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Precursor lesions of early onset pancreatic cancer

机译:早发性胰腺癌的前体病变

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Early onset pancreatic cancer (EOPC) constitutes less than 5% of all newly diagnosed cases of pancreatic cancer (PC). Although histopathological characteristics of EOPC have been described, no detailed reports on precursor lesions of EOPC are available. In the present study, we aimed to describe histopathological picture of extratumoral parenchyma in 23 cases of EOPCs (definition based on the threshold value of 45 years of age) with particular emphasis on two types of precursor lesions of PC: pancreatic intraepithelial neoplasia (PanIN) and intraductal papillary mucinous neoplasms (IPMNs). The types, grades, and densities of precursor lesions of PC were compared in patients with EOPCs, in young patients with neuroendocrine neoplasms (NENs), and in older (at the age of 46 or more) patients with PC. PanINs were found in 95.6% of cases of EOPCs. PanINs-3 were found in 39.1% of EOPC cases. Densities of all PanIN grades in EOPC cases were larger than in young patients with NENs. Density of PanINs-1A in EOPC cases was larger than in older patients with PC, but densities of PanINs of other grades were comparable. IPMN was found only in a single patient with EOPC but in 20% of older patients with PC. PanINs are the most prevalent precursor lesions of EOPC. IPMNs are rarely precursor lesions of EOPC. Relatively high density of low-grade PanINs-1 in extratumoral parenchyma of patients with EOPC may result from unknown multifocal genetic alterations in pancreatic tissue in patients with EOPCs.
机译:早发性胰腺癌(EOPC)占所有新诊断的胰腺癌(PC)病例的不到5%。尽管已经描述了EOPC的组织病理学特征,但是尚无关于EOPC前体病变的详细报道。在本研究中,我们旨在描述23例EOPCs(基于45岁阈值的定义)的肿瘤外实质的组织病理学图片,特别着重于PC的两种前体病变:胰腺上皮内瘤变(PanIN)和导管内乳头状黏液性肿瘤(IPMN)。比较了EOPCs患者,年轻的神经内分泌肿瘤(NENs)患者和年龄较大(≥46岁)的PC患者PC的前体病变的类型,等级和密度。在95.6%的EOPC中发现了PanIN。在39.1%的EOPC病例中发现了PanINs-3。在EOPC病例中,所有PanIN等级的密度均高于年轻的NEN患者。 EOPC病例中PanINs-1A的密度大于老年PC患者,但其他等级的PanINs-1A的密度却相当。 IPMN仅在一名EOPC患者中发现,但在20%的老年PC患者中发现。 PanIN是EOPC最普遍的前体病变。 IPMN很少是EOPC的前体病变。 EOPC患者肿瘤外实质中低级PanINs-1的相对较高密度可能是由于EOPC患者胰腺组织中未知的多灶基因改变所致。

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