NIH Record - National Institutes of Health

Benign Nail Condition Linked to Rare Syndrome that Increases Cancer Risk

The presence of a benign nail abnormality may lead to the diagnosis of a rare inherited disorder that increases the risk of developing cancerous tumors of the skin, eyes, kidneys and the tissue that lines the chest and abdomen (e.g., the mesothelium). The condition, known as BAP1 tumor predisposition syndrome, is caused by mutations in the BAP1 gene, which normally acts as a tumor suppressor, among other functions. The findings are published in JAMA Dermatology.

Hassan, in a white lab coat, poses against a multicolored background.
Dr. Raffit Hassan

Scientists happened upon the discovery while studying participants who were enrolled in a screening for BAP 1 variants at the NIH Clinical Center. As part of the study, a dermatology screening was performed at enrollment and annually for participants aged 2 and older.

Patients were asked about nail health during a baseline genetic assessment, and one reported noticing subtle changes in his nails. His observation prompted investigators to evaluate other participants for nail changes and uncover this new finding.

Biopsies of the nail and underlying nail bed in several participants confirmed the investigators’ suspicion of a benign tumor abnormality known as an onychopapilloma. The condition causes a colored band (usually white or red) along the length of the nail, along with thickening of the nail underlying the color change and thickening at the end of the nail. It typically only affects one nail.

However, among study participants with known BAP1 tumor predisposition syndrome aged 30 and older, 88% had onychopapilloma tumors affecting multiple nails. Researchers suggest that nail screening may be particularly valuable in a patient with a personal or family history of melanoma or other potential BAP1-associated malignancy.

Dr. Raffit Hassan, principal investigator of the clinical protocol in which these patients were enrolled, said, “This discovery is an excellent example of how multidisciplinary teams and natural history studies can reveal insights about rare diseases.”

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Editor: Dana Talesnik
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Associate Editor: Patrick Smith
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Staff Writer: Amber Snyder
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