Skip to main content
Erschienen in: Virchows Archiv 6/2010

01.06.2010 | Case Report

Extensive biliary intraepithelial neoplasia (BilIN) and multifocal early intrahepatic cholangiocarcinoma in non-biliary cirrhosis

verfasst von: Anne-Laure Rougemont, Muriel Genevay, Thomas A. McKee, Magali Gremaud, Gilles Mentha, Laura Rubbia-Brandt

Erschienen in: Virchows Archiv | Ausgabe 6/2010

Einloggen, um Zugang zu erhalten

Abstract

Biliary intraepithelial neoplasia (BilIN), a preneoplastic condition that may precede invasive intrahepatic cholangiocarcinoma (ICC), has been compared to pancreatic intraepithelial neoplasia (PanIN), a precursor lesion of pancreatic carcinoma. Biliary tract carcinoma development and progression is associated with several gene alterations, but BilIN lesions have yet to be studied in detail by molecular techniques. We describe a case of extensive intrahepatic biliary dysplasia, with lesions ranging from BilIN-1 to BilIN-3 lesions, and multifocal microscopic ICC in hepatitis C virus (HCV)- and alcohol-related cirrhosis. The small ICC foci had remained undetected prior to transplantation. Fluorescence in situ hybridization (FISH) analysis was performed on three foci of BilIN-3 lesions and on three microinvasive ICC foci with a combination of three FISH probes directed against genes frequently altered in pancreatic and biliary tract carcinomas. FISH analysis revealed a CDKNA2 heterozygous deletion in one BilIN-3 focus, and in one non-contiguous ICC focus, although the deletion was just above the chosen threshold. No deletions were detected in the genomic regions encoding TP53 and SMAD4. This report documents for the first time the development of multifocal ICC in the setting of extensive biliary dysplasia in a patient with three risk factors, HCV infection, alcohol abuse, and cirrhosis, and suggests heterogeneous carcinogenesis in ICC and possible involvement of the CDKNA2 gene.
Literatur
1.
Zurück zum Zitat Wilentz RE, Iacobuzio-Donahue CA, Argani P et al (2000) Loss of expression of Dpc4 in pancreatic intraepithelial neoplasia: evidence that DPC4 inactivation occurs late in neoplastic progression. Cancer Res 60:2002–2006PubMed Wilentz RE, Iacobuzio-Donahue CA, Argani P et al (2000) Loss of expression of Dpc4 in pancreatic intraepithelial neoplasia: evidence that DPC4 inactivation occurs late in neoplastic progression. Cancer Res 60:2002–2006PubMed
2.
Zurück zum Zitat Zen Y, Adsay NV, Bardadin K et al (2007) Biliary intraepithelial neoplasia: an international interobserver agreement study and proposal for diagnostic criteria. Mod Pathol 20:701–709CrossRefPubMed Zen Y, Adsay NV, Bardadin K et al (2007) Biliary intraepithelial neoplasia: an international interobserver agreement study and proposal for diagnostic criteria. Mod Pathol 20:701–709CrossRefPubMed
3.
Zurück zum Zitat Zen Y, Sasaki M, Fujii T et al (2006) Different expression patterns of mucin core proteins and cytokeratins during intrahepatic cholangiocarcinogenesis from biliary intraepithelial neoplasia and intraductal papillary neoplasm of the bile duct—an immunohistochemical study of 110 cases of hepatolithiasi. J Hepatol 44:350–358CrossRefPubMed Zen Y, Sasaki M, Fujii T et al (2006) Different expression patterns of mucin core proteins and cytokeratins during intrahepatic cholangiocarcinogenesis from biliary intraepithelial neoplasia and intraductal papillary neoplasm of the bile duct—an immunohistochemical study of 110 cases of hepatolithiasi. J Hepatol 44:350–358CrossRefPubMed
4.
Zurück zum Zitat Itatsu K, Zen Y, Ohira S et al (2007) Immunohistochemical analysis of the progression of flat and papillary preneoplastic lesions in intrahepatic cholangiocarcinogenesis in hepatolithiasis. Liver Int 27:1174–1184PubMed Itatsu K, Zen Y, Ohira S et al (2007) Immunohistochemical analysis of the progression of flat and papillary preneoplastic lesions in intrahepatic cholangiocarcinogenesis in hepatolithiasis. Liver Int 27:1174–1184PubMed
5.
Zurück zum Zitat Nakanuma Y, Harada K, Ishikawa A et al (2003) Anatomic and molecular pathology of intrahepatic cholangiocarcinoma. J Hepatobiliary Pancreat Surg 10:265–281CrossRefPubMed Nakanuma Y, Harada K, Ishikawa A et al (2003) Anatomic and molecular pathology of intrahepatic cholangiocarcinoma. J Hepatobiliary Pancreat Surg 10:265–281CrossRefPubMed
