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Unusual giant multilocular mesothelial cyst of mediastinum

BACKGROUND: Intrathoracic mesothelial cysts are congenital lesions induced by the abnormal development of the pericardial coelom. There have been a few reports of giant mesothelial cyst of the superior mediastinum, but the preferred treatment remains a controversial topic. We herein report a rare ca...

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Autores principales: Manabe, Takehiko, Oka, Soichi, Ono, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7527379/
https://www.ncbi.nlm.nih.gov/pubmed/33000344
http://dx.doi.org/10.1186/s40792-020-01011-8
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author Manabe, Takehiko
Oka, Soichi
Ono, Kenji
author_facet Manabe, Takehiko
Oka, Soichi
Ono, Kenji
author_sort Manabe, Takehiko
collection PubMed
description BACKGROUND: Intrathoracic mesothelial cysts are congenital lesions induced by the abnormal development of the pericardial coelom. There have been a few reports of giant mesothelial cyst of the superior mediastinum, but the preferred treatment remains a controversial topic. We herein report a rare case of successful removal of giant mesothelial cyst that was incidentally detected during a medical checkup. CASE PRESENTATION: A 53-year-old man with a feeling of mild chest tightness was referred to our hospital for the evaluation of an abnormal shadow of the mediastinum on chest X-ray. Computed tomography showed a multilocular, homogenous, large cyst in the superior mediastinum measuring 18 cm in size without contrast enhancement and with spotty calcification, and magnetic resonance imaging showed a low intensity on T1-weighted images and high intensity on T2-weighted images. Therefore, a cystic thymoma, thymic cyst, lymphangioma, cystic teratoma or pericardial cyst was suspected as the preoperative diagnosis. Despite mild symptoms, the patient underwent total thymectomy under median sternotomy for an appropriate diagnosis and treatment. The pathological diagnosis was giant multilocular mesothelial cyst. CONCLUSIONS: Intrathoracic mesothelial cyst is a benign cyst and generally asymptomatic, but can sometimes induce critical chest clinical symptoms if untreated, depending on its size. In our case, complete surgical resection and a detailed pathological evaluation was effective for making the appropriate diagnosis and delivering treatment. In addition, an immunohistological evaluation is effective for diagnosing mesothelial cysts when it is difficult to distinguish the cyst from other cystic lesions.
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spelling pubmed-75273792020-10-19 Unusual giant multilocular mesothelial cyst of mediastinum Manabe, Takehiko Oka, Soichi Ono, Kenji Surg Case Rep Case Report BACKGROUND: Intrathoracic mesothelial cysts are congenital lesions induced by the abnormal development of the pericardial coelom. There have been a few reports of giant mesothelial cyst of the superior mediastinum, but the preferred treatment remains a controversial topic. We herein report a rare case of successful removal of giant mesothelial cyst that was incidentally detected during a medical checkup. CASE PRESENTATION: A 53-year-old man with a feeling of mild chest tightness was referred to our hospital for the evaluation of an abnormal shadow of the mediastinum on chest X-ray. Computed tomography showed a multilocular, homogenous, large cyst in the superior mediastinum measuring 18 cm in size without contrast enhancement and with spotty calcification, and magnetic resonance imaging showed a low intensity on T1-weighted images and high intensity on T2-weighted images. Therefore, a cystic thymoma, thymic cyst, lymphangioma, cystic teratoma or pericardial cyst was suspected as the preoperative diagnosis. Despite mild symptoms, the patient underwent total thymectomy under median sternotomy for an appropriate diagnosis and treatment. The pathological diagnosis was giant multilocular mesothelial cyst. CONCLUSIONS: Intrathoracic mesothelial cyst is a benign cyst and generally asymptomatic, but can sometimes induce critical chest clinical symptoms if untreated, depending on its size. In our case, complete surgical resection and a detailed pathological evaluation was effective for making the appropriate diagnosis and delivering treatment. In addition, an immunohistological evaluation is effective for diagnosing mesothelial cysts when it is difficult to distinguish the cyst from other cystic lesions. Springer Berlin Heidelberg 2020-10-01 /pmc/articles/PMC7527379/ /pubmed/33000344 http://dx.doi.org/10.1186/s40792-020-01011-8 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Case Report
Manabe, Takehiko
Oka, Soichi
Ono, Kenji
Unusual giant multilocular mesothelial cyst of mediastinum
title Unusual giant multilocular mesothelial cyst of mediastinum
title_full Unusual giant multilocular mesothelial cyst of mediastinum
title_fullStr Unusual giant multilocular mesothelial cyst of mediastinum
title_full_unstemmed Unusual giant multilocular mesothelial cyst of mediastinum
title_short Unusual giant multilocular mesothelial cyst of mediastinum
title_sort unusual giant multilocular mesothelial cyst of mediastinum
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7527379/
https://www.ncbi.nlm.nih.gov/pubmed/33000344
http://dx.doi.org/10.1186/s40792-020-01011-8
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