Sarcoma is a rare type of cancer that develops in the connective tissue of the body which includes fat, blood vessels, nerves, bones, muscles, deep skin tissues, and cartilage. With more than 50 different subtypes of sarcomas, they are generally divided into two main groups: bone tumors and soft tissue tumors. Sarcomas are very rare and represent less than one percent of all cancers diagnosed in adults and children in the U.S. annually.

Evaluation and Diagnosis

Our team possesses the expertise to evaluate and treat both benign and malignant tumors in adults and children. Many tools are utilized to diagnosis both bone and soft tissue sarcomas including:


  • Physical examination
  • Blood tests, including checking the level of an enzyme called alkaline phosphatase.
  • X-rays can show the location, size, and shape of a tumor
  • Special imaging tests such as a bone scan, a CT (or CAT) scan, an MRI. Imaging studies help determine the size and location and extent of the tumor.
  • Biopsy of the bone or soft tissue tumor


We offer the most advanced options available for the treatment of rare tumors of the bone and soft tissue in both adult and pediatric patients. Many tumors or growths that develop in the bone and soft tissue are not cancerous and can be successfully treated by surgery alone. Some of these tumors will be diagnosed as cancers and need additional treatment provided by our expert multidisciplinary teams.

Examples of the types of tumors evaluated and treated by the Center:

Benign (Non-Cancerous) Tumors


  • Bone cysts
  • Chondroblastoma
  • Chondromyxoid fibroma
  • Enchondroma
  • Hemangioma
  • Histiocytosis
  • Osteoblastoma
  • Osteochondroma
  • Hemangioma
  • Osteoid osteoma


Our Adult Sarcoma Multidisciplinary Program has been treating patients with rare sarcoma tumors for more than a decade with tremendous success. A full range of state-of-the-art therapy options are available including the most recent and cutting-edge treatments involving novel chemotherapy and biologic agents as well as new treatment protocols endorsed by the National Cancer Institute. Our multidisciplinary approach to treatment includes a team comprised of a fellowship-trained orthopedic oncologist, musculoskeletal radiologist, musculoskeletal pathologist, as well as medical and radiation oncologists with expertise in treating rare sarcoma tumors.


In collaboration with the Herman and Walter Samuelson Children's Hospital at Sinai, our unique Pediatric Sarcoma Multidisciplinary Program provides highly specialized care for children and adolescents diagnosed with sarcoma tumors, which make up at least 15 percent of childhood cancers. Sinai Hospital is one of the only community-based hospital in the Country with a multidisciplinary team composed of a pediatric fellowship-trained orthopedic oncologist, pediatric medical oncologists, and radiation oncologists supported by a pediatric ICU to effectively treat malignant tumors in children. Our program specializes in limb sparing surgery for pediatric patients with primary malignant bone tumors such as Ewing's sarcoma and osteosarcoma.

Advacned Surgical and Treatment Options

Limb-Sparing Surgery As recently as 15 years ago, the surgical answer to an aggressive tumor of the extremity was amputation. While this may be necessary in certain cases, many patients can be successfully treated with limb sparing surgery, which is designed to save the limb while removing the tumor. We specialize in limb sparing surgery for patients with primary malignant bone tumors such as Ewing’s sarcoma and osteosarcoma. ‘Growing’ or expanding prostheses, bone grafts, and bone transplantation are all techniques used in these surgeries.


Clinical trials and Research. Discoveries made in scientific research laboratories translate into treatments available to patients through research studies or clinical trials. Our specialists ensures both our adult and pediatric patients have access to the most advanced treatment options available in a community-based hospital setting.