The Evening Leader

To Your Good Health

- Dr. Keith Roach, M.D.

DEAR DR. ROACH: My cousin was in his mid-40s when he died of a brain tumor, over 10 years ago. After having similar symptoms, my other cousin, his older sister, who is in her mid-60s, just had surgery to remove a cancerous brain tumor. Is it possible this could be hereditary? Neither of them had any kids, but they have an older brother. Should he get tested? Is this even something you can get tested for? — J.A.M.

ANSWER: Many cancers run in families, some more so than others. Primary brain cancers are uncommon, and there are different types. A primary brain cancer is one that starts in the brain, as opposed to when cancer in a different area of the body spreads to the brain, which is much more common. Many cancers that can metastasiz­e to the brain run in families.

Two of the more common types of primary brain cancers are astrocytom­as and glioblasto­mas. A recent review found that there is a familial component to astrocytom­as but not to glioblasto­mas. People with a family history of astrocytom­as are four times more likely to develop one; however, it would still be unusual to develop a brain cancer even with a family history.

The biggest risk for brain cancer is ionizing radiation, such as a person would get from radiation treatment of a childhood cancer. However, back in the 1950s, radiation was used to treat skin infections on the head, which has led to an increased risk of brain cancer in those so treated. Your cousins are not old enough for this kind of exposure, however.

There are some unusual genetic conditions that increase risk for brain tumors, including neurofibro­matosis type 2 and multiple endocrine neoplasia type 1.

Since the likelihood of developing a brain tumor is small, even with the family history, I don’t think I would advise screening for their brother. I did look for any studies that might be ongoing to test whether there might be a benefit to screening; unfortunat­ely, I did not find any at ClinicalTr­ials.gov.

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