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Neuroblastoma is a rare cancer that affects children. It develops from nerve cells called neuroblasts.
The cancer usually starts in the child’s abdomen (tummy). It often develops in the adrenal glands, the two small glands above the kidneys, and can spread to other areas such as the bones, liver and skin.
The cause is unknown. There are rare cases where children in the same family are affected, but it does not generally run in families.
Neuroblastoma affects around 100 children each year in the UK. It usually affects children under the age of five, and can occur before a child is born. It is the most common solid tumour in childhood after brain tumours.
The symptoms depend on where the cancer is and whether it has spread. It is often hard to diagnose neuroblastoma in the early stages, as initial symptoms are common ones – for example, aches and pains and loss of appetite.
However, the most common symptom when the cancer has developed is a lump or swelling in the child’s abdomen, as this is where the cancer usually starts. It can cause constipation and general discomfort and pain.
Other possible symptoms are:
Because early symptoms are vague, neuroblastoma is often not diagnosed until it has spread around the body (Stage 4).
The outlook is generally better if the child is younger and the cancer is low risk (growing slowly) and at a low stage.
Babies with Stage 4s neuroblastoma who have no symptoms may not need treatment, as the cancer may go away on its own.
With all other stages of neuroblastoma, the tumour is removed by operation. Depending on the stage, chemotherapy and/or radiotherapy is sometimes used before surgery to shrink the tumour and after surgery to kill any remaining cancer cells.
It is common for the cancer to return after being treated.
Important: Our website provides useful information but is not a substitute for medical advice. You should always seek the advice of your doctor when making decisions about your health.