Rau T T, Dawson H, Hartmann A, Rüschoff J
Institut für Pathologie, Universität Bern, Murtenstrasse 31, 3008, Bern, Schweiz.
Pathologisches Institut, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Deutschland.
Pathologe. 2017 May;38(3):156-163. doi: 10.1007/s00292-017-0294-9.
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.
病理学家可以通过形态学来协助识别结直肠癌的遗传病因。通过识别所谓的索引患者,有可能在受影响的家庭中采取预防措施。对临床表现和组织病理学表型的精确界定有助于缩小预期基因改变的范围。林奇综合征的新进展包括将EPCAM识别为第五个基因位点,以及新定义的具有体细胞错配修复(MMR)突变证据的林奇样综合征。对于息肉病相关综合征,息肉的类型,无论是锯齿状、错构瘤性还是经典腺瘤性,都至关重要。由此产生的鉴别诊断包括(弱化型)家族性腺瘤性息肉病([a]FAP)、MUTYH相关息肉病(MAP)、聚合酶校对相关息肉病(PPAP)、磷酸酶和张力蛋白同源物(PTEN)错构瘤肿瘤综合征(PHTS)、黑斑息肉综合征和幼年性息肉病,每种都有特定的遗传背景。