofibrosarcoma Trunk 15–19 Fat Liposarcoma Arms and Legs 15–19 Blood vessels Infantile hemangio-
Arms, legs, trunk, head, and neck Infant–4 Synovial tissue
(linings of joint cavities, tendon sheaths)
Synovial sarcoma Legs, arms, and trunk 15–19 Peripheral nerves Malignant peripheral nerve sheath tumors (also called neurofibrosarcomas, malignant schwannomas, and neurogenic sarcomas) Arms, legs, and trunk 15–19 Muscular nerves Alveolar soft part sarcoma Arms and legs Infant–19 Cartilage and bone-forming tissue Extraskeletal myxoid chondrosarcoma Legs 10–14 Extraskeletal mesenchymal Legs 10–14
- Runner Terry Fox died from osteosarcoma.
- Actor Robert Urich died from synovial sarcoma.
- Actress Michelle Thomas died from desmoplastic small-round-cell tumor, a rare abdominal soft-tissue sarcoma.
- It Is Written evangelist Henry Fayenbrand died from sarcoma in his leg.
- Retired pathologist Professor Clair du Boulay OBE specialised in soft-tissue sarcomas at the University of Southampton.
- ^ "soft tissue sarcoma" at Dorland's Medical Dictionary
- ^ Ries LAG, Harkins D, Krapcho M, et al. SEER Cancer Statistics Review, 1975–2003. Bethesda , MD: National Cancer Institute, 2006.
- ^ http://professional.cancerconsultants.com/oncology_sarcoma_cancer_news.aspx?id=36670
- Factsheet from the National Cancer Institute
- Information from Memorial Sloan Kettering
- The Sarcoma Learning Center
- www.soft-tissue.com - a database of review questions on soft tissue sarcomas
- Clinically reviewed soft-tissue sarcoma information for patients, from Cancer Research UK.
Connective/soft tissue tumors and sarcomas (ICD-O 8800–9059) (C45–C49/D17–D21, 171/214–215) Not otherwise specified (8800–8809) Connective tissue neoplasmFibromatous (8810–8839)Fibroma/fibromatosis: Aggressive infantile fibromatosis · Aponeurotic fibroma · Collagenous fibroma · Diffuse infantile fibromatosis · Familial myxovascular fibromas · Fibroma of tendon sheath · Fibromatosis colli · Infantile digital fibromatosis · Juvenile hyaline fibromatosis · Plantar fibromatosis · Pleomorphic fibroma · Oral submucous fibrosisHistiocytoma/histiocytic sarcoma: Benign fibrous histiocytoma · Malignant fibrous histiocytoma · Atypical fibroxanthomaSolitary fibrous tumorMyxomatous (8840–8849)Fibroepithelial (9000–9039)Synovial-like (9040–9049) Lipomatous (8850–8889) Myomatous (8890–8929)skeletal muscle: Rhabdomyoma/rhabdomyosarcoma: Embryonal rhabdomyosarcoma (Sarcoma botryoides) · Alveolar rhabdomyosarcoma Complex mixed and stromal (8930–8999) Mesothelial (9050–9059)see also Template:Connective tissue
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Look at other dictionaries:
Soft tissue sarcoma — Infobox Disease Name = Soft tissue sarcoma Caption = DiseasesDB = 31472 ICD10 = ICD9 = ICD9|171 ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D018204 A soft tissue sarcoma is a rare form of cancer that develops in… … Wikipedia
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soft tissue sarcoma — A cancer that begins in the muscle, fat, fibrous tissue, blood vessels, or other supporting tissue of the body … English dictionary of cancer terms
Soft tissue sarcoma in cats and dogs — Soft tissue sarcoma refer to a broad group of tumors that originate from connective tissues. They tend to have similar histologic appearance and biological behavior, and can be either benign (noncancerous) or malignant (cancerous). Soft tissue… … Wikipedia
stage IA soft tissue sarcoma — Cancer in which the cells look very much like normal cells. The cancer is smaller than 5 centimeters (about 2 inches) and has not spread to lymph nodes or other parts of the body … English dictionary of cancer terms
stage IB soft tissue sarcoma — Cancer in which the cells look somewhat different from normal cells. The cancer is larger than 5 centimeters (about 2 inches) and has not spread to lymph nodes or other parts of the body … English dictionary of cancer terms
stage IIA soft tissue sarcoma — The cancer cells look somewhat different from normal cells. The cancer is larger than 5 centimeters (about 2 inches) and has not spread to lymph nodes or other parts of the body … English dictionary of cancer terms
stage IIB soft tissue sarcoma — The cancer cells look very different from normal cells. The cancer is smaller than 5 centimeters (about 2 inches) and has not spread to lymph nodes or other parts of the body … English dictionary of cancer terms
stage IIC soft tissue sarcoma — The cancer cells look very different from normal cells. The cancer is larger than 5 centimeters (about 2 inches) and has not spread to lymph nodes or other parts of the body … English dictionary of cancer terms