Overview
- Large population-based studies have shown that a wide range of solid tumours occur significantly less frequently in children and adults with Down syndrome when compared with individuals without Down Syndrome.
- Some solid tumours seem to be more common; these include germ cell tumours, especially testicular tumours in boys/young men, and liver tumours.
- Treatment options need to be individualised regarding co-morbidities and communication difficulties.
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Prognosis is often as good or better in people with Down Syndrome with solid tumours.
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People with Down syndrome may be more susceptible to complications of chemotherapy.
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Cancer prevention strategies including advice on exercise and weight control will be appropriate, and as for the general population.
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Research into the reasons for the protective effect of Down syndrome in some cancers is ongoing.
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Haematological malignancies (AML and to a lesser extent ALL) are 10-20 times more common in individuals with Down syndrome, but are very rare over the age of 30 – see Blood Disorders topic page
- Prognosis may be worse in people with ALL and Down Syndrome.
Presentations at DSMIG Meetings
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Last reviewed: May 28th 2020 Dr Sarah Morris, Consultant Paediatrician