Meigs Syndrome: Case Report

Detalhes bibliográficos
Autor(a) principal: Santos, Pedro Hugo Gouveia Azevedo dos
Data de Publicação: 2023
Outros Autores: Nunes, Paulo Henrique Silva, Lima, Letícia Raabe Mota de, Dias, Vinicius Quintanilha Gomes, Matos, Mariana Ferreira, Matos, Leandro Rodrigo Pereira de, Assunção, Robson Caetano Guedes, Castro Neto, Heládio Feitosa e
Tipo de documento: Artigo
Idioma: por
eng
spa
Título da fonte: Revista Brasileira de Cancerologia (Online)
Texto Completo: https://rbc.inca.gov.br/index.php/revista/article/view/3939
Resumo: Introduction: Meigs syndrome is a rare clinical condition, defined as the association of pleural effusion, ascites and ovarian fibroma, with resolution of symptoms after tumor resection. Case report: Female patient, 56 years old, with dry cough associated with hyporexia, weight loss and progressive dyspnea for one month. Chest X-ray and later chest tomography showed massive pleural effusion on the right. Thoracocentesis was performed with drainage of 2,500 ml of serous fluid, suggestive of exudate. On examination, a palpable mass was observed in the hypogastrium, with an upper limit in the umbilicus. Imaging exams show solid expansive formation of possible left ovarian origin and presence of ascitic fluid. The patient underwent total hysterectomy with bilateral salpingo-oophorectomy and resection of the pelvic mass. Intraoperatively, frozen section was suggestive of ovarian fibroma. Histopathological of the surgical specimen confirmed ovarian fibroma measuring 13.0 x 12.5 x 7.5 cm and cytopathological examination of the ascitic fluid was negative for neoplastic cells. The patient evolved in good general condition with resolution of the pleural effusion and ascites and continues without recurrence of symptoms. Conclusion: The definitive diagnosis is made by histological confirmation of ovarian fibroma and resolution of symptoms after removal of the tumor. Dyspnea may be the initial symptom and the CA-125 may be elevated. The prognosis is usually good and the chances of recurrence are minimal.
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spelling Meigs Syndrome: Case ReportSíndrome de Meigs: Informe de CasoSíndrome de Meigs: Relato de Casosíndrome de Meigsfibromaascitederrame pleuraloncologia cirúrgicaMeigs syndromefibromaascitespleural effusionsurgical oncologysíndrome de Meigsfibromaascitisderrame pleuraloncología quirúrgicaIntroduction: Meigs syndrome is a rare clinical condition, defined as the association of pleural effusion, ascites and ovarian fibroma, with resolution of symptoms after tumor resection. Case report: Female patient, 56 years old, with dry cough associated with hyporexia, weight loss and progressive dyspnea for one month. Chest X-ray and later chest tomography showed massive pleural effusion on the right. Thoracocentesis was performed with drainage of 2,500 ml of serous fluid, suggestive of exudate. On examination, a palpable mass was observed in the hypogastrium, with an upper limit in the umbilicus. Imaging exams show solid expansive formation of possible left ovarian origin and presence of ascitic fluid. The patient underwent total hysterectomy with bilateral salpingo-oophorectomy and resection of the pelvic mass. Intraoperatively, frozen section was suggestive of ovarian fibroma. Histopathological of the surgical specimen confirmed ovarian fibroma measuring 13.0 x 12.5 x 7.5 cm and cytopathological examination of the ascitic fluid was negative for neoplastic cells. The patient evolved in good general condition with resolution of the pleural effusion and ascites and continues without recurrence of symptoms. Conclusion: The definitive diagnosis is made by histological confirmation of ovarian fibroma and resolution of symptoms after removal of the tumor. Dyspnea may be the initial symptom and the CA-125 may be elevated. The prognosis is usually good and the chances of recurrence are minimal.Introducción: El síndrome de Meigs es una condición clínica rara, definida como la asociación de derrame pleural, ascitis y fibroma de ovario, con resolución de los síntomas después de la resección del tumor. Informe del caso: Paciente femenino de 56 años con tos seca asociada a hiporexia, pérdida de peso y disnea progresiva durante 1 mes de evolución. La radiografía de tórax y posterior tomografía de tórax mostró derrame pleural masivo en el lado derecho, se realizó toracocentesis con drenaje de 2.500 ml de líquido seroso, sugestivo de exudado. A la exploración se observa una masa palpable en hipogastrio, con límite superior en ombligo. Los exámenes de imagen muestran formación sólida expansiva de