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Type A thymoma with simultaneous solitary intrapulmonary metastasis: A case report
A 79‐year‐old woman was referred to our facility because of an abnormal chest shadow. Chest computed tomography (CT) showed a solitary right middle lung nodule with a maximum diameter of 3 mm and anterior mediastinal nodule with a maximum diameter of 21 mm. The lung nodule was suspected of being a p...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8201543/ https://www.ncbi.nlm.nih.gov/pubmed/33960662 http://dx.doi.org/10.1111/1759-7714.13975 |
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author | Tatematsu, Tsutomu Okuda, Katsuhiro Endo, Katsuhiko Hattori, Hideo Matsui, Takuya Oda, Risa Sakane, Tadashi Yokota, Keisuke Nakanishi, Ryoichi |
author_facet | Tatematsu, Tsutomu Okuda, Katsuhiro Endo, Katsuhiko Hattori, Hideo Matsui, Takuya Oda, Risa Sakane, Tadashi Yokota, Keisuke Nakanishi, Ryoichi |
author_sort | Tatematsu, Tsutomu |
collection | PubMed |
description | A 79‐year‐old woman was referred to our facility because of an abnormal chest shadow. Chest computed tomography (CT) showed a solitary right middle lung nodule with a maximum diameter of 3 mm and anterior mediastinal nodule with a maximum diameter of 21 mm. The lung nodule was suspected of being a primary lung cancer rather than a metastatic tumor because there were no primary malignant tumors, apart from an anterior mediastinal tumor visible on diagnostic imaging, including F(18) fluorodeoxyglucose‐positron emission tomography, and a solitary lung nodule. Partial lung resection by video‐assisted thoracoscopic surgery (VATS) was performed, and the intraoperative frozen section of the tumor tissue resulted in a diagnosis of carcinoid tumor. As a result, right middle lobectomy by VATS was performed. The final histological diagnosis of the permanent specimen was intrapulmonary type A thymoma. VATS thymectomy was performed three months later. The histological diagnosis was type A thymoma with intrapulmonary metastasis (Masaoka stage IVb). Additional therapy was not performed because complete resection was achieved. Follow‐up CT was performed once every six months after the operation. The patient has been followed up for one year without any further recurrence. |
format | Online Article Text |
id | pubmed-8201543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-82015432021-06-16 Type A thymoma with simultaneous solitary intrapulmonary metastasis: A case report Tatematsu, Tsutomu Okuda, Katsuhiro Endo, Katsuhiko Hattori, Hideo Matsui, Takuya Oda, Risa Sakane, Tadashi Yokota, Keisuke Nakanishi, Ryoichi Thorac Cancer Case Reports A 79‐year‐old woman was referred to our facility because of an abnormal chest shadow. Chest computed tomography (CT) showed a solitary right middle lung nodule with a maximum diameter of 3 mm and anterior mediastinal nodule with a maximum diameter of 21 mm. The lung nodule was suspected of being a primary lung cancer rather than a metastatic tumor because there were no primary malignant tumors, apart from an anterior mediastinal tumor visible on diagnostic imaging, including F(18) fluorodeoxyglucose‐positron emission tomography, and a solitary lung nodule. Partial lung resection by video‐assisted thoracoscopic surgery (VATS) was performed, and the intraoperative frozen section of the tumor tissue resulted in a diagnosis of carcinoid tumor. As a result, right middle lobectomy by VATS was performed. The final histological diagnosis of the permanent specimen was intrapulmonary type A thymoma. VATS thymectomy was performed three months later. The histological diagnosis was type A thymoma with intrapulmonary metastasis (Masaoka stage IVb). Additional therapy was not performed because complete resection was achieved. Follow‐up CT was performed once every six months after the operation. The patient has been followed up for one year without any further recurrence. John Wiley & Sons Australia, Ltd 2021-05-07 2021-06 /pmc/articles/PMC8201543/ /pubmed/33960662 http://dx.doi.org/10.1111/1759-7714.13975 Text en © 2021 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Tatematsu, Tsutomu Okuda, Katsuhiro Endo, Katsuhiko Hattori, Hideo Matsui, Takuya Oda, Risa Sakane, Tadashi Yokota, Keisuke Nakanishi, Ryoichi Type A thymoma with simultaneous solitary intrapulmonary metastasis: A case report |
title | Type A thymoma with simultaneous solitary intrapulmonary metastasis: A case report |
title_full | Type A thymoma with simultaneous solitary intrapulmonary metastasis: A case report |
title_fullStr | Type A thymoma with simultaneous solitary intrapulmonary metastasis: A case report |
title_full_unstemmed | Type A thymoma with simultaneous solitary intrapulmonary metastasis: A case report |
title_short | Type A thymoma with simultaneous solitary intrapulmonary metastasis: A case report |
title_sort | type a thymoma with simultaneous solitary intrapulmonary metastasis: a case report |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8201543/ https://www.ncbi.nlm.nih.gov/pubmed/33960662 http://dx.doi.org/10.1111/1759-7714.13975 |
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