Meningeal tumor: A rare extrahepatic association in patients with polycystic liver disease enrolled for liver transplantation
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.3892/ol.2012.605 http://hdl.handle.net/11449/11155 |
Resumo: | In the present study, we described a rare association of polycystic liver disease (PCLD) with intracranial meningiomas in patients included on a liver transplant list, focusing on the diagnosis, treatment and possible association with any genetic alterations. Two female patients, aged 39 and 49 years were included on a liver transplant list due to extensive PCLD, with symptoms related to an abdominal compartmental syndrome. Screening for extrahepatic manifestation revealed a right frontal meningioma in the first patient, and a parietal posterior calcified meningioma in the second patient, measuring 1 and 7x3x2 cm in diameter, respectively. Following tumor removal, the histological pattern was compatible with fibrous and transitional meningioma, respectively. Cytogenetic studies conducted following surgery did not reveal any changes in metaphase chromosomes. The postoperative follow-up for the two patients was uneventful, without complications, with the patients remaining on a liver transplant waiting list. We conclude that screening for extrahepatic manifestations of PCLD is mandatory, as certain lesions require treatment prior to liver transplantation. The lack of a genetic or familial association between these two cases show they are likely to have occurred by chance, rather than representing a previously unrecognized association between polycystic liver disease and cranial meningioma. |
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Meningeal tumor: A rare extrahepatic association in patients with polycystic liver disease enrolled for liver transplantationmeningiomaliver transplantationpolycystic liver diseaseIn the present study, we described a rare association of polycystic liver disease (PCLD) with intracranial meningiomas in patients included on a liver transplant list, focusing on the diagnosis, treatment and possible association with any genetic alterations. Two female patients, aged 39 and 49 years were included on a liver transplant list due to extensive PCLD, with symptoms related to an abdominal compartmental syndrome. Screening for extrahepatic manifestation revealed a right frontal meningioma in the first patient, and a parietal posterior calcified meningioma in the second patient, measuring 1 and 7x3x2 cm in diameter, respectively. Following tumor removal, the histological pattern was compatible with fibrous and transitional meningioma, respectively. Cytogenetic studies conducted following surgery did not reveal any changes in metaphase chromosomes. The postoperative follow-up for the two patients was uneventful, without complications, with the patients remaining on a liver transplant waiting list. We conclude that screening for extrahepatic manifestations of PCLD is mandatory, as certain lesions require treatment prior to liver transplantation. The lack of a genetic or familial association between these two cases show they are likely to have occurred by chance, rather than representing a previously unrecognized association between polycystic liver disease and cranial meningioma.UNESP, Botucatu Fac Med, Div Gastrointestinal Transplant, Dept Surg, Botucatu, SP, BrazilUNESP, Botucatu Fac Med, Dept Neurosurg, Botucatu, SP, BrazilUNESP, Botucatu Fac Med, Dept Urol, Botucatu, SP, BrazilUNESP, Botucatu Fac Med, Div Gastrointestinal Transplant, Dept Surg, Botucatu, SP, BrazilUNESP, Botucatu Fac Med, Dept Neurosurg, Botucatu, SP, BrazilUNESP, Botucatu Fac Med, Dept Urol, Botucatu, SP, BrazilSpandidos Publ LtdUniversidade Estadual Paulista (Unesp)Bakonyi Neto, Alexandre [UNESP]Zanini, Marco Antonio [UNESP]Cavalheiro da Silva, Amanda Pinter [UNESP]Winckler, Camila [UNESP]Dos Santos, Rodrigo Mattos [UNESP]Furtado, Marcelo Lopes [UNESP]2014-05-20T13:32:40Z2014-05-20T13:32:40Z2012-05-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1007-1010http://dx.doi.org/10.3892/ol.2012.605Oncology Letters. Athens: Spandidos Publ Ltd, v. 3, n. 5, p. 1007-1010, 2012.1792-1074http://hdl.handle.net/11449/1115510.3892/ol.2012.605WOS:00030328140001072802171676420562894975141895189Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengOncology Letters1.6640,599info:eu-repo/semantics/openAccess2024-09-03T14:30:11Zoai:repositorio.unesp.br:11449/11155Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-03T14:30:11Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Meningeal tumor: A rare extrahepatic association in patients with polycystic liver disease enrolled for liver transplantation |
