Nobukawa Bunsei, Suda Koichi, Yamasaki Shigetaka, Takase Masaru, Fukumura Yuki, Shiono Saori
Department of Pathology (I), Juntendo University School of Medicine, Tokyo, Japan.
Nihon Geka Gakkai Zasshi. 2003 Jun;104(6):439-42.
Many intraductal papillary-mucinous tumors (IPMTs) have been diagnosed with improvements in diagnostic imaging techniques. The histology of IPMT is various, including hyperplasia to invasive carcinoma. IPMTs are thought to occur multicentrically through the hyperplasia-adenoma-carcinoma sequence. IPMTs are characterized by genetic heterogeneity associated with histologic heterogeneity that may be due to slow growth and favorable prognosis. However, some IPMTs progress to invasive pancreatic cancer through malignant transformation with aggressive clonal progression. Thus some conventional pancreatic cancers may be derived from IPMTs. Although IPMTs and conventional pancreatic cancer initially occur in the ductal epithelium, they are thought to be totally different entities in terms of large or peripheral pancreatic duct origin, developmental style, genetic alterations, and prognosis. In future, differences and/or similarities will be discussed on the basis of molecular analyses of the carcinogensis of both tumors.
随着诊断成像技术的进步,许多导管内乳头状黏液性肿瘤(IPMTs)得以确诊。IPMT的组织学表现多样,包括从增生到浸润性癌。IPMTs被认为是通过增生-腺瘤-癌序列多中心发生的。IPMTs的特征是与组织学异质性相关的基因异质性,这可能归因于其生长缓慢和预后良好。然而,一些IPMTs通过恶性转化和侵袭性克隆进展发展为侵袭性胰腺癌。因此,一些传统的胰腺癌可能起源于IPMTs。尽管IPMTs和传统胰腺癌最初都发生于导管上皮,但就胰腺大导管或周边导管起源、发育方式、基因改变和预后而言,它们被认为是完全不同的实体。未来,将基于对这两种肿瘤发生机制的分子分析来探讨它们的差异和/或相似之处。