What is Neuroblastoma?
Neuroblastoma is a tumour arising from special (sympathetic)
nerve cells which run in a chain like fashion up the back of a
child's abdomen and chest and into the skull, following the line of
the spinal cord. The most common site for a neuroblastoma to grow
is in the abdomen. About 50% start in the adrenal gland lying above
the kidney but some tumours grow at the back of the chest and
occasionally even higher up towards the neck.
Signs & Symptoms
The site of the tumour may cause differing symptoms at the time
of diagnosis. For example, a tumour right at the back of the
abdomen, which has grown to press on the spinal cord, may, among
other possible symptoms, cause the child to begin to walk
unsteadily or to have difficulty passing urine. A child who has a
tumour in the chest may have problems with chest infections, cough
or fluid in the lung, and this may need treatment before the
neuroblastoma itself is treated. The child may also have loss of
appetite, vague aches and pains and sweating, or a lump may be felt
or seen.
Diagnosis
A specimen of urine is collected to test for catecholamine
levels. This substance, which is a hormone, is generally secreted
into the urine in raised levels when a child has Neuroblastoma.
Blood and urine tests, X-rays, a bone scan and bone marrow tests
will be performed. A CT or MRI scan or ultrasound will also be done
in order to show the extent or limit of the tumour. Usually, it is
necessary to take a biopsy of the tumour in order to confirm
diagnosis. (Refer to section on tests and procedures)
Treatment
The extent or spread of the tumour will determine what
chemotherapy will be required. Surgery can be difficult as is not
usually done until the tumour has been shrunk by chemotherapy to a
more manageable size.
Follow up care
After treatment has finished the child will be seen at regular
intervals. Clinical examinations, urine, blood and ultrasound scans
to monitor progress will be carried out to detect any possible
recurrence After the first few years the focus of follow up changes
to monitoring growth and development and other possible later side
effects of treatment.