Cholangiocarcinoma arising in von Meyenburg complexes: Report of four cases
Although von Meyenburg complexes (VMC) are largely considered to be innocuous, neoplastic transformations have been described. The present report describes four cases of cholangiocarcinoma (CC) occurring on a background of VMC. The patients were all male and aged 69, 59, 68 and 75 years, respectivel...
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description | Although von Meyenburg complexes (VMC) are largely considered to be innocuous, neoplastic transformations have been described. The present report describes four cases of cholangiocarcinoma (CC) occurring on a background of VMC. The patients were all male and aged 69, 59, 68 and 75 years, respectively. While two patients were asymptomatic, the other two had a history of colon cancer. Radiologically the tumors measured 3, 4, 4.5 and 10 cm and were well enhanced from the arterial to delayed portal phase. Microscopically, the tumor consisted of multiple foci of characteristic VMC, and had a gradual transition from VMC to hyperplasia or dysplasia and well‐ to moderately differentiated adenocarcinomas. One patient had combined hepatocellular carcinoma (HCC) and CC, occurring in the high grade dysplastic nodule and VMC. On immunohistochemistry the epithelial cells of the VMC and CC were immunopositive for cytokeratin (CK) 7 in three patients, with another patient being focally positive only for CK19. The Ki‐67 labeling indices increased from the VMC to the dysplastic areas and then to the carcinomas. As a potentially precancerous lesion, VMC should be carefully followed up in terms of any size increases. Thus, biopsies are essential to determine any proliferative epithelial changes including dysplasia and malignant transformation. |
doi_str_mv | 10.1111/j.1440-1827.2008.02264.x |
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The present report describes four cases of cholangiocarcinoma (CC) occurring on a background of VMC. The patients were all male and aged 69, 59, 68 and 75 years, respectively. While two patients were asymptomatic, the other two had a history of colon cancer. Radiologically the tumors measured 3, 4, 4.5 and 10 cm and were well enhanced from the arterial to delayed portal phase. Microscopically, the tumor consisted of multiple foci of characteristic VMC, and had a gradual transition from VMC to hyperplasia or dysplasia and well‐ to moderately differentiated adenocarcinomas. One patient had combined hepatocellular carcinoma (HCC) and CC, occurring in the high grade dysplastic nodule and VMC. On immunohistochemistry the epithelial cells of the VMC and CC were immunopositive for cytokeratin (CK) 7 in three patients, with another patient being focally positive only for CK19. The Ki‐67 labeling indices increased from the VMC to the dysplastic areas and then to the carcinomas. As a potentially precancerous lesion, VMC should be carefully followed up in terms of any size increases. Thus, biopsies are essential to determine any proliferative epithelial changes including dysplasia and malignant transformation.</description><identifier>ISSN: 1320-5463</identifier><identifier>EISSN: 1440-1827</identifier><identifier>DOI: 10.1111/j.1440-1827.2008.02264.x</identifier><identifier>PMID: 18705771</identifier><language>eng</language><publisher>Melbourne, Australia: Blackwell Publishing Asia</publisher><subject>Aged ; Bile Duct Neoplasms - complications ; Bile Duct Neoplasms - pathology ; Bile Duct Neoplasms - surgery ; Bile Ducts, Intrahepatic - pathology ; Carcinoma, Hepatocellular - pathology ; Cell Transformation, Neoplastic ; cholangiocarcinoma ; Cholangiocarcinoma - complications ; Cholangiocarcinoma - pathology ; Cholangiocarcinoma - surgery ; cytokeratin 7 ; Disease-Free Survival ; Fatal Outcome ; Hamartoma - complications ; Hamartoma - pathology ; Humans ; Immunohistochemistry ; Ki‐67 antigen ; Liver Diseases - complications ; Liver Diseases - pathology ; Liver Neoplasms - pathology ; Male ; Middle Aged ; Precancerous Conditions - pathology ; Tomography, X-Ray Computed ; von Meyenburg complex</subject><ispartof>Pathology international, 2008-08, Vol.58 (8), p.503-512</ispartof><rights>2008 The Authors. Journal compilation © 2008 Japanese Society of Pathology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4864-e6c493236ae56683ffe7bf4e8eb6d6fa7c5b0fd73e92c2c79fcb825c82a2ec8c3</citedby><cites>FETCH-LOGICAL-c4864-e6c493236ae56683ffe7bf4e8eb6d6fa7c5b0fd73e92c2c79fcb825c82a2ec8c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1440-1827.2008.02264.