Background: Lynch syndrome (LS) is caused by germline mismatch repair (MMR) gene mutations. De novo MMR gene mutations are rare, and somatic mosaicism in LS is thought to be infrequent. We describe the first case of somatic mosaicism by a de novo MLH1 mutation for a patient diagnosed with a rectosigmoid adenocarcinoma at age 31. Methods: Twelve years after initial colorectal cancer diagnosis, tumor tissue of the patient was tested with sensitive next generation sequencing (NGS) analysis for the presence of somatic MMR mutations. Results: In tumor tissue, an inactivating MLH1 mutation (c.518_519del; p.(Tyr173Trpfs*18)) was detected, which was also present at low level in the blood of the patient. In both parents, as well as the patient's sisters, the mutation was not present. Conclusion: We show that low‐level mosaicism can be detected by using high‐coverage targeted NGS panels on constitutional and/or tumor DNA. This report illustrates that by using sensitive sequencing techniques, more cases of genetic diseases driven by mosaic mutations may be identified, with important clinical consequences for patients and family members.

Additional Metadata
Keywords Lynch syndrome, MLH1, mosaicism
Persistent URL dx.doi.org/10.1002/mgg3.699, hdl.handle.net/1765/118837
Journal Molecular Genetics & Genomic Medicine
Citation
Geurts-Giele, W.R., Rosenberg, E.H, van Rens, A, van Leerdam, M.E, Dinjens, W.N.M, & Bleeker, F.E. (2019). Somatic mosaicism by a de novo MLH1 mutation as a cause of Lynch syndrome. Molecular Genetics & Genomic Medicine, 7(7). doi:10.1002/mgg3.699