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Childhood Cancers: Wilms' Tumour
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Description
Wilms' tumour or nephroblastoma
is a cancer of the kidneys that can develop in a foetus but may not cause
symptoms for years after birth. Wilms' tumour usually occurs in children
under 5 years of age, although it appears occasionally in older children
and rarely in adults. The cause of Wilms' tumour isn't known, although
a genetic abnormality may be involved. Children with certain , such as absence of the irises (eye structure) or excessive
growth of one side of the body, both of which may be caused by a genetic
abnormality, have an increased risk of developing Wilms' tumour.
Symptoms and Signs
Symptoms include a large abdomen (for example, a rapid change
to a larger diaper size), abdominal pain, fever, poor appetite, nausea,
and vomiting. Blood appears in the urine in 15 to 20% of cases. Wilms'
tumour may cause high blood pressure. This cancer can spread to other
parts of the body, especially the lungs, producing a cough and shortness
of breath.
Diagnosis and Treatment
If a child has symptoms, the doctor will usually feel
the child's abdomen for lumps and run blood and urine tests. If Wilms'
tumour is suspected, an ,
a (CT) scan,
or a
(MRI) scan may be performed to determine the nature and size of the lump.
A special x-ray called an intravenous pyelogram ,
which uses a dye containing iodine in order to see the kidney more clearly.
The prognosis depends on the microscopic appearance of the tumour, its
spread at the time of diagnosis, and the age of the child. Younger children,
children with smaller tumours, and children whose tumour has not spread
tend to fare better. Wilms' tumour is curable in the majority of affected
children. Surgery, chemotherapy
and radiation
therapy are the options available to treat this form of cancer.
The information in this page is presented in summarised form and has been taken
from the following source(s):
1.
Pediatric Cancers, University of Pennsylvania Cancer Center: http://cancer.med.upenn.edu/
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