posible origen ovárico izquierdo y presencia de líquido ascítico. La paciente fue sometida a histerectomía total con salpingooforectomía bilateral y resección de la masa pélvica. Intraoperatoriamente, sección congelada sugestiva de fibroma de ovario. El histopatológico de la pieza quirúrgica confirmó fibroma de ovario de 13,0 x 12,5 x 7,5 cm y el examen citopatológico del líquido ascítico fue negativo para células neoplásicas. El paciente evolucionó en buen estado general con resolución del derrame pleural y ascitis y continúa sin recidiva de los síntomas. Conclusión: El diagnóstico definitivo se realiza mediante la confirmación histológica del fibroma de ovario y la resolución de los síntomas tras la extirpación del tumor. La disnea puede ser el síntoma inicial y el CA-125 puede estar elevado. El pronóstico suele ser bueno y las posibilidades de recurrencia son mínimas.Introdução: A síndrome de Meigs é uma condição clínica rara, definida como a associação de derrame pleural, ascite e fibroma ovariano, com resolução dos sintomas após a ressecção do tumor. Relato do caso: Paciente, sexo feminino, 56 anos, com tosse seca, associada à hiporexia, perda de peso e dispneia progressiva durante um mês. Radiografia de tórax e posteriormente tomografia de tórax mostraram derrame pleural volumoso à direita, sendo realizada toracocentese com drenagem de 2.500 ml de líquido seroso, sugestivo de exsudato. Ao exame, observou-se massa palpável em hipogástrio, com limite superior em cicatriz umbilical. Exames de imagem mostram formação expansiva sólida de possível origem ovariana esquerda e presença de líquido ascítico. A paciente foi submetida à histerectomia total com salpingo-ooforectomia bilateral e ressecção da massa pélvica. No intraoperatório, o exame por congelação foi sugestivo de fibroma ovariano. O histopatológico da peça cirúrgica confirmou fibroma ovariano medindo 13,0 x 12,5 x 7,5 cm e o exame citopatológico do líquido ascítico foi negativo para células neoplásicas. A paciente evoluiu em bom estado geral com resolução do derrame pleural e da ascite e segue sem recorrência dos sintomas. Conclusão: O diagnóstico definitivo é feito pela confirmação histológica de fibroma ovariano e resolução dos sintomas após a remoção da tumoração. A dispneia pode ser o sintoma inicial e o marcador tumoral CA-125 pode estar elevado. O prognóstico costuma ser bom e as chances de recidiva são mínimas.INCA2023-05-25info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionRelato de Casoapplication/pdfapplication/pdfapplication/pdftext/htmlhttps://rbc.inca.gov.br/index.php/revista/article/view/393910.32635/2176-9745.RBC.2023v69n2.3939Revista Brasileira de Cancerologia; Vol. 69 No. 2 (2023): Apr./May/June; e-253939Revista Brasileira de Cancerologia; Vol. 69 Núm. 2 (2023): abr./mayo/jun.; e-253939Revista Brasileira de Cancerologia; v. 69 n. 2 (2023): abr./maio/jun.; e-2539392176-9745reponame:Revista Brasileira de Cancerologia (Online)instname:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)instacron:INCAporengspahttps://rbc.inca.gov.br/index.php/revista/article/view/3939/2884https://rbc.inca.gov.br/index.php/revista/article/view/3939/3311https://rbc.inca.gov.br/index.php/revista/article/view/3939/3083https://rbc.inca.gov.br/index.php/revista/article/view/3939/2887Copyright (c) 2023 Revista Brasileira de Cancerologiahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessSantos, Pedro Hugo Gouveia Azevedo dosNunes, Paulo Henrique SilvaLima, Letícia Raabe Mota deDias, Vinicius Quintanilha GomesMatos, Mariana FerreiraMatos, Leandro Rodrigo Pereira deAssunção, Robson Caetano GuedesCastro Neto, Heládio Feitosa e2024-01-05T16:49:58Zoai:rbc.inca.gov.br:article/3939Revistahttps://rbc.inca.gov.br/index.php/revistaPUBhttps://rbc.inca.gov.br/index.php/revista/oairbc@inca.gov.br0034-71162176-9745opendoar:2024-01-05T16:49:58Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)false
dc.title.none.fl_str_mv Meigs Syndrome: Case Report
Síndrome de Meigs: Informe de Caso
Síndrome de Meigs: Relato de Caso
title Meigs Syndrome: Case Report
spellingShingle Meigs Syndrome: Case Report
Santos, Pedro Hugo Gouveia Azevedo dos
síndrome de Meigs
fibroma
ascite
derrame pleural
oncologia cirúrgica
Meigs syndrome
fibroma
ascites
pleural effusion
surgical oncology
síndrome de Meigs
fibroma
ascitis
derrame pleural
oncología quirúrgica
title_short Meigs Syndrome: Case Report
title_full Meigs Syndrome: Case Report
title_fullStr Meigs Syndrome: Case Report
title_full_unstemmed Meigs Syndrome: Case Report
title_sort Meigs Syndrome: Case Report
author Santos, Pedro Hugo Gouveia Azevedo dos
author_facet Santos, Pedro Hugo Gouveia Azevedo dos
