Auxiliary partial orthotopic liver transplantation for acute liver failure in two children
: Acute liver failure in children and adults is associated with a high mortality rate. At present the treatment of choice is orthotopic whole‐liver transplantation. However, allogeneic liver transplantation necessitates lifelong immunosuppressive therapy, which is associated with substantial risks t...
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Veröffentlicht in: | Pediatric transplantation 1999-11, Vol.3 (4), p.328-332 |
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description | : Acute liver failure in children and adults is associated with a high mortality rate. At present the treatment of choice is orthotopic whole‐liver transplantation. However, allogeneic liver transplantation necessitates lifelong immunosuppressive therapy, which is associated with substantial risks to the patient. Temporary auxiliary partial orthotopic liver transplantation has been developed recently as an alternative, enabling the native liver to regenerate while avoiding the risks of long‐term immunosuppressive treatment. Here we describe two cases of partial orthotopic liver transplantation in children. Auxiliary partial orthotopic liver transplantation was performed in two boys (5 and 6 years old) suffering from acute liver failure of unknown origin. The native left lateral liver lobes (segment II and II) were removed and replaced by left lateral liver grafts from young blood‐group‐compatible adults. In the first child the native liver, which was 80% necrotic at time of transplantation, showed regeneration within two weeks and the partially necrotic graft could be surgically removed on day 15 after auxiliary transplantation. Four years after transplantation, the child is in excellent condition with normal liver function and does not require any treatment. In the second case the native liver (90% necrotic at time of transplantation) regenerated within 6 weeks of transplantation, at which time the transplanted liver was removed. The patient developed aplastic anemia and died 2 months after transplantation from candida sepsis. The conclusion was that auxiliary partial liver transplantation in childhood provides a valuable option to maintain liver function in acute liver failure until functional recovery of the native liver. The main advantage over whole‐liver transplantation is the chance to avoid lifelong immunosuppression. However, there is a higher surgical risk. Therefore, auxiliary transplantation should be considered carefully in every case of acute liver failure in children. |
doi_str_mv | 10.1034/j.1399-3046.1999.00060.x |
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At present the treatment of choice is orthotopic whole‐liver transplantation. However, allogeneic liver transplantation necessitates lifelong immunosuppressive therapy, which is associated with substantial risks to the patient. Temporary auxiliary partial orthotopic liver transplantation has been developed recently as an alternative, enabling the native liver to regenerate while avoiding the risks of long‐term immunosuppressive treatment. Here we describe two cases of partial orthotopic liver transplantation in children. Auxiliary partial orthotopic liver transplantation was performed in two boys (5 and 6 years old) suffering from acute liver failure of unknown origin. The native left lateral liver lobes (segment II and II) were removed and replaced by left lateral liver grafts from young blood‐group‐compatible adults. In the first child the native liver, which was 80% necrotic at time of transplantation, showed regeneration within two weeks and the partially necrotic graft could be surgically removed on day 15 after auxiliary transplantation. Four years after transplantation, the child is in excellent condition with normal liver function and does not require any treatment. In the second case the native liver (90% necrotic at time of transplantation) regenerated within 6 weeks of transplantation, at which time the transplanted liver was removed. The patient developed aplastic anemia and died 2 months after transplantation from candida sepsis. The conclusion was that auxiliary partial liver transplantation in childhood provides a valuable option to maintain liver function in acute liver failure until functional recovery of the native liver. The main advantage over whole‐liver transplantation is the chance to avoid lifelong immunosuppression. However, there is a higher surgical risk. Therefore, auxiliary transplantation should be considered carefully in every case of acute liver failure in children.</description><identifier>ISSN: 1397-3142</identifier><identifier>EISSN: 1399-3046</identifier><identifier>DOI: 10.1034/j.1399-3046.1999.00060.x</identifier><identifier>PMID: 10562979</identifier><language>eng</language><publisher>Copenhagen, Denmark: Munksgaard International Publishers</publisher><subject>acute liver failure - fulminant liver failure - liver transplantation - auxiliary liver transplantation - preschool - infant ; Adult ; Biological and medical sciences ; Biopsy ; Child ; Child, Preschool ; Drug Therapy, Combination ; Fatal Outcome ; Gastroenterology. Liver. Pancreas. Abdomen ; Glucocorticoids - therapeutic use ; Graft Rejection - enzymology ; Graft Rejection - pathology ; Graft Rejection - prevention & control ; Humans ; Immunosuppressive Agents - therapeutic use ; Liver Failure, Acute - blood ; Liver Failure, Acute - pathology ; Liver Failure, Acute - surgery ; Liver Transplantation - methods ; Liver Transplantation - pathology ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Medical sciences ; Other diseases. Semiology ; Risk Factors ; Tissue Donors ; Transaminases - blood</subject><ispartof>Pediatric transplantation, 1999-11, Vol.3 (4), p.328-332</ispartof><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3470-c3f5f0e508033b37c228aa4725ae97bd1e98cb38c8da3885b592ccb5781d54073</citedby><cites>FETCH-LOGICAL-c3470-c3f5f0e508033b37c228aa4725ae97bd1e98cb38c8da3885b592ccb5781d54073</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1034%2Fj.1399-3046.1999.00060.