6.
Zurück zum Zitat Shimonishi T, Sasaki M, Nakanuma Y (2000) Precancerous lesions of intrahepatic cholangiocarcinoma. J Hepatobiliary Pancreat Surg 7:542–550CrossRefPubMed Shimonishi T, Sasaki M, Nakanuma Y (2000) Precancerous lesions of intrahepatic cholangiocarcinoma. J Hepatobiliary Pancreat Surg 7:542–550CrossRefPubMed
7.
Zurück zum Zitat Bergquist A, Glaumann H, Stal P et al (2001) Biliary dysplasia, cell proliferation and nuclear DNA-fragmentation in primary sclerosing cholangitis with and without cholangiocarcinoma. J Intern Med 249:69–75CrossRefPubMed Bergquist A, Glaumann H, Stal P et al (2001) Biliary dysplasia, cell proliferation and nuclear DNA-fragmentation in primary sclerosing cholangitis with and without cholangiocarcinoma. J Intern Med 249:69–75CrossRefPubMed
8.
Zurück zum Zitat Ludwig J, Wahlstrom HE, Batts KP et al (1992) Papillary bile duct dysplasia in primary sclerosing cholangitis. Gastroenterology 102:2134–2138PubMed Ludwig J, Wahlstrom HE, Batts KP et al (1992) Papillary bile duct dysplasia in primary sclerosing cholangitis. Gastroenterology 102:2134–2138PubMed
9.
Zurück zum Zitat Martins EB, Fleming KA, Garrido MC et al (1994) Superficial thrombophlebitis, dysplasia, and cholangiocarcinoma in primary sclerosing cholangitis. Gastroenterology 107:537–542PubMed Martins EB, Fleming KA, Garrido MC et al (1994) Superficial thrombophlebitis, dysplasia, and cholangiocarcinoma in primary sclerosing cholangitis. Gastroenterology 107:537–542PubMed
10.
Zurück zum Zitat Fleming KA, Boberg KM, Glaumann H et al (2001) Biliary dysplasia as a marker of cholangiocarcinoma in primary sclerosing cholangitis. J Hepatol 34:360–365CrossRefPubMed Fleming KA, Boberg KM, Glaumann H et al (2001) Biliary dysplasia as a marker of cholangiocarcinoma in primary sclerosing cholangitis. J Hepatol 34:360–365CrossRefPubMed
11.
Zurück zum Zitat Kobayashi M, Ikeda K, Saitoh S et al (2000) Incidence of primary cholangiocellular carcinoma of the liver in Japanese patients with hepatitis C virus-related cirrhosis. Cancer 88:2471–2477CrossRefPubMed Kobayashi M, Ikeda K, Saitoh S et al (2000) Incidence of primary cholangiocellular carcinoma of the liver in Japanese patients with hepatitis C virus-related cirrhosis. Cancer 88:2471–2477CrossRefPubMed
12.
Zurück zum Zitat Torbenson M, Yeh MM, Abraham SC (2007) Bile duct dysplasia in the setting of chronic hepatitis C and alcohol cirrhosis. Am J Surg Pathol 31:1410–1413CrossRefPubMed Torbenson M, Yeh MM, Abraham SC (2007) Bile duct dysplasia in the setting of chronic hepatitis C and alcohol cirrhosis. Am J Surg Pathol 31:1410–1413CrossRefPubMed
13.
Zurück zum Zitat Aishima S, Nishihara Y, Tsujita E et al (2008) Biliary neoplasia with extensive intraductal spread associated with liver cirrhosis: a hitherto unreported variant of biliary intraepithelial neoplasia. Hum Pathol 39:939–947CrossRefPubMed Aishima S, Nishihara Y, Tsujita E et al (2008) Biliary neoplasia with extensive intraductal spread associated with liver cirrhosis: a hitherto unreported variant of biliary intraepithelial neoplasia. Hum Pathol 39:939–947CrossRefPubMed
14.
Zurück zum Zitat Perumal V, Wang J, Thuluvath P et al (2006) Hepatitis C and hepatitis B nucleic acids are present in intrahepatic cholangiocarcinomas from the United States. Hum Pathol 37:1211–1216CrossRefPubMed Perumal V, Wang J, Thuluvath P et al (2006) Hepatitis C and hepatitis B nucleic acids are present in intrahepatic cholangiocarcinomas from the United States. Hum Pathol 37:1211–1216CrossRefPubMed
15.
Zurück zum Zitat Uchida T, Shikata T, Tanaka E et al (1994) Immunoperoxidase staining of hepatitis C virus in formalin-fixed, paraffin-embedded needle liver biopsies. Virchows Arch 424:465–469CrossRefPubMed Uchida T, Shikata T, Tanaka E et al (1994) Immunoperoxidase staining of hepatitis C virus in formalin-fixed, paraffin-embedded needle liver biopsies. Virchows Arch 424:465–469CrossRefPubMed
16.
Zurück zum Zitat El-Serag HB, Engels EA, Landgren O et al (2009) Risk of hepatobiliary and pancreatic cancers after hepatitis C virus infection: a population-based study of U.S. veterans. Hepatology 49:116–123CrossRefPubMed El-Serag HB, Engels EA, Landgren O et al (2009) Risk of hepatobiliary and pancreatic cancers after hepatitis C virus infection: a population-based study of U.S. veterans. Hepatology 49:116–123CrossRefPubMed
