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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...

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Autores principales: Yasuda, Kengo, Kidokoro, Yoshiteru, Makishima, Karen, Matsui, Shinji, Nakanishi, Atsuyuki, Nozaka, Yuji, Oshima, Yuki, Kubouchi, Yasuaki, Takagi, Yuzo, Haruki, Tomohiro, Nakamura, Hiroshige
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
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.
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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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