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A rare case of combined thymoma and a multilocular thymic cyst discovered due to chest pain
BACKGROUND: A thymoma with chest pain and multilocular thymic cysts (MTCs) is very rare. CASE PRESENTATION: A 49-year-old man presented to another hospital complaining of an anterior chest pain. Chest computed tomography (CT) showed an anterior mediastinal tumor 60 × 30 × 55 mm in size. The boundary...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8266926/ https://www.ncbi.nlm.nih.gov/pubmed/34236557 http://dx.doi.org/10.1186/s40792-021-01243-2 |
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author | Yasuda, Kengo Kidokoro, Yoshiteru Makishima, Karen Matsui, Shinji Nakanishi, Atsuyuki Nozaka, Yuji Oshima, Yuki Kubouchi, Yasuaki Takagi, Yuzo Haruki, Tomohiro Nakamura, Hiroshige |
author_facet | Yasuda, Kengo Kidokoro, Yoshiteru Makishima, Karen Matsui, Shinji Nakanishi, Atsuyuki Nozaka, Yuji Oshima, Yuki Kubouchi, Yasuaki Takagi, Yuzo Haruki, Tomohiro Nakamura, Hiroshige |
author_sort | Yasuda, Kengo |
collection | PubMed |
description | BACKGROUND: A thymoma with chest pain and multilocular thymic cysts (MTCs) is very rare. CASE PRESENTATION: A 49-year-old man presented to another hospital complaining of an anterior chest pain. Chest computed tomography (CT) showed an anterior mediastinal tumor 60 × 30 × 55 mm in size. The boundary with the pericardium or left brachiocephalic vein seemed to be partially unclear while enhanced by the contrast medium, and so the tumor could have invaded them. No definitive diagnosis of myasthenia gravis was made although the serum anti-acetylcholine receptor antibody count was high. We performed an extended thymectomy with combined partial resection of left brachiocephalic vein, left upper lobe, and left phrenic nerve. He was discharged with no chest pain and no complications post-surgery. The tumor was pathologically type B2 thymoma with hemorrhage necrosis and MTCs, and we diagnosed Masaoka stage II because of no histological infiltration to the organs. CONCLUSIONS: We speculated that hemorrhagic necrosis due to infarction in tumor caused the inflammation to spread to the surrounding organs, which was related to the chest pain and the development of MTCs. |
format | Online Article Text |
id | pubmed-8266926 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-82669262021-07-20 A rare case of combined thymoma and a multilocular thymic cyst discovered due to chest pain Yasuda, Kengo Kidokoro, Yoshiteru Makishima, Karen Matsui, Shinji Nakanishi, Atsuyuki Nozaka, Yuji Oshima, Yuki Kubouchi, Yasuaki Takagi, Yuzo Haruki, Tomohiro Nakamura, Hiroshige Surg Case Rep Case Report BACKGROUND: A thymoma with chest pain and multilocular thymic cysts (MTCs) is very rare. CASE PRESENTATION: A 49-year-old man presented to another hospital complaining of an anterior chest pain. Chest computed tomography (CT) showed an anterior mediastinal tumor 60 × 30 × 55 mm in size. The boundary with the pericardium or left brachiocephalic vein seemed to be partially unclear while enhanced by the contrast medium, and so the tumor could have invaded them. No definitive diagnosis of myasthenia gravis was made although the serum anti-acetylcholine receptor antibody count was high. We performed an extended thymectomy with combined partial resection of left brachiocephalic vein, left upper lobe, and left phrenic nerve. He was discharged with no chest pain and no complications post-surgery. The tumor was pathologically type B2 thymoma with hemorrhage necrosis and MTCs, and we diagnosed Masaoka stage II because of no histological infiltration to the organs. CONCLUSIONS: We speculated that hemorrhagic necrosis due to infarction in tumor caused the inflammation to spread to the surrounding organs, which was related to the chest pain and the development of MTCs. Springer Berlin Heidelberg 2021-07-08 /pmc/articles/PMC8266926/ /pubmed/34236557 http://dx.doi.org/10.1186/s40792-021-01243-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Case Report Yasuda, Kengo Kidokoro, Yoshiteru Makishima, Karen Matsui, Shinji Nakanishi, Atsuyuki Nozaka, Yuji Oshima, Yuki Kubouchi, Yasuaki Takagi, Yuzo Haruki, Tomohiro Nakamura, Hiroshige A rare case of combined thymoma and a multilocular thymic cyst discovered due to chest pain |
title | A rare case of combined thymoma and a multilocular thymic cyst discovered due to chest pain |
title_full | A rare case of combined thymoma and a multilocular thymic cyst discovered due to chest pain |
title_fullStr | A rare case of combined thymoma and a multilocular thymic cyst discovered due to chest pain |
title_full_unstemmed | A rare case of combined thymoma and a multilocular thymic cyst discovered due to chest pain |
title_short | A rare case of combined thymoma and a multilocular thymic cyst discovered due to chest pain |
title_sort | rare case of combined thymoma and a multilocular thymic cyst discovered due to chest pain |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8266926/ https://www.ncbi.nlm.nih.gov/pubmed/34236557 http://dx.doi.org/10.1186/s40792-021-01243-2 |
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