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A case of Meigs’ syndrome with preceding pericardial effusion in advance of pleural effusion
BACKGROUND: Meigs’ syndrome is defined as the presence of a benign ovarian tumor with pleural effusion and ascites that resolve after removal of the tumor. The pathogenesis of the production of ascites and pleural effusion in this syndrome remains unknown. Aside from pleural effusion and ascites, pe...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4862177/ https://www.ncbi.nlm.nih.gov/pubmed/27160723 http://dx.doi.org/10.1186/s12890-016-0241-1 |
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author | Okuda, Kenichi Noguchi, Satoshi Narumoto, Osamu Ikemura, Masako Yamauchi, Yasuhiro Tanaka, Goh Takai, Daiya Fukayama, Masashi Nagase, Takahide |
author_facet | Okuda, Kenichi Noguchi, Satoshi Narumoto, Osamu Ikemura, Masako Yamauchi, Yasuhiro Tanaka, Goh Takai, Daiya Fukayama, Masashi Nagase, Takahide |
author_sort | Okuda, Kenichi |
collection | PubMed |
description | BACKGROUND: Meigs’ syndrome is defined as the presence of a benign ovarian tumor with pleural effusion and ascites that resolve after removal of the tumor. The pathogenesis of the production of ascites and pleural effusion in this syndrome remains unknown. Aside from pleural effusion and ascites, pericardial effusion is rarely observed in Meigs’ syndrome. Here, we report the first case of Meigs’ syndrome with preceding pericardial effusion in advance of pleural effusion. CASE PRESENTATION: An 84-year-old Japanese non-smoking woman with a history of lung cancer, treated by surgery, was admitted due to gradual worsening of dyspnea that had occurred over the previous month. She had asymptomatic and unchanging pericardial effusion and a pelvic mass, which had been detected 3 and 11 years previously, respectively. The patient was radiologically followed-up without the need for treatment. Two months before admission, the patient underwent a right upper lobectomy for localized lung adenocarcinoma and intraoperative pericardial fenestration confirmed that the pericardial effusion was not malignant. However, she began to experience dyspnea on exertion leading to admission. A chest, abdomen, and pelvis computed tomography scan confirmed the presence of right-sided pleural and pericardial effusion and ascites with a left ovarian mass. Repeated thoracentesis produced cultures that were negative for any microorganism and no malignant cells were detected in the pleural effusions. Pleural fluid accumulation persisted despite a tube thoracostomy for pleural effusion drainage. With a suspicion of Meigs’ syndrome, the patient underwent surgical resection of the ovarian mass and histopathological examination of the resected mass showed ovarian fibroma. Pleural and pericardial effusion as well as ascites resolved after tumor resection, confirming a diagnosis of Meigs’ syndrome. This clinical course suggests a strong association between pericardial effusion and ovarian fibroma, as well as pleural and peritoneal fluid. CONCLUSIONS: In female patients with unexplained pericardial effusion and an ovarian tumor, clinicians should consider the possibility of Meigs’ syndrome. Although a malignant disease should be suspected in all patients with undiagnosed pleural and/or pericardial effusion, Meigs’ syndrome is curable by tumor resection and should be differentiated from malignancy. |
format | Online Article Text |
id | pubmed-4862177 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48621772016-05-11 A case of Meigs’ syndrome with preceding pericardial effusion in advance of pleural effusion Okuda, Kenichi Noguchi, Satoshi Narumoto, Osamu Ikemura, Masako Yamauchi, Yasuhiro Tanaka, Goh Takai, Daiya Fukayama, Masashi Nagase, Takahide BMC Pulm Med Case Report BACKGROUND: Meigs’ syndrome is defined as the presence of a benign ovarian tumor with pleural effusion and ascites that resolve after removal of the tumor. The pathogenesis of the production of ascites and pleural effusion in this syndrome remains unknown. Aside from pleural effusion and ascites, pericardial effusion is rarely observed in Meigs’ syndrome. Here, we report the first case of Meigs’ syndrome with preceding pericardial effusion in advance of pleural effusion. CASE PRESENTATION: An 84-year-old Japanese non-smoking woman with a history of lung cancer, treated by surgery, was admitted due to gradual worsening of dyspnea that had occurred over the previous month. She had asymptomatic and unchanging pericardial effusion and a pelvic mass, which had been detected 3 and 11 years previously, respectively. The patient was radiologically followed-up without the need for treatment. Two months before admission, the patient underwent a right upper lobectomy for localized lung adenocarcinoma and intraoperative pericardial fenestration confirmed that the pericardial effusion was not malignant. However, she began to experience dyspnea on exertion leading to admission. A chest, abdomen, and pelvis computed tomography scan confirmed the presence of right-sided pleural and pericardial effusion and ascites with a left ovarian mass. Repeated thoracentesis produced cultures that were negative for any microorganism and no malignant cells were detected in the pleural effusions. Pleural fluid accumulation persisted despite a tube thoracostomy for pleural effusion drainage. With a suspicion of Meigs’ syndrome, the patient underwent surgical resection of the ovarian mass and histopathological examination of the resected mass showed ovarian fibroma. Pleural and pericardial effusion as well as ascites resolved after tumor resection, confirming a diagnosis of Meigs’ syndrome. This clinical course suggests a strong association between pericardial effusion and ovarian fibroma, as well as pleural and peritoneal fluid. CONCLUSIONS: In female patients with unexplained pericardial effusion and an ovarian tumor, clinicians should consider the possibility of Meigs’ syndrome. Although a malignant disease should be suspected in all patients with undiagnosed pleural and/or pericardial effusion, Meigs’ syndrome is curable by tumor resection and should be differentiated from malignancy. BioMed Central 2016-05-10 /pmc/articles/PMC4862177/ /pubmed/27160723 http://dx.doi.org/10.1186/s12890-016-0241-1 Text en © Okuda et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Okuda, Kenichi Noguchi, Satoshi Narumoto, Osamu Ikemura, Masako Yamauchi, Yasuhiro Tanaka, Goh Takai, Daiya Fukayama, Masashi Nagase, Takahide A case of Meigs’ syndrome with preceding pericardial effusion in advance of pleural effusion |
title | A case of Meigs’ syndrome with preceding pericardial effusion in advance of pleural effusion |
title_full | A case of Meigs’ syndrome with preceding pericardial effusion in advance of pleural effusion |
title_fullStr | A case of Meigs’ syndrome with preceding pericardial effusion in advance of pleural effusion |
title_full_unstemmed | A case of Meigs’ syndrome with preceding pericardial effusion in advance of pleural effusion |
title_short | A case of Meigs’ syndrome with preceding pericardial effusion in advance of pleural effusion |
title_sort | case of meigs’ syndrome with preceding pericardial effusion in advance of pleural effusion |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4862177/ https://www.ncbi.nlm.nih.gov/pubmed/27160723 http://dx.doi.org/10.1186/s12890-016-0241-1 |
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