Recurrence of retroperitoneal localized perivascular epithelioid cell tumor two years after initial diagnosis: case report
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , |
Tipo de documento: | Relatório |
Idioma: | eng |
Título da fonte: | São Paulo medical journal (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802019000200206 |
Resumo: | ABSTRACT CONTEXT: Perivascular epithelioid cell tumors (PEComas) are rare mesenchymal tumors. Adjuvant radiotherapy and/or chemotherapy are administered according to the patient’s clinical characteristics. CASE REPORT: A 42-year-old female patient was operated to treat a retroperitoneal mass. The diagnosis was established as PEComa with benign behavior. Two years after the diagnosis, chest and abdominal computed tomography scans showed intra-abdominal recurrence and lymphangioleiomyomatosis in the lung. Treatment with everolimus was started. The disease stabilized in the third month of treatment, according to the response evaluation criteria in solid tumors. CONCLUSION: PEComas are tumors with unpredictable behavior. Therefore, these patients require long-term follow-up, even in cases of correct diagnosis and benign PEComa. |
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São Paulo medical journal (Online) |
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Recurrence of retroperitoneal localized perivascular epithelioid cell tumor two years after initial diagnosis: case reportPerivascular epithelioid cell neoplasmsRetroperitoneal neoplasmsAntineoplastic protocolsABSTRACT CONTEXT: Perivascular epithelioid cell tumors (PEComas) are rare mesenchymal tumors. Adjuvant radiotherapy and/or chemotherapy are administered according to the patient’s clinical characteristics. CASE REPORT: A 42-year-old female patient was operated to treat a retroperitoneal mass. The diagnosis was established as PEComa with benign behavior. Two years after the diagnosis, chest and abdominal computed tomography scans showed intra-abdominal recurrence and lymphangioleiomyomatosis in the lung. Treatment with everolimus was started. The disease stabilized in the third month of treatment, according to the response evaluation criteria in solid tumors. CONCLUSION: PEComas are tumors with unpredictable behavior. Therefore, these patients require long-term follow-up, even in cases of correct diagnosis and benign PEComa.Associação Paulista de Medicina - APM2019-04-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802019000200206Sao Paulo Medical Journal v.137 n.2 2019reponame:São Paulo medical journal (Online)instname:Associação Paulista de Medicinainstacron:APM10.1590/1516-3180.2017.0120050717info:eu-repo/semantics/openAccessCihan,Yasemin BenderliKut,EnginKoç,Alieng2019-07-10T00:00:00Zoai:scielo:S1516-31802019000200206Revistahttp://www.scielo.br/spmjhttps://old.scielo.br/oai/scielo-oai.phprevistas@apm.org.br1806-94601516-3180opendoar:2019-07-10T00:00São Paulo medical journal (Online) - Associação Paulista de Medicinafalse |
dc.title.none.fl_str_mv |
Recurrence of retroperitoneal localized perivascular epithelioid cell tumor two years after initial diagnosis: case report |
title |
Recurrence of retroperitoneal localized perivascular epithelioid cell tumor two years after initial diagnosis: case report |
spellingShingle |
Recurrence of retroperitoneal localized perivascular epithelioid cell tumor two years after initial diagnosis: case report Cihan,Yasemin Benderli Perivascular epithelioid cell neoplasms Retroperitoneal neoplasms Antineoplastic protocols |
title_short |
Recurrence of retroperitoneal localized perivascular epithelioid cell tumor two years after initial diagnosis: case report |
title_full |
Recurrence of retroperitoneal localized perivascular epithelioid cell tumor two years after initial diagnosis: case report |
title_fullStr |
Recurrence of retroperitoneal localized perivascular epithelioid cell tumor two years after initial diagnosis: case report |
title_full_unstemmed |
Recurrence of retroperitoneal localized perivascular epithelioid cell tumor two years after initial diagnosis: case report |
title_sort |
Recurrence of retroperitoneal localized perivascular epithelioid cell tumor two years after initial diagnosis: case report |
author |
Cihan,Yasemin Benderli |
author_facet |
Cihan,Yasemin Benderli Kut,Engin Koç,Ali |
author_role |
author |
author2 |
Kut,Engin Koç,Ali |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Cihan,Yasemin Benderli Kut,Engin Koç,Ali |
dc.subject.por.fl_str_mv |
Perivascular epithelioid cell neoplasms Retroperitoneal neoplasms Antineoplastic protocols |
topic |
Perivascular epithelioid cell neoplasms Retroperitoneal neoplasms Antineoplastic protocols |
description |
ABSTRACT CONTEXT: Perivascular epithelioid cell tumors (PEComas) are rare mesenchymal tumors. Adjuvant radiotherapy and/or chemotherapy are administered according to the patient’s clinical characteristics. CASE REPORT: A 42-year-old female patient was operated to treat a retroperitoneal mass. The diagnosis was established as PEComa with benign behavior. Two years after the diagnosis, chest and abdominal computed tomography scans showed intra-abdominal recurrence and lymphangioleiomyomatosis in the lung. Treatment with everolimus was started. The disease stabilized in the third month of treatment, according to the response evaluation criteria in solid tumors. CONCLUSION: PEComas are tumors with unpredictable behavior. Therefore, these patients require long-term follow-up, even in cases of correct diagnosis and benign PEComa. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-04-01 |
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=S1516-31802019000200206 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802019000200206 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/1516-3180.2017.0120050717 |
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 |
Associação Paulista de Medicina - APM |
publisher.none.fl_str_mv |
Associação Paulista de Medicina - APM |
dc.source.none.fl_str_mv |
Sao Paulo Medical Journal v.137 n.2 2019 reponame:São Paulo medical journal (Online) instname:Associação Paulista de Medicina instacron:APM |
instname_str |
Associação Paulista de Medicina |
instacron_str |
APM |
institution |
APM |
reponame_str |
São Paulo medical journal (Online) |
collection |
São Paulo medical journal (Online) |
repository.name.fl_str_mv |
São Paulo medical journal (Online) - Associação Paulista de Medicina |
repository.mail.fl_str_mv |
revistas@apm.org.br |
_version_ |
1754209266653200384 |