Meningeal tumor: A rare extrahepatic association in patients with polycystic liver disease enrolled for liver transplantation

Detalhes bibliográficos
Autor(a) principal: Bakonyi Neto, Alexandre [UNESP]
Data de Publicação: 2012
Outros Autores: Zanini, Marco Antonio [UNESP], Cavalheiro da Silva, Amanda Pinter [UNESP], Winckler, Camila [UNESP], Dos Santos, Rodrigo Mattos [UNESP], Furtado, Marcelo Lopes [UNESP]
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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spelling 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
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