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1034%2Fj.1399-3046.1999.00060.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1985115$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10562979$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rodeck, Burkhard</creatorcontrib><creatorcontrib>Kardorff, Rüdiger</creatorcontrib><creatorcontrib>Melter, Michael</creatorcontrib><creatorcontrib>Schlitt, Hans J.</creatorcontrib><creatorcontrib>Oldhafer, Karl J.</creatorcontrib><title>Auxiliary partial orthotopic liver transplantation for acute liver failure in two children</title><title>Pediatric transplantation</title><addtitle>Pediatr Transplant</addtitle><description>: Acute liver failure in children and adults is associated with a high mortality rate. At present the treatment of choice is orthotopic whole‐liver transplantation. However, allogeneic liver transplantation necessitates lifelong immunosuppressive therapy, which is associated with substantial risks to the patient. Temporary auxiliary partial orthotopic liver transplantation has been developed recently as an alternative, enabling the native liver to regenerate while avoiding the risks of long‐term immunosuppressive treatment. Here we describe two cases of partial orthotopic liver transplantation in children. Auxiliary partial orthotopic liver transplantation was performed in two boys (5 and 6 years old) suffering from acute liver failure of unknown origin. The native left lateral liver lobes (segment II and II) were removed and replaced by left lateral liver grafts from young blood‐group‐compatible adults. In the first child the native liver, which was 80% necrotic at time of transplantation, showed regeneration within two weeks and the partially necrotic graft could be surgically removed on day 15 after auxiliary transplantation. Four years after transplantation, the child is in excellent condition with normal liver function and does not require any treatment. In the second case the native liver (90% necrotic at time of transplantation) regenerated within 6 weeks of transplantation, at which time the transplanted liver was removed. The patient developed aplastic anemia and died 2 months after transplantation from candida sepsis. The conclusion was that auxiliary partial liver transplantation in childhood provides a valuable option to maintain liver function in acute liver failure until functional recovery of the native liver. The main advantage over whole‐liver transplantation is the chance to avoid lifelong immunosuppression. However, there is a higher surgical risk. Therefore, auxiliary transplantation should be considered carefully in every case of acute liver failure in children.</description><subject>acute liver failure - fulminant liver failure - liver transplantation - auxiliary liver transplantation - preschool - infant</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Drug Therapy, Combination</subject><subject>Fatal Outcome</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Glucocorticoids - therapeutic use</subject><subject>Graft Rejection - enzymology</subject><subject>Graft Rejection - pathology</subject><subject>Graft Rejection - prevention & control</subject><subject>Humans</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Liver Failure, Acute - blood</subject><subject>Liver Failure, Acute - pathology</subject><subject>Liver Failure, Acute - surgery</subject><subject>Liver Transplantation - methods</subject><subject>Liver Transplantation - pathology</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Other diseases. Semiology</subject><subject>Risk Factors</subject><subject>Tissue Donors</subject><subject>Transaminases - blood</subject><issn>1397-3142</issn><issn>1399-3046</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1vFSEUhonR2A_9C4aFcTdTPoYBFi6aWluTpjamWuOGMAyTcuUOIzD29t_L7dzULruBk5zn5RweACBGNUa0OVrVmEpZUdS0NZZS1gihFtWbF2D_sfHyoeYVxQ3ZAwcprRDCbSOa12API9YSyeU--HU8b5x3Ot7DScfstIch5tuQw-QM9O6vjTBHPabJ6zHr7MIIhxChNnO2u_6gnZ-jhW6E-S5Ac-t8H-34BrwatE_27e4-BN8_n16fnFcXX8--nBxfVIY2HJVzYAOyDAlEaUe5IURo3XDCtJW867GVwnRUGNFrKgTrmCTGdIwL3LMGcXoIPizvTjH8mW3Kau2Ssb4sbMOcVCuJIITgAooFNDGkFO2gpujW5esKI7X1qlZqq09t9amtV_XgVW1K9N1uxtytbf8kuIgswPsdoJPRfijKjEv_OSkYxqxgHxfsznl7_-z56ur0-lupSr5a8i5lu3nM6_hbtZxypm4uz9TND8x_fuJIXdF_kbujuw</recordid><startdate>199911</startdate><enddate>199911</enddate><creator>Rodeck, Burkhard</creator><creator>Kardorff, Rüdiger</creator><creator>Melter, Michael</creator><creator>Schlitt, Hans J.</creator><creator>Oldhafer, Karl J.