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Rupture of thymoma due to recurrent tumor hemorrhage: a case report
BACKGROUND: Rupture of a thymoma is rare, and due to its rarity, the mechanism of rupture remains unclear. Here we report a case of a ruptured thymoma that ruptured due to an increase in the intratumoral pressure caused by recurrent hemorrhaging. CASE DESCRIPTION: A 70-year-old woman presented 2 day...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10364012/ https://www.ncbi.nlm.nih.gov/pubmed/37492796 http://dx.doi.org/10.21037/acr-23-44 |
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author | Uebayashi, Asuka Ema, Toshinari Oiwa, Hiroaki Yasuda, Kazuyo Matsubara, Osamu Funai, Kazuhito |
author_facet | Uebayashi, Asuka Ema, Toshinari Oiwa, Hiroaki Yasuda, Kazuyo Matsubara, Osamu Funai, Kazuhito |
author_sort | Uebayashi, Asuka |
collection | PubMed |
description | BACKGROUND: Rupture of a thymoma is rare, and due to its rarity, the mechanism of rupture remains unclear. Here we report a case of a ruptured thymoma that ruptured due to an increase in the intratumoral pressure caused by recurrent hemorrhaging. CASE DESCRIPTION: A 70-year-old woman presented 2 days prior persistent right chest and shoulder pain. A chest computed tomography (CT) scan revealed the presence of a mass occupying the anterior mediastinum and a right pleural effusion. It was diagnosed as an anterior mediastinum tumor. The increase in the levels of inflammatory markers and tumor necrosis observed on CT were suggestive of infection. As the general status of the patient was stable and she initially received antibiotic medical therapy, an improvement in the inflammatory marker levels was observed with antibiotic therapy. A surgical resection was performed 10 days after admission. Median sternotomy revealed a tumor extending from the mediastinum to the right thoracic cavity. Since the adhesion was strong and tumor invasion was suspected, the tumor was completely resected by combining a partial resection of the right middle and lower lobes with the pericardium. Pathological examination revealed that the tumor was a type B2 thymoma with fibrosis, necrosis, hemosiderosis, and hemorrhaging, suggesting recurrent hemorrhaging within the tumor. CONCLUSIONS: Based on the findings of our case, recurrent hemorrhaging within the tumor led to an increase in the intratumoral pressure and chronic inflammation and necrosis weakened the tumor wall. These changes contributed to the subsequent rupture. |
format | Online Article Text |
id | pubmed-10364012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-103640122023-07-25 Rupture of thymoma due to recurrent tumor hemorrhage: a case report Uebayashi, Asuka Ema, Toshinari Oiwa, Hiroaki Yasuda, Kazuyo Matsubara, Osamu Funai, Kazuhito AME Case Rep Case Report BACKGROUND: Rupture of a thymoma is rare, and due to its rarity, the mechanism of rupture remains unclear. Here we report a case of a ruptured thymoma that ruptured due to an increase in the intratumoral pressure caused by recurrent hemorrhaging. CASE DESCRIPTION: A 70-year-old woman presented 2 days prior persistent right chest and shoulder pain. A chest computed tomography (CT) scan revealed the presence of a mass occupying the anterior mediastinum and a right pleural effusion. It was diagnosed as an anterior mediastinum tumor. The increase in the levels of inflammatory markers and tumor necrosis observed on CT were suggestive of infection. As the general status of the patient was stable and she initially received antibiotic medical therapy, an improvement in the inflammatory marker levels was observed with antibiotic therapy. A surgical resection was performed 10 days after admission. Median sternotomy revealed a tumor extending from the mediastinum to the right thoracic cavity. Since the adhesion was strong and tumor invasion was suspected, the tumor was completely resected by combining a partial resection of the right middle and lower lobes with the pericardium. Pathological examination revealed that the tumor was a type B2 thymoma with fibrosis, necrosis, hemosiderosis, and hemorrhaging, suggesting recurrent hemorrhaging within the tumor. CONCLUSIONS: Based on the findings of our case, recurrent hemorrhaging within the tumor led to an increase in the intratumoral pressure and chronic inflammation and necrosis weakened the tumor wall. These changes contributed to the subsequent rupture. AME Publishing Company 2023-07-18 /pmc/articles/PMC10364012/ /pubmed/37492796 http://dx.doi.org/10.21037/acr-23-44 Text en 2023 AME Case Reports. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Case Report Uebayashi, Asuka Ema, Toshinari Oiwa, Hiroaki Yasuda, Kazuyo Matsubara, Osamu Funai, Kazuhito Rupture of thymoma due to recurrent tumor hemorrhage: a case report |
title | Rupture of thymoma due to recurrent tumor hemorrhage: a case report |
title_full | Rupture of thymoma due to recurrent tumor hemorrhage: a case report |
title_fullStr | Rupture of thymoma due to recurrent tumor hemorrhage: a case report |
title_full_unstemmed | Rupture of thymoma due to recurrent tumor hemorrhage: a case report |
title_short | Rupture of thymoma due to recurrent tumor hemorrhage: a case report |
title_sort | rupture of thymoma due to recurrent tumor hemorrhage: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10364012/ https://www.ncbi.nlm.nih.gov/pubmed/37492796 http://dx.doi.org/10.21037/acr-23-44 |
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