Meigs Syndrome: Case Report
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , , , |
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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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 info:eu-repo/semantics/publishedVersion Relato de Caso |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://rbc.inca.gov.br/index.php/revista/article/view/3939 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 eng spa |
language |
por eng spa |
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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 |
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application/pdf application/pdf application/pdf text/html |
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INCA |
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INCA |
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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) instacron:INCA |
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Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA) |
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INCA |
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INCA |
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Revista Brasileira de Cancerologia (Online) |
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Revista Brasileira de Cancerologia (Online) |
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Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA) |
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rbc@inca.gov.br |
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