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1440-1827.2008.02264.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18705771$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Song, Joon Seon</creatorcontrib><creatorcontrib>Lee, Young‐Joo</creatorcontrib><creatorcontrib>Kim, Kyoung Won</creatorcontrib><creatorcontrib>Huh, Jooryung</creatorcontrib><creatorcontrib>Jang, Se Jin</creatorcontrib><creatorcontrib>Yu, Eunsil</creatorcontrib><title>Cholangiocarcinoma arising in von Meyenburg complexes: Report of four cases</title><title>Pathology international</title><addtitle>Pathol Int</addtitle><description>Although von Meyenburg complexes (VMC) are largely considered to be innocuous, neoplastic transformations have been described. The present report describes four cases of cholangiocarcinoma (CC) occurring on a background of VMC. The patients were all male and aged 69, 59, 68 and 75 years, respectively. While two patients were asymptomatic, the other two had a history of colon cancer. Radiologically the tumors measured 3, 4, 4.5 and 10 cm and were well enhanced from the arterial to delayed portal phase. Microscopically, the tumor consisted of multiple foci of characteristic VMC, and had a gradual transition from VMC to hyperplasia or dysplasia and well‐ to moderately differentiated adenocarcinomas. One patient had combined hepatocellular carcinoma (HCC) and CC, occurring in the high grade dysplastic nodule and VMC. On immunohistochemistry the epithelial cells of the VMC and CC were immunopositive for cytokeratin (CK) 7 in three patients, with another patient being focally positive only for CK19. The Ki‐67 labeling indices increased from the VMC to the dysplastic areas and then to the carcinomas. As a potentially precancerous lesion, VMC should be carefully followed up in terms of any size increases. Thus, biopsies are essential to determine any proliferative epithelial changes including dysplasia and malignant transformation.</description><subject>Aged</subject><subject>Bile Duct Neoplasms - complications</subject><subject>Bile Duct Neoplasms - pathology</subject><subject>Bile Duct Neoplasms - surgery</subject><subject>Bile Ducts, Intrahepatic - pathology</subject><subject>Carcinoma, Hepatocellular - pathology</subject><subject>Cell Transformation, Neoplastic</subject><subject>cholangiocarcinoma</subject><subject>Cholangiocarcinoma - complications</subject><subject>Cholangiocarcinoma - pathology</subject><subject>Cholangiocarcinoma - surgery</subject><subject>cytokeratin 7</subject><subject>Disease-Free Survival</subject><subject>Fatal Outcome</subject><subject>Hamartoma - complications</subject><subject>Hamartoma - pathology</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Ki‐67 antigen</subject><subject>Liver Diseases - complications</subject><subject>Liver Diseases - pathology</subject><subject>Liver Neoplasms - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Precancerous Conditions - pathology</subject><subject>Tomography, X-Ray Computed</subject><subject>von Meyenburg complex</subject><issn>1320-5463</issn><issn>1440-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMtOwzAQRS0Eorx-AXnFLsGxHdtBYoEqXqI8hGBtOe64pEriYhNo_56EVrBlNjPS3HtHcxDCGUmzvk7nacY5STJFZUoJUSmhVPB0uYX2fhfb_cwoSXIu2AjtxzgnJJNMkF00ypQkuZTZHrobv_natLPKWxNs1frGYBOqWLUzXLX407f4HlbQll2YYeubRQ1LiGf4GRY-fGDvsPNdwNZEiIdox5k6wtGmH6DXq8uX8U0yeby-HV9MEsuV4AkIywtGmTCQC6GYcyBLx0FBKabCGWnzkripZFBQS60snC0Vza2ihoJVlh2gk3XuIvj3DuKHbqpooe7_AN9FLQrOCkFYL1RroQ0-xgBOL0LVmLDSGdEDSD3XAy898NIDSP0DUi976_HmRlc2MP0zbsj1gvO14KuqYfXvYP10-zBM7BuasoK5</recordid><startdate>200808</startdate><enddate>200808</enddate><creator>Song, Joon Seon</creator><creator>Lee, Young‐Joo</creator><creator>Kim, Kyoung Won</creator><creator>Huh, Jooryung</creator><creator>Jang, Se Jin</creator><creator>Yu, Eunsil</creator><general>Blackwell Publishing Asia</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200808</creationdate><title>Cholangiocarcinoma arising in von Meyenburg complexes: Report of four cases</title><author>Song, Joon Seon ; Lee, Young‐Joo ; Kim, Kyoung Won ; Huh, Jooryung ; Jang, Se Jin ; Yu, Eunsil</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4864-e6c493236ae56683ffe7bf4e8eb6d6fa7c5b0fd73e92c2c79fcb825c82a2ec8c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Aged</topic><topic>Bile