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Morphometric and immunohistochemical study of cholangiolocellular carcinoma: comparison with non-neoplastic cholangiole, interlobular duct and septal duct
BACKGROUND/PURPOSE: The origin of cholangiolocellular carcinoma (CoCC) is still controversial. To solve this problem, morphometric and immunohistochemical features of CoCC were examined. MATERIALS AND METHODS: Cancerous ducts: 15 CoCC lesions from 13 resected and two autopsied cases. Non-neoplastic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Japan
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3311844/ https://www.ncbi.nlm.nih.gov/pubmed/22179577 http://dx.doi.org/10.1007/s00534-011-0483-5 |
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author | Maeno, Sawako Kondo, Fukuo Sano, Keiji Takada, Tadahiro Asano, Takehide |
author_facet | Maeno, Sawako Kondo, Fukuo Sano, Keiji Takada, Tadahiro Asano, Takehide |
author_sort | Maeno, Sawako |
collection | PubMed |
description | BACKGROUND/PURPOSE: The origin of cholangiolocellular carcinoma (CoCC) is still controversial. To solve this problem, morphometric and immunohistochemical features of CoCC were examined. MATERIALS AND METHODS: Cancerous ducts: 15 CoCC lesions from 13 resected and two autopsied cases. Non-neoplastic ducts: 20 specimens of non-cancerous areas of eight resected CoCC cases and of 12 resected hepatocellular carcinoma (HCC) cases. From these specimens, cholangioles, interlobular ducts of small size (ILD-S), interlobular ducts of medium size (ILD-M) and septal ducts were randomly selected. MORPHOMETRY: The outer and inner diameters of these ducts were measured. Immunohistochemistry: two hepatocyte markers [Hep Par 1 and α-fetoptotein (AFP)], two cholangiocyte markers (cytokeratin CK7, CK19), a marker for mucin (Muc1), a hepatic stem/progenitor cell marker (c-Kit) and epithelial membrane antigen (EMA) were used. RESULTS: Morphometry: both mean values of the outer and inner diameters of CoCC were far larger than those of cholangioles, and showed intermediate values between those of ILD-S and ILD-M. Immunohistochemistry: all ducts of CoCCs were negative for the two hepatocyte markers and positive for CK 7. Most CoCC ducts were positive for CK 19. Positive rate of c-Kit of cholangiole was most remote from that of CoCC. The positive rates of EMA in the membranous area of ducts were similarly very high in CoCC, cholangiole and ILD-S. CONCLUSION: These results suggest that CoCCs may originate from ILDs. |
format | Online Article Text |
id | pubmed-3311844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-33118442012-03-30 Morphometric and immunohistochemical study of cholangiolocellular carcinoma: comparison with non-neoplastic cholangiole, interlobular duct and septal duct Maeno, Sawako Kondo, Fukuo Sano, Keiji Takada, Tadahiro Asano, Takehide J Hepatobiliary Pancreat Sci Original Article BACKGROUND/PURPOSE: The origin of cholangiolocellular carcinoma (CoCC) is still controversial. To solve this problem, morphometric and immunohistochemical features of CoCC were examined. MATERIALS AND METHODS: Cancerous ducts: 15 CoCC lesions from 13 resected and two autopsied cases. Non-neoplastic ducts: 20 specimens of non-cancerous areas of eight resected CoCC cases and of 12 resected hepatocellular carcinoma (HCC) cases. From these specimens, cholangioles, interlobular ducts of small size (ILD-S), interlobular ducts of medium size (ILD-M) and septal ducts were randomly selected. MORPHOMETRY: The outer and inner diameters of these ducts were measured. Immunohistochemistry: two hepatocyte markers [Hep Par 1 and α-fetoptotein (AFP)], two cholangiocyte markers (cytokeratin CK7, CK19), a marker for mucin (Muc1), a hepatic stem/progenitor cell marker (c-Kit) and epithelial membrane antigen (EMA) were used. RESULTS: Morphometry: both mean values of the outer and inner diameters of CoCC were far larger than those of cholangioles, and showed intermediate values between those of ILD-S and ILD-M. Immunohistochemistry: all ducts of CoCCs were negative for the two hepatocyte markers and positive for CK 7. Most CoCC ducts were positive for CK 19. Positive rate of c-Kit of cholangiole was most remote from that of CoCC. The positive rates of EMA in the membranous area of ducts were similarly very high in CoCC, cholangiole and ILD-S. CONCLUSION: These results suggest that CoCCs may originate from ILDs. Springer Japan 2011-12-17 2012-05 /pmc/articles/PMC3311844/ /pubmed/22179577 http://dx.doi.org/10.1007/s00534-011-0483-5 Text en © Japanese Society of Hepato-Biliary-Pancreatic Surgery and Springer 2011 |
spellingShingle | Original Article Maeno, Sawako Kondo, Fukuo Sano, Keiji Takada, Tadahiro Asano, Takehide Morphometric and immunohistochemical study of cholangiolocellular carcinoma: comparison with non-neoplastic cholangiole, interlobular duct and septal duct |
title | Morphometric and immunohistochemical study of cholangiolocellular carcinoma: comparison with non-neoplastic cholangiole, interlobular duct and septal duct |
title_full | Morphometric and immunohistochemical study of cholangiolocellular carcinoma: comparison with non-neoplastic cholangiole, interlobular duct and septal duct |
title_fullStr | Morphometric and immunohistochemical study of cholangiolocellular carcinoma: comparison with non-neoplastic cholangiole, interlobular duct and septal duct |
title_full_unstemmed | Morphometric and immunohistochemical study of cholangiolocellular carcinoma: comparison with non-neoplastic cholangiole, interlobular duct and septal duct |
title_short | Morphometric and immunohistochemical study of cholangiolocellular carcinoma: comparison with non-neoplastic cholangiole, interlobular duct and septal duct |
title_sort | morphometric and immunohistochemical study of cholangiolocellular carcinoma: comparison with non-neoplastic cholangiole, interlobular duct and septal duct |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3311844/ https://www.ncbi.nlm.nih.gov/pubmed/22179577 http://dx.doi.org/10.1007/s00534-011-0483-5 |
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