Osteosarcoma (also called osteogenic sarcoma) is the most common type of bone cancer and starts in the osteoblasts, which are the bone cells at the end of the long bones where new bone tissue forms as a young person grows.

Types of Osteosarcoma:

  • Periosteal Osteosarcoma
  • Parosteal sarcoma of bone
  • Telangiectatic Osteogenic Sarcoma
  • Small Cell Osteosarcoma

Osteosarcoma is most prevalent in teenagers, and most often forms in the bones near the knees of children and teenagers or in the bones surrounding the shoulder joints.

Causes of Osteosarcoma

Although a lot of research has been done into the causes of Osteosarcoma, nobody has been able to pinpoint the exact cause, as with most childhood cancers. There are, however, several risk factors that have been associated with Osteosarcoma, such as previous radiation therapy or anti-cancer drugs called alkylating agents.

Children carrying the hereditary retinoblastoma gene or who have other conditions such as Paget Disease, Werner Syndrome, Bloom Syndrome and Rothmund-Thomson syndrome may also be at risk.

Signs and Symptoms

Some of the typical signs and symptoms of Osteosarcoma are:

– Pain in the affected bone or joint that initially comes and goes but eventually becomes more severe, especially at night
– Swelling over a bone or bony part of the body
– A bone that breaks for no apparent reason or from a minor fall or accident

Tests and Diagnosis

Osteosarcoma can be diagnosed or staged using the following tests and procedures:

  • Physical Exam and History: The doctor will perform a physical examination, checking your child’s general health as well as checking for anything unusual or signs of cancer, and a complete medical history will be taken
  • MRI (Magnetic Resonance Imaging): An MRI or nuclear magnetic resonance imaging (NMRI), is a procedure whereby a series of detailed pictures is taken of the inside of the body using a computer, a magnet and radio waves
  • CT scan (CAT scan): This procedure may also be referred to as computed tomography, computerized tomography, or computerized axial tomography. A CAT scan takes a series of detailed pictures of the inside of the body from different angles, using a computer linked to an x-ray machine; a dye may also either be swallowed or injected into a vein to allow the organs and tissues to show up more clearly on the pictures.
  • A Biopsy: The type of biopsy that is done will depend on where the tumour is in the body as well as the size of the tumour:
    • Fine Needle Aspiration (FNA) Biopsy – removal of fluid or tissue using a thin needle
    • Core Biopsy – removal of tissue using a wide needle
    • Incisional Biopsy – a sample of tissue is removed through an incision in the skin
    • Excisional Biopsy – removal of an entire area of tissue or lump that looks abnormal

Other tests that may be done are x-rays, a complete blood count, blood chemistry studies, a bone scan,  or bone marrow aspiration.

Treatment Options

Treatment options consist of:

  • Chemotherapy: The use of a combination of anti-cancer drugs to destroy or shrink cancer cells is the preferred treatment for children, and may be done prior to and after surgery
  • Surgery: The tumour can often be removed by surgery done by a specialist orthopaedic surgeon. The type and extent of the surgery depends on the size and position of the tumour.
  • Limb-sparing Surgery: Most surgeons will perform limb-sparing surgery if at all possible. Limb-sparing surgery means that the bone is replaced by bone graft with bone taken from another part of the body or with a specially designed artificial part called a prosthesis
  • Amputation: In cases where it is not possible to just remove the cancerous portion of the affected bone, amputation of the limb may be necessary , after which a prosthesis (false limb) can be fitted
  • Radiotherapy: High-energy rays that destroy the cancer cells.

Some of the treatment options may result in after-effects such as nausea, vomiting, irritation or soreness of the skin from radiation, hair loss, risk of infection, fatigue, bruising and bleeding or diarrhoea. The doctor should explain all of this to you, but if they do not, please ask them about side effects.


At age 9, Jaliyah was diagnosed with an osteosarcoma. After swelling from an ankle sprain did not subside, a visit to Jaliyah’s primary care physician revealed that Jaliyah’s ankle pain was caused by a tumor. When local specialists recommended amputation, Jaliyah’s mother Joyce searched for second opinion to save her daughter’s leg. Joyce found Dr. Carol Morris, chief of Orthopaedic Oncology at The Johns Hopkins Hospital, who offered an alternative to amputation. Dr. Morris and her team performed a complex limb-sparing surgery allowing Jaliyah to keep her leg and giving her the chance to continue dancing.


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