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Meet the VICC Ambassadors

Learn why we have joined VICC Ambassadors and how you can help us achieve Victory Over Cancer. 

Who We Are

Vanderbilt-Ingram Cancer Center is a leader in the prevention, diagnosis and treatment of cancer. The center's world-renowned team of experts provides an integrated, personalized and patient-centered approach to cancer care, including treatment, research, support, education and outreach. From a wide variety of wellness programs to a leading REACH for Survivorship Clinic, patients find support from diagnosis through survivorship.

Cancers A-Z

Cancer Information Summaries from the National Cancer Institute's Physician Data Query (PDQ®) provide prognostic and treatment information for major types of adult and pediatric cancers. 

Additionally, an overview of Cancer Information Summaries related to Genetics are also available: Genetics Summary

Meet the Research Advocates

Research advocates at Vanderbilt-Ingram Cancer Center support our research efforts in many ways and for many reasons. Our advocates are cancer survivors, caregivers, and community members who are committed to making a difference. 

Careers at Vanderbilt-Ingram Cancer Center

Vanderbilt-Ingram Cancer Center is a leader in the prevention, diagnosis and treatment of cancer. The center's world-renowned team of experts provides an integrated, personalized and patient-centered approach to cancer care, including treatment, research, support, education and outreach. From a wide variety of wellness programs to a leading REACH for Survivorship Clinic, patients find support from diagnosis through survivorship.

Wilms Tumor and Other Childhood Kidney Tumors
  • Childhood kidney tumors are diseases in which malignant (cancer) cells form in the tissues of the kidney.
  • There are many types of childhood kidney tumors.
    • Wilms Tumor
    • Renal Cell Cancer (RCC)
    • Rhabdoid Tumor of the Kidney
    • Clear Cell Sarcoma of the Kidney
    • Congenital Mesoblastic Nephroma
    • Ewing Sarcoma of the Kidney
    • Primary Renal Myoepithelial Carcinoma
    • Cystic Partially Differentiated Nephroblastoma
    • Multilocular Cystic Nephroma
    • Primary Renal Synovial Sarcoma
    • Anaplastic Sarcoma of the Kidney
  • Nephroblastomatosis is not cancer but may become Wilms tumor.
  • Having certain genetic syndromes, other conditions, or environmental exposures can increase the risk of Wilms tumor.
  • Tests are used to screen for Wilms tumor.
  • Having certain conditions may increase the risk of renal cell cancer.
  • Treatment for Wilms tumor and other childhood kidney tumors may include genetic counseling.
  • Signs of Wilms tumor and other childhood kidney tumors include a lump in the abdomen and blood in the urine.
  • Tests that examine the kidney and the blood are used to diagnose Wilms tumor and other childhood kidney tumors.
  • Certain factors affect prognosis (chance of recovery) and treatment options.
Soft Tissue Sarcoma
  • Childhood soft tissue sarcoma is a disease in which malignant (cancer) cells form in soft tissues of the body.
  • Soft tissue sarcoma occurs in children and adults.
  • Having certain diseases and inherited disorders can increase the risk of childhood soft tissue sarcoma.
  • The most common sign of childhood soft tissue sarcoma is a painless lump or swelling in soft tissues of the body.
  • Diagnostic tests are used to diagnose childhood soft tissue sarcoma.
  • If tests show there may be a soft tissue sarcoma, a biopsy is done.
  • There are many different types of soft tissue sarcomas.
    • Fat tissue tumors
    • Bone and cartilage tumors
    • Fibrous (connective) tissue tumors
    • Skeletal muscle tumors
    • Smooth muscle tumors
    • So-called fibrohistiocytic tumors
    • Nerve sheath tumors
    • Pericytic (Perivascular) Tumors
    • Tumors of unknown cell origin
    • Blood vessel tumors
  • Certain factors affect prognosis (chance of recovery) and treatment options.
Rhabdomyosarcoma
  • Childhood rhabdomyosarcoma is a disease in which malignant (cancer) cells form in muscle tissue.
  • Certain genetic conditions increase the risk of childhood rhabdomyosarcoma.
  • A sign of childhood rhabdomyosarcoma is a lump or swelling that keeps getting bigger.
  • Diagnostic tests and a biopsy are used to diagnose childhood rhabdomyosarcoma.
  • Certain factors affect prognosis (chance of recovery) and treatment options.
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