Orthotopic liver transplantation for epithelioid haemangioendothelioma
Abstract Aims To report seven cases of epithelioid haemangioendothelioma (EHE) of the liver, a rare, low-grade malignant neoplasm of vascular origin that have been treated in our institution. Materials and methods Patients with ages ranging from 25 to 60 years presenting mainly with non-specific sym...
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Veröffentlicht in: | European journal of surgical oncology 2007-09, Vol.33 (7), p.898-901 |
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creator | Zhang, W Jambulingam, P.S Silva, M.A Taniere, P Bramhall, S.R Mayer, A.D Buckels, J.A.C Mirza, D.F |
description | Abstract Aims To report seven cases of epithelioid haemangioendothelioma (EHE) of the liver, a rare, low-grade malignant neoplasm of vascular origin that have been treated in our institution. Materials and methods Patients with ages ranging from 25 to 60 years presenting mainly with non-specific symptoms, such as right upper quadrant abdominal pain or weight loss. The tumours presented as multiple, nodular lesions involving both lobes of the liver. This type of tumour is often difficult to diagnose, with the final diagnosis being established only by histological examination. The key to diagnosis was the demonstration of cells containing factor VIII-related antigen. Results Five patients underwent orthotopic liver transplantation (OLT), four of whom are alive at a median follow up 38 months (11–88 months). One patient died of recurrent of disease at 88 months. Two patients did not receive an OLT since they presented with extrahepatic metastatic disease; they died at 21 and 25 months from diagnosis. Conclusion Orthotopic liver transplantation may be considered as a potentially curative treatment for this rare form of tumour when the disease is confined to the liver. |
doi_str_mv | 10.1016/j.ejso.2007.01.021 |
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Materials and methods Patients with ages ranging from 25 to 60 years presenting mainly with non-specific symptoms, such as right upper quadrant abdominal pain or weight loss. The tumours presented as multiple, nodular lesions involving both lobes of the liver. This type of tumour is often difficult to diagnose, with the final diagnosis being established only by histological examination. The key to diagnosis was the demonstration of cells containing factor VIII-related antigen. Results Five patients underwent orthotopic liver transplantation (OLT), four of whom are alive at a median follow up 38 months (11–88 months). One patient died of recurrent of disease at 88 months. Two patients did not receive an OLT since they presented with extrahepatic metastatic disease; they died at 21 and 25 months from diagnosis. Conclusion Orthotopic liver transplantation may be considered as a potentially curative treatment for this rare form of tumour when the disease is confined to the liver.</description><identifier>ISSN: 0748-7983</identifier><identifier>EISSN: 1532-2157</identifier><identifier>DOI: 10.1016/j.ejso.2007.01.021</identifier><identifier>PMID: 17331694</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adult ; Angiosarcoma ; Biomarkers, Tumor - metabolism ; Female ; Follow-Up Studies ; Haemangioma ; Hemangioendothelioma, Epithelioid - blood ; Hemangioendothelioma, Epithelioid - diagnosis ; Hemangioendothelioma, Epithelioid - surgery ; Hematology, Oncology and Palliative Medicine ; Humans ; Immunohistochemistry ; Liver Neoplasms - blood ; Liver Neoplasms - diagnosis ; Liver Neoplasms - surgery ; Liver Transplantation - methods ; Male ; Middle Aged ; Primary liver tumours ; Retrospective Studies ; Surgery ; Survival Rate ; Tomography, X-Ray Computed ; Treatment Outcome ; United Kingdom - epidemiology ; Vascular neoplasm of liver ; von Willebrand Factor - metabolism</subject><ispartof>European journal of surgical oncology, 2007-09, Vol.33 (7), p.898-901</ispartof><rights>Elsevier Ltd</rights><rights>2007 