17.
Zurück zum Zitat Rubbia-Brandt L, Brundler MA, Kerl K et al (1999) Primary hepatic diffuse large B-cell lymphoma in a patient with chronic hepatitis C. Am J Surg Pathol 23:1124–1130CrossRefPubMed Rubbia-Brandt L, Brundler MA, Kerl K et al (1999) Primary hepatic diffuse large B-cell lymphoma in a patient with chronic hepatitis C. Am J Surg Pathol 23:1124–1130CrossRefPubMed
18.
Zurück zum Zitat Aishima S, Kuroda Y, Nishihara Y et al (2007) Proposal of progression model for intrahepatic cholangiocarcinoma: clinicopathologic differences between hilar type and peripheral type. Am J Surg Pathol 31:1059–1067CrossRefPubMed Aishima S, Kuroda Y, Nishihara Y et al (2007) Proposal of progression model for intrahepatic cholangiocarcinoma: clinicopathologic differences between hilar type and peripheral type. Am J Surg Pathol 31:1059–1067CrossRefPubMed
19.
Zurück zum Zitat Genevay M, Dumonceau JM, Pache JC et al (2010) FISH as a tool to characterize genetic alterations in pancreatic adenocarcinoma. Pancreas (in press) Genevay M, Dumonceau JM, Pache JC et al (2010) FISH as a tool to characterize genetic alterations in pancreatic adenocarcinoma. Pancreas (in press)
20.
Zurück zum Zitat Mahlamaki EH, Barlund M, Tanner M et al (2002) Frequent amplification of 8q24, 11q, 17q, and 20q-specific genes in pancreatic cancer. Genes Chromosomes Cancer 35:353–358CrossRefPubMed Mahlamaki EH, Barlund M, Tanner M et al (2002) Frequent amplification of 8q24, 11q, 17q, and 20q-specific genes in pancreatic cancer. Genes Chromosomes Cancer 35:353–358CrossRefPubMed
21.
22.
Zurück zum Zitat Shiraishi K, Okita K, Harada T et al (2001) Comparative genomic hybridization analysis of genetic aberrations associated with development and progression of biliary tract carcinomas. Cancer 91:570–577CrossRefPubMed Shiraishi K, Okita K, Harada T et al (2001) Comparative genomic hybridization analysis of genetic aberrations associated with development and progression of biliary tract carcinomas. Cancer 91:570–577CrossRefPubMed
23.
Zurück zum Zitat Feldmann G, Beaty R, Hruban RH et al (2007) Molecular genetics of pancreatic intraepithelial neoplasia. J Hepatobiliary Pancreat Surg 14:224–232CrossRefPubMed Feldmann G, Beaty R, Hruban RH et al (2007) Molecular genetics of pancreatic intraepithelial neoplasia. J Hepatobiliary Pancreat Surg 14:224–232CrossRefPubMed
24.
Zurück zum Zitat Hruban RH, Goggins M, Parsons J et al (2000) Progression model for pancreatic cancer. Clin Cancer Res 6:2969–2972PubMed Hruban RH, Goggins M, Parsons J et al (2000) Progression model for pancreatic cancer. Clin Cancer Res 6:2969–2972PubMed
25.
Zurück zum Zitat Luttges J, Galehdari H, Brocker V et al (2001) Allelic loss is often the first hit in the biallelic inactivation of the p53 and DPC4 genes during pancreatic carcinogenesis. Am J Pathol 158:1677–1683PubMed Luttges J, Galehdari H, Brocker V et al (2001) Allelic loss is often the first hit in the biallelic inactivation of the p53 and DPC4 genes during pancreatic carcinogenesis. Am J Pathol 158:1677–1683PubMed
26.
Zurück zum Zitat Maitra A, Adsay NV, Argani P et al (2003) Multicomponent analysis of the pancreatic adenocarcinoma progression model using a pancreatic intraepithelial neoplasia tissue microarray. Mod Pathol 16:902–912CrossRefPubMed Maitra A, Adsay NV, Argani P et al (2003) Multicomponent analysis of the pancreatic adenocarcinoma progression model using a pancreatic intraepithelial neoplasia tissue microarray. Mod Pathol 16:902–912CrossRefPubMed
27.
Zurück zum Zitat Wilentz RE, Geradts J, Maynard R et al (1998) Inactivation of the p16 (INK4A) tumor-suppressor gene in pancreatic duct lesions: loss of intranuclear expression. Cancer Res 58:4740–4744PubMed Wilentz RE, Geradts J, Maynard R et al (1998) Inactivation of the p16 (INK4A) tumor-suppressor gene in pancreatic duct lesions: loss of intranuclear expression. Cancer Res 58:4740–4744PubMed
28.
Zurück zum Zitat Anonymous (1994) Intraobserver and interobserver variations in liver biopsy interpretation in patients with chronic hepatitis C. The French METAVIR Cooperative Study Group. Hepatology 20:15–20 Anonymous (1994) Intraobserver and interobserver variations in liver biopsy interpretation in patients with chronic hepatitis C. The French METAVIR Cooperative Study Group. Hepatology 20:15–20