Duct Neoplasms - complications</topic><topic>Bile Duct Neoplasms - pathology</topic><topic>Bile Duct Neoplasms - surgery</topic><topic>Bile Ducts, Intrahepatic - pathology</topic><topic>Carcinoma, Hepatocellular - pathology</topic><topic>Cell Transformation, Neoplastic</topic><topic>cholangiocarcinoma</topic><topic>Cholangiocarcinoma - complications</topic><topic>Cholangiocarcinoma - pathology</topic><topic>Cholangiocarcinoma - surgery</topic><topic>cytokeratin 7</topic><topic>Disease-Free Survival</topic><topic>Fatal Outcome</topic><topic>Hamartoma - complications</topic><topic>Hamartoma - pathology</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Ki‐67 antigen</topic><topic>Liver Diseases - complications</topic><topic>Liver Diseases - pathology</topic><topic>Liver Neoplasms - pathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Precancerous Conditions - pathology</topic><topic>Tomography, X-Ray Computed</topic><topic>von Meyenburg complex</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Song, Joon Seon</creatorcontrib><creatorcontrib>Lee, Young‐Joo</creatorcontrib><creatorcontrib>Kim, Kyoung Won</creatorcontrib><creatorcontrib>Huh, Jooryung</creatorcontrib><creatorcontrib>Jang, Se Jin</creatorcontrib><creatorcontrib>Yu, Eunsil</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Pathology international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Song, Joon Seon</au><au>Lee, Young‐Joo</au><au>Kim, Kyoung Won</au><au>Huh, Jooryung</au><au>Jang, Se Jin</au><au>Yu, Eunsil</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cholangiocarcinoma arising in von Meyenburg complexes: Report of four cases</atitle><jtitle>Pathology international</jtitle><addtitle>Pathol Int</addtitle><date>2008-08</date><risdate>2008</risdate><volume>58</volume><issue>8</issue><spage>503</spage><epage>512</epage><pages>503-512</pages><issn>1320-5463</issn><eissn>1440-1827</eissn><abstract>Although von Meyenburg complexes (VMC) are largely considered to be innocuous, neoplastic transformations have been described. The present report describes four cases of cholangiocarcinoma (CC) occurring on a background of VMC. The patients were all male and aged 69, 59, 68 and 75 years, respectively. While two patients were asymptomatic, the other two had a history of colon cancer. Radiologically the tumors measured 3, 4, 4.5 and 10 cm and were well enhanced from the arterial to delayed portal phase. Microscopically, the tumor consisted of multiple foci of characteristic VMC, and had a gradual transition from VMC to hyperplasia or dysplasia and well‐ to moderately differentiated adenocarcinomas. One patient had combined hepatocellular carcinoma (HCC) and CC, occurring in the high grade dysplastic nodule and VMC. On immunohistochemistry the epithelial cells of the VMC and CC were immunopositive for cytokeratin (CK) 7 in three patients, with another patient being focally positive only for CK19. The Ki‐67 labeling indices increased from the VMC to the dysplastic areas and then to the carcinomas. As a potentially precancerous lesion, VMC should be carefully followed up in terms of any size increases. Thus, biopsies are essential to determine any proliferative epithelial changes including dysplasia and malignant transformation.</abstract><cop>Melbourne, Australia</cop><pub>Blackwell Publishing Asia</pub><pmid>18705771</pmid><doi>10.1111/j.1440-1827.2008.02264.x</doi><tpages>10</tpages></addata></record> |
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subjects | Aged Bile Duct Neoplasms - complications Bile Duct Neoplasms - pathology Bile Duct Neoplasms - surgery Bile Ducts, Intrahepatic - pathology Carcinoma, Hepatocellular - pathology Cell Transformation, Neoplastic cholangiocarcinoma Cholangiocarcinoma - complications Cholangiocarcinoma - pathology Cholangiocarcinoma - surgery cytokeratin 7 Disease-Free Survival Fatal Outcome Hamartoma - complications Hamartoma - pathology Humans Immunohistochemistry Ki‐67 antigen Liver Diseases - complications Liver Diseases - pathology Liver Neoplasms - pathology Male Middle Aged Precancerous Conditions - pathology Tomography, X-Ray Computed von Meyenburg complex |
title | Cholangiocarcinoma arising in von Meyenburg complexes: Report of four cases |
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