| Literature DB >> 28474162 |
T T Rau1, H Dawson2, A Hartmann3, J Rüschoff4.
Abstract
The pathologist can contribute to recognizing hereditary causes of colorectal cancer via morphology. By identifying so-called index patients, it is possible to take preventive measures in affected families. The precise definition of the clinical presentation and the histopathological phenotype help to narrow the spectrum of expected genetic alterations. Novelties within Lynch syndrome include the recognition of EPCAM as a fifth gene locus, as well as the newly defined Lynch-like syndrome with evidence of somatic mismatch repair (MMR) mutations. With regard to polyposis-associated syndromes, the spectrum of polyps, whether serrated, hamartomatous or classic adenoma, is of crucial importance. The resulting differential diagnosis includes (attenuated) familial adenomatous polyposis ([a]FAP), MUTYH-associated polyposis (MAP), polymerase proofreading-associated polyposis (PPAP), phosphatase and tensin homolog (PTEN) hamartoma tumor syndrome (PHTS), Peutz-Jeghers syndrome and juvenile polyposis, each with a specific genetic background.Entities:
Keywords: Juvenile polyposis; Lynch syndrome; Peutz-Jeghers syndrome; Phosphatase and tensin homolog (PTEN) hamartoma tumor syndrome (PHTS); Polymerase proofreading-associated polyposis (PPAP)
Mesh:
Year: 2017 PMID: 28474162 DOI: 10.1007/s00292-017-0294-9
Source DB: PubMed Journal: Pathologe ISSN: 0172-8113 Impact factor: 1.011