29.
Zurück zum Zitat Caldas C, Hahn SA, da Costa LT et al (1994) Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinoma. Nat Genet 8:27–32CrossRefPubMed Caldas C, Hahn SA, da Costa LT et al (1994) Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinoma. Nat Genet 8:27–32CrossRefPubMed
30.
Zurück zum Zitat Hahn SA, Hoque AT, Moskaluk CA et al (1996) Homozygous deletion map at 18q21.1 in pancreatic cancer. Cancer Res 56:490–494PubMed Hahn SA, Hoque AT, Moskaluk CA et al (1996) Homozygous deletion map at 18q21.1 in pancreatic cancer. Cancer Res 56:490–494PubMed
31.
Zurück zum Zitat Hahn SA, Seymour AB, Hoque AT et al (1995) Allelotype of pancreatic adenocarcinoma using xenograft enrichment. Cancer Res 55:4670–4675PubMed Hahn SA, Seymour AB, Hoque AT et al (1995) Allelotype of pancreatic adenocarcinoma using xenograft enrichment. Cancer Res 55:4670–4675PubMed
32.
Zurück zum Zitat Redston MS, Caldas C, Seymour AB et al (1994) p53 mutations in pancreatic carcinoma and evidence of common involvement of homocopolymer tracts in DNA microdeletions. Cancer Res 54:3025–3033PubMed Redston MS, Caldas C, Seymour AB et al (1994) p53 mutations in pancreatic carcinoma and evidence of common involvement of homocopolymer tracts in DNA microdeletions. Cancer Res 54:3025–3033PubMed
33.
Zurück zum Zitat Rozenblum E, Schutte M, Goggins M et al (1997) Tumor-suppressive pathways in pancreatic carcinoma. Cancer Res 57:1731–1734PubMed Rozenblum E, Schutte M, Goggins M et al (1997) Tumor-suppressive pathways in pancreatic carcinoma. Cancer Res 57:1731–1734PubMed
34.
Zurück zum Zitat Ruas M, Peters G (1998) The p16INK4a/CDKN2A tumor suppressor and its relatives. Biochim Biophys Acta 1378:F115–F177PubMed Ruas M, Peters G (1998) The p16INK4a/CDKN2A tumor suppressor and its relatives. Biochim Biophys Acta 1378:F115–F177PubMed
35.
Zurück zum Zitat DeHaan RD, Kipp BR, Smyrk TC et al (2007) An assessment of chromosomal alterations detected by fluorescence in situ hybridization and p16 expression in sporadic and primary sclerosing cholangitis-associated cholangiocarcinomas. Hum Pathol 38:491–499CrossRefPubMed DeHaan RD, Kipp BR, Smyrk TC et al (2007) An assessment of chromosomal alterations detected by fluorescence in situ hybridization and p16 expression in sporadic and primary sclerosing cholangitis-associated cholangiocarcinomas. Hum Pathol 38:491–499CrossRefPubMed
36.
Zurück zum Zitat Sirivatanauksorn Y, Sirivatanauksorn V, Bhattacharya S et al (1999) Genomic heterogeneity in synchronous hepatocellular carcinomas. Gut 45:761–765PubMedCrossRef Sirivatanauksorn Y, Sirivatanauksorn V, Bhattacharya S et al (1999) Genomic heterogeneity in synchronous hepatocellular carcinomas. Gut 45:761–765PubMedCrossRef
37.
Zurück zum Zitat Nakanishi Y, Zen Y, Kondo S et al (2008) Expression of cell cycle-related molecules in biliary premalignant lesions: biliary intraepithelial neoplasia and biliary intraductal papillary neoplasm. Hum Pathol 39:1153–1161CrossRefPubMed Nakanishi Y, Zen Y, Kondo S et al (2008) Expression of cell cycle-related molecules in biliary premalignant lesions: biliary intraepithelial neoplasia and biliary intraductal papillary neoplasm. Hum Pathol 39:1153–1161CrossRefPubMed
38.
Zurück zum Zitat Soussi T, Beroud C (2001) Assessing TP53 status in human tumours to evaluate clinical outcome. Nat Rev Cancer 1:233–240CrossRefPubMed Soussi T, Beroud C (2001) Assessing TP53 status in human tumours to evaluate clinical outcome. Nat Rev Cancer 1:233–240CrossRefPubMed
39.
Zurück zum Zitat Kang YK, Kim WH, Lee HW et al (1999) Mutation of p53 and K-ras, and loss of sheterozygosity of APC in intrahepatic cholangiocarcinoma. Lab Invest 79:477–483PubMed Kang YK, Kim WH, Lee HW et al (1999) Mutation of p53 and K-ras, and loss of sheterozygosity of APC in intrahepatic cholangiocarcinoma. Lab Invest 79:477–483PubMed
Metadaten
Titel
Extensive biliary intraepithelial neoplasia (BilIN) and multifocal early intrahepatic cholangiocarcinoma in non-biliary cirrhosis
verfasst von
Anne-Laure Rougemont
Muriel Genevay
Thomas A. McKee
Magali Gremaud
Gilles Mentha
Laura Rubbia-Brandt
Publikationsdatum
01.06.2010
Verlag
Springer-Verlag
Erschienen in
Virchows Archiv / Ausgabe 6/2010
Print ISSN: 0945-6317
Elektronische ISSN: 1432-2307
DOI
https://doi.org/10.1007/s00428-010-0899-3

