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abstract
Glioblastomas, astrocytomas and oligodendrogliomas linked to Lynch syndrome
Background and purpose
Brain tumors represent a rare and relatively uncharacterized tumor type in Lynch syndrome.
Methods
The
national Danish Hereditary Nonpolyposis Colorectal Cancer Register was
utilized to estimate the cumulative life-time risk for brain tumors in
Lynch syndrome, and the mismatch repair (MMR) status in all tumors
available was evaluated.
Results
Primary
brain tumors developed in 41/288 families at a median age of 41.5
(range 2–73) years. Biallelic MMR gene mutations were linked to brain
tumor development in childhood. The risk of brain tumors was
significantly higher (2.5%) in MSH2 gene mutation carriers compared to patients with mutations in MLH1 or MSH6.
Glioblastomas predominated (56%), followed by astrocytomas (22%) and
oligodendrogliomas (9%). MMR status was assessed in 10 tumors, eight of
which showed MMR defects. None of these tumors showed
immunohistochemical staining suggestive of the IDH1 R132H mutation.
Conclusion
In Lynch syndrome brain tumors occurred in 14% of the families with significantly higher risks for individuals with MSH2 gene mutations and development of childhood brain tumors in individuals with constitutional MMR defects.
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