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  2. Liposarcoma - Wikipedia

    en.wikipedia.org/wiki/Liposarcoma

    For these localized forms of DDL, perioperative radiotherapy following National Comprehensive Cancer Network guidelines may also be considered. [8] Retroperitoneal DDL is the most common, surgically unaccessible and serious form of DDL: it has a recurrence rate of 66% and a five-year overall survival rate of 54%. [31]

  3. Soft-tissue sarcoma - Wikipedia

    en.wikipedia.org/wiki/Soft-tissue_sarcoma

    A soft-tissue sarcoma (STS) is a malignant tumor, a type of cancer, that develops in soft tissue. [1] A soft-tissue sarcoma is often a painless mass that grows slowly over months or years. They may be superficial or deep-seated. Any such unexplained mass must be diagnosed by biopsy. [2]

  4. Sarcoma - Wikipedia

    en.wikipedia.org/wiki/Sarcoma

    Considering that the total estimated number of new cancer diagnoses (all types of cancer) is 1,958,310, this means bone sarcomas represent only 0.2% of all new cancer diagnoses (making them the 30th most common type of cancer [26]) and soft-tissue sarcomas represent only 0.7% (making them the 22nd most common type of cancer [28]) of all new ...

  5. Angiosarcoma - Wikipedia

    en.wikipedia.org/wiki/Angiosarcoma

    Even with treatment, prognosis is poor, with a five-year survival rate of 30–38%. [1] [3] This is even worse in cardiac angiosarcoma and angiosarcoma of the liver, where prognosis may be as low as three months. [7] Angiosarcomas make up 1–2% of soft tissue sarcomas, which in turn make up less than 1% of adult cancer. [2]

  6. Rhabdomyosarcoma - Wikipedia

    en.wikipedia.org/wiki/Rhabdomyosarcoma

    Rhabdomyosarcoma is the most common soft-tissue sarcoma in children as well as the third most common solid tumor in children. Recent estimates place the incidence of the disease at approximately 4.5 case per 1 million children/adolescents with approximately 250 new cases in the United States each year.

  7. Alveolar rhabdomyosarcoma - Wikipedia

    en.wikipedia.org/wiki/Alveolar_rhabdomyosarcoma

    The four year survival rate without remission for local ARMS tumors is 65 percent, while the four year survival rate with metastatic ARMS is only 15 percent. [1] Patients who have metastatic ARMS positive with PAX3-FOXO1 fusion often have a poorer outcome than patients positive with PAX7-FOXO1 fusion, with a four-year survival rate of 8 percent ...

  8. Ewing sarcoma - Wikipedia

    en.wikipedia.org/wiki/Ewing_sarcoma

    Ewing sarcoma is a type of pediatric cancer [5] that forms in bone or soft tissue. [1] Symptoms may include swelling and pain at the site of the tumor, fever, and a bone fracture. [2] The most common areas where it begins are the legs, pelvis, and chest wall. [4]

  9. Epithelioid sarcoma - Wikipedia

    en.wikipedia.org/wiki/Epithelioid_sarcoma

    Epithelioid sarcoma is a slow-growing and relatively painless tumor, often resulting in a lengthy period of time between presentation and diagnosis. [8] Due to the difficulty of discerning this cancer as different from more common cancers, such as cancers of the skin (squamous cell carcinoma or basal cell carcinoma), it is often misdiagnosed, mistaken as a persistent wart or cyst.

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