</creator><general>Munksgaard International Publishers</general><general>Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><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>199911</creationdate><title>Auxiliary partial orthotopic liver transplantation for acute liver failure in two children</title><author>Rodeck, Burkhard ; Kardorff, Rüdiger ; Melter, Michael ; Schlitt, Hans J. ; Oldhafer, Karl J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3470-c3f5f0e508033b37c228aa4725ae97bd1e98cb38c8da3885b592ccb5781d54073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>acute liver failure - fulminant liver failure - liver transplantation - auxiliary liver transplantation - preschool - infant</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Drug Therapy, Combination</topic><topic>Fatal Outcome</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Glucocorticoids - therapeutic use</topic><topic>Graft Rejection - enzymology</topic><topic>Graft Rejection - pathology</topic><topic>Graft Rejection - prevention & control</topic><topic>Humans</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Liver Failure, Acute - blood</topic><topic>Liver Failure, Acute - pathology</topic><topic>Liver Failure, Acute - surgery</topic><topic>Liver Transplantation - methods</topic><topic>Liver Transplantation - pathology</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Other diseases. Semiology</topic><topic>Risk Factors</topic><topic>Tissue Donors</topic><topic>Transaminases - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rodeck, Burkhard</creatorcontrib><creatorcontrib>Kardorff, Rüdiger</creatorcontrib><creatorcontrib>Melter, Michael</creatorcontrib><creatorcontrib>Schlitt, Hans J.</creatorcontrib><creatorcontrib>Oldhafer, Karl J.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><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>Pediatric transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rodeck, Burkhard</au><au>Kardorff, Rüdiger</au><au>Melter, Michael</au><au>Schlitt, Hans J.</au><au>Oldhafer, Karl J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Auxiliary partial orthotopic liver transplantation for acute liver failure in two children</atitle><jtitle>Pediatric transplantation</jtitle><addtitle>Pediatr Transplant</addtitle><date>1999-11</date><risdate>1999</risdate><volume>3</volume><issue>4</issue><spage>328</spage><epage>332</epage><pages>328-332</pages><issn>1397-3142</issn><eissn>1399-3046</eissn><abstract>: Acute liver failure in children and adults is associated with a high mortality rate. At present the treatment of choice is orthotopic whole‐liver transplantation. However, allogeneic liver transplantation necessitates lifelong immunosuppressive therapy, which is associated with substantial risks to the patient. Temporary auxiliary partial orthotopic liver transplantation has been developed recently as an alternative, enabling the native liver to regenerate while avoiding the risks of long‐term immunosuppressive treatment. Here we describe two cases of partial orthotopic liver transplantation in children. Auxiliary partial orthotopic liver transplantation was performed in two boys (5 and 6 years old) suffering from acute liver failure of unknown origin. The native left lateral liver lobes (segment II and II) were removed and replaced by left lateral liver grafts from young blood‐group‐compatible adults. In the first child the native liver, which was 80% necrotic at time of transplantation, showed regeneration within two weeks and the partially necrotic graft could be surgically removed on day 15 after auxiliary transplantation. Four years after transplantation, the child is in excellent condition with normal liver function and does not require any treatment. In the second case the native liver (90% necrotic at time of transplantation) regenerated within 6 weeks of transplantation, at which time the transplanted liver was removed. The patient developed aplastic anemia and died 2 months after transplantation from candida sepsis. The conclusion was that auxiliary partial liver transplantation in childhood provides a valuable option to maintain liver function in acute liver failure until functional recovery of the native liver. The main advantage over whole‐liver transplantation is the chance to avoid lifelong immunosuppression. However, there is a higher surgical risk. Therefore, auxiliary transplantation should be considered carefully in every case of acute liver failure in children.</abstract><cop>Copenhagen, Denmark</cop><pub>Munksgaard International Publishers</pub><pmid>10562979</pmid><doi>10.1034/j.1399-3046.1999.00060.x</doi><tpages>5</tpages></addata></record> |
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subjects | acute liver failure - fulminant liver failure - liver transplantation - auxiliary liver transplantation - preschool - infant Adult Biological and medical sciences Biopsy Child Child, Preschool Drug Therapy, Combination Fatal Outcome Gastroenterology. Liver. Pancreas. Abdomen Glucocorticoids - therapeutic use Graft Rejection - enzymology Graft Rejection - pathology Graft Rejection - prevention & control Humans Immunosuppressive Agents - therapeutic use Liver Failure, Acute - blood Liver Failure, Acute - pathology Liver Failure, Acute - surgery Liver Transplantation - methods Liver Transplantation - pathology Liver. Biliary tract. Portal circulation. Exocrine pancreas Male Medical sciences Other diseases. Semiology Risk Factors Tissue Donors Transaminases - blood |
title | Auxiliary partial orthotopic liver transplantation for acute liver failure in two children |
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