title |
Meningeal tumor: A rare extrahepatic association in patients with polycystic liver disease enrolled for liver transplantation |
spellingShingle |
Meningeal tumor: A rare extrahepatic association in patients with polycystic liver disease enrolled for liver transplantation Bakonyi Neto, Alexandre [UNESP] meningioma liver transplantation polycystic liver disease |
title_short |
Meningeal tumor: A rare extrahepatic association in patients with polycystic liver disease enrolled for liver transplantation |
title_full |
Meningeal tumor: A rare extrahepatic association in patients with polycystic liver disease enrolled for liver transplantation |
title_fullStr |
Meningeal tumor: A rare extrahepatic association in patients with polycystic liver disease enrolled for liver transplantation |
title_full_unstemmed |
Meningeal tumor: A rare extrahepatic association in patients with polycystic liver disease enrolled for liver transplantation |
title_sort |
Meningeal tumor: A rare extrahepatic association in patients with polycystic liver disease enrolled for liver transplantation |
author |
Bakonyi Neto, Alexandre [UNESP] |
author_facet |
Bakonyi Neto, Alexandre [UNESP] Zanini, Marco Antonio [UNESP] Cavalheiro da Silva, Amanda Pinter [UNESP] Winckler, Camila [UNESP] Dos Santos, Rodrigo Mattos [UNESP] Furtado, Marcelo Lopes [UNESP] |
author_role |
author |
author2 |
Zanini, Marco Antonio [UNESP] Cavalheiro da Silva, Amanda Pinter [UNESP] Winckler, Camila [UNESP] Dos Santos, Rodrigo Mattos [UNESP] Furtado, Marcelo Lopes [UNESP] |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Bakonyi Neto, Alexandre [UNESP] Zanini, Marco Antonio [UNESP] Cavalheiro da Silva, Amanda Pinter [UNESP] Winckler, Camila [UNESP] Dos Santos, Rodrigo Mattos [UNESP] Furtado, Marcelo Lopes [UNESP] |
dc.subject.por.fl_str_mv |
meningioma liver transplantation polycystic liver disease |
topic |
meningioma liver transplantation polycystic liver disease |
description |
In the present study, we described a rare association of polycystic liver disease (PCLD) with intracranial meningiomas in patients included on a liver transplant list, focusing on the diagnosis, treatment and possible association with any genetic alterations. Two female patients, aged 39 and 49 years were included on a liver transplant list due to extensive PCLD, with symptoms related to an abdominal compartmental syndrome. Screening for extrahepatic manifestation revealed a right frontal meningioma in the first patient, and a parietal posterior calcified meningioma in the second patient, measuring 1 and 7x3x2 cm in diameter, respectively. Following tumor removal, the histological pattern was compatible with fibrous and transitional meningioma, respectively. Cytogenetic studies conducted following surgery did not reveal any changes in metaphase chromosomes. The postoperative follow-up for the two patients was uneventful, without complications, with the patients remaining on a liver transplant waiting list. We conclude that screening for extrahepatic manifestations of PCLD is mandatory, as certain lesions require treatment prior to liver transplantation. The lack of a genetic or familial association between these two cases show they are likely to have occurred by chance, rather than representing a previously unrecognized association between polycystic liver disease and cranial meningioma. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-05-01 2014-05-20T13:32:40Z 2014-05-20T13:32:40Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.3892/ol.2012.605 Oncology Letters. Athens: Spandidos Publ Ltd, v. 3, n. 5, p. 1007-1010, 2012. 1792-1074 http://hdl.handle.net/11449/11155 10.3892/ol.2012.605 WOS:000303281400010 7280217167642056 2894975141895189 |
url |
http://dx.doi.org/10.3892/ol.2012.605 http://hdl.handle.net/11449/11155 |
identifier_str_mv |
Oncology Letters. Athens: Spandidos Publ Ltd, v. 3, n. 5, p. 1007-1010, 2012. 1792-1074 10.3892/ol.2012.605 WOS:000303281400010 7280217167642056 2894975141895189 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Oncology Letters 1.664 0,599 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1007-1010 |
dc.publisher.none.fl_str_mv |
Spandidos Publ Ltd |
publisher.none.fl_str_mv |
Spandidos Publ Ltd |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
_version_ |
1810021394302369792 |