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
Hauptverfasser: Zhang, W, Jambulingam, P.S, Silva, M.A, Taniere, P, Bramhall, S.R, Mayer, A.D, Buckels, J.A.C, Mirza, D.F
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container_end_page 901
container_issue 7
container_start_page 898
container_title European journal of surgical oncology
container_volume 33
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 ; 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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.</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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