4.4 Article

Cafe-au-lait macules and pediatric malignancy caused by biallelic mutations in the DNA mismatch repair (MMR) gene PMS2

Journal

PEDIATRIC BLOOD & CANCER
Volume 50, Issue 6, Pages 1268-1270

Publisher

WILEY
DOI: 10.1002/pbc.21514

Keywords

cafe-au-lait macules; inherited cancer syndrome; mismatch repair genes; neurofibromatosis type1; PMS2

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A 14-year-old male presented with a T4 sigmoid adenocarcinoma, <10 colonic adenomas and multiple cafe-au-lait rnacules. Family history was not suggestive of a dominant hereditary form of colorectal cancer. Evaluation of the tumor revealed abnormal immunohistochemical staining of the PMS2 protein and high frequency microsatellite instability. Germline analysis identified biallelic PMS2 missense mutations. A new cancer syndrome caused by biallelic mutations in the mismatch repair genes, including PMS2, is now emerging and is characterized by cafe-au-lait macules, colonic polyps and a distinctive tumor spectrum.

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