Weitere Artikel der Ausgabe 6/2010

Virchows Archiv 6/2010 Zur Ausgabe

Neu im Fachgebiet Pathologie

Molekularpathologische Untersuchungen im Wandel der Zeit

Open Access Biomarker Leitthema

Um auch an kleinen Gewebeproben zuverlässige und reproduzierbare Ergebnisse zu gewährleisten ist eine strenge Qualitätskontrolle in jedem Schritt des Arbeitsablaufs erforderlich. Eine nicht ordnungsgemäße Prüfung oder Behandlung des …

Vergleichende Pathologie in der onkologischen Forschung

Pathologie Leitthema

Die vergleichende experimentelle Pathologie („comparative experimental pathology“) ist ein Fachbereich an der Schnittstelle von Human- und Veterinärmedizin. Sie widmet sich der vergleichenden Erforschung von Gemeinsamkeiten und Unterschieden von …

Gastrointestinale Stromatumoren

Open Access GIST CME-Artikel

Gastrointestinale Stromatumoren (GIST) stellen seit über 20 Jahren ein Paradigma für die zielgerichtete Therapie mit Tyrosinkinaseinhibitoren dar. Eine elementare Voraussetzung für eine mögliche neoadjuvante oder adjuvante Behandlung bei …

Personalisierte Medizin in der Onkologie

Aufgrund des erheblichen technologischen Fortschritts in der molekularen und genetischen Diagnostik sowie zunehmender Erkenntnisse über die molekulare Pathogenese von Krankheiten hat in den letzten zwei Jahrzehnten ein grundlegender …