Nunes, Paulo Henrique Silva
Lima, Letícia Raabe Mota de
Dias, Vinicius Quintanilha Gomes
Matos, Mariana Ferreira
Matos, Leandro Rodrigo Pereira de
Assunção, Robson Caetano Guedes
Castro Neto, Heládio Feitosa e
author_role author
author2 Nunes, Paulo Henrique Silva
Lima, Letícia Raabe Mota de
Dias, Vinicius Quintanilha Gomes
Matos, Mariana Ferreira
Matos, Leandro Rodrigo Pereira de
Assunção, Robson Caetano Guedes
Castro Neto, Heládio Feitosa e
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Santos, Pedro Hugo Gouveia Azevedo dos
Nunes, Paulo Henrique Silva
Lima, Letícia Raabe Mota de
Dias, Vinicius Quintanilha Gomes
Matos, Mariana Ferreira
Matos, Leandro Rodrigo Pereira de
Assunção, Robson Caetano Guedes
Castro Neto, Heládio Feitosa e
dc.subject.por.fl_str_mv síndrome de Meigs
fibroma
ascite
derrame pleural
oncologia cirúrgica
Meigs syndrome
fibroma
ascites
pleural effusion
surgical oncology
síndrome de Meigs
fibroma
ascitis
derrame pleural
oncología quirúrgica
topic síndrome de Meigs
fibroma
ascite
derrame pleural
oncologia cirúrgica
Meigs syndrome
fibroma
ascites
pleural effusion
surgical oncology
síndrome de Meigs
fibroma
ascitis
derrame pleural
oncología quirúrgica
description Introduction: Meigs syndrome is a rare clinical condition, defined as the association of pleural effusion, ascites and ovarian fibroma, with resolution of symptoms after tumor resection. Case report: Female patient, 56 years old, with dry cough associated with hyporexia, weight loss and progressive dyspnea for one month. Chest X-ray and later chest tomography showed massive pleural effusion on the right. Thoracocentesis was performed with drainage of 2,500 ml of serous fluid, suggestive of exudate. On examination, a palpable mass was observed in the hypogastrium, with an upper limit in the umbilicus. Imaging exams show solid expansive formation of possible left ovarian origin and presence of ascitic fluid. The patient underwent total hysterectomy with bilateral salpingo-oophorectomy and resection of the pelvic mass. Intraoperatively, frozen section was suggestive of ovarian fibroma. Histopathological of the surgical specimen confirmed ovarian fibroma measuring 13.0 x 12.5 x 7.5 cm and cytopathological examination of the ascitic fluid was negative for neoplastic cells. The patient evolved in good general condition with resolution of the pleural effusion and ascites and continues without recurrence of symptoms. Conclusion: The definitive diagnosis is made by histological confirmation of ovarian fibroma and resolution of symptoms after removal of the tumor. Dyspnea may be the initial symptom and the CA-125 may be elevated. The prognosis is usually good and the chances of recurrence are minimal.
publishDate 2023
dc.date.none.fl_str_mv 2023-05-25
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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10.32635/2176-9745.RBC.2023v69n2.3939
url https://rbc.inca.gov.br/index.php/revista/article/view/3939
identifier_str_mv 10.32635/2176-9745.RBC.2023v69n2.3939
dc.language.iso.fl_str_mv por
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spa
language por
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spa
dc.relation.none.fl_str_mv https://rbc.inca.gov.br/index.php/revista/article/view/3939/2884
https://rbc.inca.gov.br/index.php/revista/article/view/3939/3311
https://rbc.inca.gov.br/index.php/revista/article/view/3939/3083
https://rbc.inca.gov.br/index.php/revista/article/view/3939/2887
dc.rights.driver.fl_str_mv Copyright (c) 2023 Revista Brasileira de Cancerologia
https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2023 Revista Brasileira de Cancerologia
https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
text/html
dc.publisher.none.fl_str_mv INCA
publisher.none.fl_str_mv INCA
dc.source.none.fl_str_mv Revista Brasileira de Cancerologia; Vol. 69 No. 2 (2023): Apr./May/June; e-253939
Revista Brasileira de Cancerologia; Vol. 69 Núm. 2 (2023): abr./mayo/jun.; e-253939
Revista Brasileira de Cancerologia; v. 69 n. 2 (2023): abr./maio/jun.; e-253939
2176-9745
reponame:Revista Brasileira de Cancerologia (Online)
instname:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)
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instname_str Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)
instacron_str INCA
institution INCA
reponame_str Revista Brasileira de Cancerologia (Online)
collection Revista Brasileira de Cancerologia (Online)
repository.name.fl_str_mv Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)
repository.mail.fl_str_mv rbc@inca.gov.br
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