Multicentric angiomyolipoma in kidney, liver, and lymph node: case report/review of the literature

Detalhes bibliográficos
Autor(a) principal: Azevedo,Artur S. de
Data de Publicação: 2015
Outros Autores: Simão,Nábia Maria M. S.
Tipo de documento: Relatório
Idioma: eng
Título da fonte: Jornal Brasileiro de Patologia e Medicina Laboratorial (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442015000300173
Resumo: ABSTRACT Introduction: The angiomyolipoma (AML) is constituted by adipose tissue, blood vessels and smooth muscle fiber; follows a benign clinical course, with slow growth and absence of metastasis, occurring in tuberous sclerosis or sporadically. Objective: We intend to describe the clinical, radiological and histological aspects of this tumor. Case report: A-64-year-old woman presented with abdominal pain and dyspepsia. Tomography showed hepatic, renal and mesenteric nodules. Histological evaluation of mesenteric lymph node revealed perivascular epithelioid differentiation neoplasia, compatible with AML/perivascular epithelioid cell tumor (PEComa), positive for anti-S100, anti-human melanoma black-45 (HMB-45) and anti-smooth muscle actin. Conclusion: We described a rare AML with renal, hepatic and lymph node involvement, representing a multicenter version instead of metastasis.
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spelling Multicentric angiomyolipoma in kidney, liver, and lymph node: case report/review of the literatureangiomyolipomatuberous sclerosisperivascular epithelioid cell neoplasmsABSTRACT Introduction: The angiomyolipoma (AML) is constituted by adipose tissue, blood vessels and smooth muscle fiber; follows a benign clinical course, with slow growth and absence of metastasis, occurring in tuberous sclerosis or sporadically. Objective: We intend to describe the clinical, radiological and histological aspects of this tumor. Case report: A-64-year-old woman presented with abdominal pain and dyspepsia. Tomography showed hepatic, renal and mesenteric nodules. Histological evaluation of mesenteric lymph node revealed perivascular epithelioid differentiation neoplasia, compatible with AML/perivascular epithelioid cell tumor (PEComa), positive for anti-S100, anti-human melanoma black-45 (HMB-45) and anti-smooth muscle actin. Conclusion: We described a rare AML with renal, hepatic and lymph node involvement, representing a multicenter version instead of metastasis. Sociedade Brasileira de Patologia Clínica2015-06-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442015000300173Jornal Brasileiro de Patologia e Medicina Laboratorial v.51 n.3 2015reponame:Jornal Brasileiro de Patologia e Medicina Laboratorial (Online)instname:Sociedade Brasileira de Patologia (SBP)instacron:SBP10.5935/1676-2444.20150030info:eu-repo/semantics/openAccessAzevedo,Artur S. deSimão,Nábia Maria M. S.eng2015-07-27T00:00:00Zoai:scielo:S1676-24442015000300173Revistahttp://www.scielo.br/jbpmlhttps://old.scielo.br/oai/scielo-oai.php||jbpml@sbpc.org.br1678-47741676-2444opendoar:2015-07-27T00:00Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) - Sociedade Brasileira de Patologia (SBP)false
dc.title.none.fl_str_mv Multicentric angiomyolipoma in kidney, liver, and lymph node: case report/review of the literature
title Multicentric angiomyolipoma in kidney, liver, and lymph node: case report/review of the literature
spellingShingle Multicentric angiomyolipoma in kidney, liver, and lymph node: case report/review of the literature
Azevedo,Artur S. de
angiomyolipoma
tuberous sclerosis
perivascular epithelioid cell neoplasms
title_short Multicentric angiomyolipoma in kidney, liver, and lymph node: case report/review of the literature
title_full Multicentric angiomyolipoma in kidney, liver, and lymph node: case report/review of the literature
title_fullStr Multicentric angiomyolipoma in kidney, liver, and lymph node: case report/review of the literature
title_full_unstemmed Multicentric angiomyolipoma in kidney, liver, and lymph node: case report/review of the literature
title_sort Multicentric angiomyolipoma in kidney, liver, and lymph node: case report/review of the literature
author Azevedo,Artur S. de
author_facet Azevedo,Artur S. de
Simão,Nábia Maria M. S.
author_role author
author2 Simão,Nábia Maria M. S.
author2_role author
dc.contributor.author.fl_str_mv Azevedo,Artur S. de
Simão,Nábia Maria M. S.
dc.subject.por.fl_str_mv angiomyolipoma
tuberous sclerosis
perivascular epithelioid cell neoplasms
topic angiomyolipoma
tuberous sclerosis
perivascular epithelioid cell neoplasms
description ABSTRACT Introduction: The angiomyolipoma (AML) is constituted by adipose tissue, blood vessels and smooth muscle fiber; follows a benign clinical course, with slow growth and absence of metastasis, occurring in tuberous sclerosis or sporadically. Objective: We intend to describe the clinical, radiological and histological aspects of this tumor. Case report: A-64-year-old woman presented with abdominal pain and dyspepsia. Tomography showed hepatic, renal and mesenteric nodules. Histological evaluation of mesenteric lymph node revealed perivascular epithelioid differentiation neoplasia, compatible with AML/perivascular epithelioid cell tumor (PEComa), positive for anti-S100, anti-human melanoma black-45 (HMB-45) and anti-smooth muscle actin. Conclusion: We described a rare AML with renal, hepatic and lymph node involvement, representing a multicenter version instead of metastasis.
publishDate 2015
dc.date.none.fl_str_mv 2015-06-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/report
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format report
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442015000300173
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.5935/1676-2444.20150030
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv
Sociedade Brasileira de Patologia Clínica
publisher.none.fl_str_mv
Sociedade Brasileira de Patologia Clínica
dc.source.none.fl_str_mv Jornal Brasileiro de Patologia e Medicina Laboratorial v.51 n.3 2015
reponame:Jornal Brasileiro de Patologia e Medicina Laboratorial (Online)
instname:Sociedade Brasileira de Patologia (SBP)
instacron:SBP
instname_str Sociedade Brasileira de Patologia (SBP)
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institution SBP
reponame_str Jornal Brasileiro de Patologia e Medicina Laboratorial (Online)
collection Jornal Brasileiro de Patologia e Medicina Laboratorial (Online)
repository.name.fl_str_mv Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) - Sociedade Brasileira de Patologia (SBP)
repository.mail.fl_str_mv ||jbpml@sbpc.org.br
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