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c409t-8962b3537fff00889ee2985571782fe094ade754dd06570716aad69f2f8ac0823</citedby><cites>FETCH-LOGICAL-c409t-8962b3537fff00889ee2985571782fe094ade754dd06570716aad69f2f8ac0823</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ejso.2007.01.021$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,782,786,3554,27933,27934,46004</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17331694$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, W</creatorcontrib><creatorcontrib>Jambulingam, P.S</creatorcontrib><creatorcontrib>Silva, M.A</creatorcontrib><creatorcontrib>Taniere, P</creatorcontrib><creatorcontrib>Bramhall, S.R</creatorcontrib><creatorcontrib>Mayer, A.D</creatorcontrib><creatorcontrib>Buckels, J.A.C</creatorcontrib><creatorcontrib>Mirza, D.F</creatorcontrib><title>Orthotopic liver transplantation for epithelioid haemangioendothelioma</title><title>European journal of surgical oncology</title><addtitle>Eur J Surg Oncol</addtitle><description>Abstract Aims To report seven cases of epithelioid haemangioendothelioma (EHE) of the liver, a rare, low-grade malignant neoplasm of vascular origin that have been treated in our institution. Materials and methods Patients with ages ranging from 25 to 60 years presenting mainly with non-specific symptoms, such as right upper quadrant abdominal pain or weight loss. The tumours presented as multiple, nodular lesions involving both lobes of the liver. This type of tumour is often difficult to diagnose, with the final diagnosis being established only by histological examination. The key to diagnosis was the demonstration of cells containing factor VIII-related antigen. Results Five patients underwent orthotopic liver transplantation (OLT), four of whom are alive at a median follow up 38 months (11–88 months). One patient died of recurrent of disease at 88 months. Two patients did not receive an OLT since they presented with extrahepatic metastatic disease; they died at 21 and 25 months from diagnosis. Conclusion Orthotopic liver transplantation may be considered as a potentially curative treatment for this rare form of tumour when the disease is confined to the liver.</description><subject>Adult</subject><subject>Angiosarcoma</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Haemangioma</subject><subject>Hemangioendothelioma, Epithelioid - blood</subject><subject>Hemangioendothelioma, Epithelioid - diagnosis</subject><subject>Hemangioendothelioma, Epithelioid - surgery</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Liver Neoplasms - blood</subject><subject>Liver Neoplasms - diagnosis</subject><subject>Liver Neoplasms - surgery</subject><subject>Liver Transplantation - methods</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Primary liver tumours</subject><subject>Retrospective Studies</subject><subject>Surgery</subject><subject>Survival Rate</subject><subject>Tomography, X-Ray Computed</subject><subject>Treatment Outcome</subject><subject>United Kingdom - epidemiology</subject><subject>Vascular neoplasm of liver</subject><subject>von Willebrand Factor - metabolism</subject><issn>0748-7983</issn><issn>1532-2157</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUFr3DAQhUVpaTZp_0APxafe7I4k25KgFEpokkIghyZnoUijrlzbciVtIP--NrtQ6CGngeG9x8z3CPlAoaFA-89Dg0OODQMQDdAGGH1FdrTjrGa0E6_JDkQra6EkPyPnOQ8AoLhQb8kZFZzTXrU7cnWXyj6WuARbjeEJU1WSmfMymrmYEuJc-ZgqXELZ4xhicNXe4GTmXyHi7OJxO5l35I03Y8b3p3lBHq6-31_e1Ld31z8uv93WtgVVaql69sg7Lrz3AFIqRKZk1wkqJPMIqjUORdc6B30nQNDeGNcrz7w0FiTjF-TTMXdJ8c8Bc9FTyBbH9VyMh6x7yaAFSlchOwptijkn9HpJYTLpWVPQGz096I2e3uhpoHqlt5o-ntIPjxO6f5YTrlXw5SjA9cengElnG3C26EJCW7SL4eX8r__Z7RjmYM34G58xD_GQ5pWepjozDfrn1t9WH4i1Ot63_C_MOpYs</recordid><startdate>20070901</startdate><enddate>20070901</enddate><creator>Zhang, W</creator><creator>Jambulingam, P.S</creator><creator>Silva, M.A</creator><creator>Taniere, P</creator><creator>Bramhall, S.R</creator><creator>Mayer, A.D</creator><creator>Buckels, J.A.C</creator><creator>Mirza, D.F</creator><general>Elsevier Ltd</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>20070901</creationdate><title>Orthotopic liver transplantation for epithelioid haemangioendothelioma</title><author>Zhang, W ; Jambulingam, P.S ; Silva, M.A ; Taniere, P ; Bramhall, S.R ; Mayer, A.D ; Buckels, J.A.C ; Mirza, D.F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c409t-8962b3537fff00889ee2985571782fe094ade754dd06570716aad69f2f8ac0823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>Angiosarcoma</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Haemangioma</topic><topic>Hemangioendothelioma, Epithelioid - blood</topic><topic>Hemangioendothelioma, Epithelioid - diagnosis</topic><topic>Hemangioendothelioma, Epithelioid - surgery</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Liver Neoplasms - blood</topic><topic>Liver Neoplasms - diagnosis</topic><topic>Liver Neoplasms - surgery</topic><topic>Liver Transplantation - methods</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Primary liver tumours</topic><topic>Retrospective Studies</topic><topic>Surgery</topic><topic>Survival Rate</topic><topic>Tomography, X-Ray Computed</topic><topic>Treatment Outcome</topic><topic>United Kingdom - epidemiology</topic><topic>Vascular neoplasm of liver</topic><topic>von Willebrand Factor - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, W</creatorcontrib><creatorcontrib>Jambulingam, P.S</creatorcontrib><creatorcontrib>Silva, M.A</creatorcontrib><creatorcontrib>Taniere, P</creatorcontrib><creatorcontrib>Bramhall, S.R</creatorcontrib><creatorcontrib>Mayer, A.D</creatorcontrib><creatorcontrib>Buckels, J.A.C</creatorcontrib><creatorcontrib>Mirza, D.F</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>European journal of surgical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, W</au><au>Jambulingam, P.S</au><au>Silva, M.A</au><au>Taniere, P</au><au>Bramhall, S.R</au><au>Mayer, A.D</au><au>Buckels, J.A.C</au><au>Mirza, D.F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Orthotopic liver transplantation for epithelioid haemangioendothelioma</atitle><jtitle>European journal of surgical oncology</jtitle><addtitle>Eur J Surg Oncol</addtitle><date>2007-09-01</date><risdate>2007</risdate><volume>33</volume><issue>7</issue><spage>898</spage><epage>901</epage><pages>898-901</pages><issn>0748-7983</issn><eissn>1532-2157</eissn><abstract>Abstract Aims To report seven cases of epithelioid haemangioendothelioma (EHE) of the liver, a rare, low-grade malignant neoplasm of vascular origin that have been treated in our institution. Materials and methods Patients with ages ranging from 25 to 60 years presenting mainly with non-specific symptoms, such as right upper quadrant abdominal pain or weight loss. The tumours presented as multiple, nodular lesions involving both lobes of the liver. This type of tumour is often difficult to diagnose, with the final diagnosis being established only by histological examination. The key to diagnosis was the demonstration of cells containing factor VIII-related antigen. Results Five patients underwent orthotopic liver transplantation (OLT), four of whom are alive at a median follow up 38 months (11–88 months). One patient died of recurrent of disease at 88 months. Two patients did not receive an OLT since they presented with extrahepatic metastatic disease; they died at 21 and 25 months from diagnosis. Conclusion Orthotopic liver transplantation may be considered as a potentially curative treatment for this rare form of tumour when the disease is confined to the liver.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>17331694</pmid><doi>10.1016/j.ejso.2007.01.021</doi><tpages>4</tpages></addata></record> |
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subjects | Adult Angiosarcoma Biomarkers, Tumor - metabolism Female Follow-Up Studies Haemangioma Hemangioendothelioma, Epithelioid - blood Hemangioendothelioma, Epithelioid - diagnosis Hemangioendothelioma, Epithelioid - surgery Hematology, Oncology and Palliative Medicine Humans Immunohistochemistry Liver Neoplasms - blood Liver Neoplasms - diagnosis Liver Neoplasms - surgery Liver Transplantation - methods Male Middle Aged Primary liver tumours Retrospective Studies Surgery Survival Rate Tomography, X-Ray Computed Treatment Outcome United Kingdom - epidemiology Vascular neoplasm of liver von Willebrand Factor - metabolism |
title | Orthotopic liver transplantation for epithelioid haemangioendothelioma |
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