| Literature DB >> 25031730 |
Yasuni Nakanuma1, Yasunori Sato2, Hidenori Ojima3, Yae Kanai3, Shinichi Aishima4, Masakazu Yamamoto5, Shun-ichi Ariizumi5, Toru Furukawa6, Hiroki Hayashi7, Michiaki Unno7, Tetsuo Ohta8.
Abstract
Cholangiocarcinoma (CC) of the biliary tract occasionally presents a predominant intraductal papillary growth in the bile ducts, called as biliary tract carcinoma (BTC) of papillary growth (PG) and intrahepatic CC (ICC) of intraductal growth (IG) type. Recently, intraductal papillary neoplasm of bile duct (IPNB) has been proposed as a pre-invasive biliary neoplasm. This study was performed to characterize pathologically BTC of PG type and ICC of IG type with respect to IPNB. It was found that 126 of such 154 CCs (81.8%) fulfilled the criteria of IPNB, while the remaining 28 cases showed different histologies, such as tubular adenocarcinoma and carcinosarcoma. These IPNBs occurred in old aged patients with a male predominance, and the left lobe was rather frequently affected in the liver. A majority of these cases were high grade IPNB (43 cases) and invasive IPNB (77 cases), while low grade IPNB was rare (6 cases). Pancreatobiliary type was predominant (48 cases) followed by gastric (30 cases), intestinal (29 cases) and oncocytic (19 cases) types. Mucus hypersecretion was found in 45 cases, and this was frequent in IPNB at the intrahepatic large bile duct and hilar bile ducts but rare at the extrahepatic bile ducts. Interestingly, 36 cases of high grade and invasive IPNBs contained foci of moderately differentiated adenocacinoma within the intraductal papillary tumor. In conclusion, a majority of ICC of IG type and BTC of PG type could be regarded as a IPNB lineage, and clinically detectable IPNBs were already a malignant papillary lesion.Entities:
Keywords: Biliary tree; intraductal cholangiocarcinoma; intraductal papillary neoplasm; papillary cholangiocarcinoma; phenotype
Mesh:
Year: 2014 PMID: 25031730 PMCID: PMC4097227
Source DB: PubMed Journal: Int J Clin Exp Pathol ISSN: 1936-2625