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Intrathoracic lipoma of the chest wall that appeared relatively rapidly and could be resected and diagnosed by minimally invasive thoracoscopic surgery: A case report
The occurrence of lipoma in the thoracic cavity is relatively rare, and it is clinically difficult to distinguish it from liposarcoma. We report a case of intrathoracic lipoma that was pathologically diagnosed and differentiated from liposarcoma after minimally invasive thoracoscopic tumour resectio...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8987489/ https://www.ncbi.nlm.nih.gov/pubmed/35414936 http://dx.doi.org/10.1002/rcr2.946 |
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author | Hirai, Yoshimitsu Mikasa, Yurina Iguchi, Hideto Fusamoto, Aya Yata, Yumi Ohashi, Takuya Nishimura, Yoshiharu |
author_facet | Hirai, Yoshimitsu Mikasa, Yurina Iguchi, Hideto Fusamoto, Aya Yata, Yumi Ohashi, Takuya Nishimura, Yoshiharu |
author_sort | Hirai, Yoshimitsu |
collection | PubMed |
description | The occurrence of lipoma in the thoracic cavity is relatively rare, and it is clinically difficult to distinguish it from liposarcoma. We report a case of intrathoracic lipoma that was pathologically diagnosed and differentiated from liposarcoma after minimally invasive thoracoscopic tumour resection. A 35‐year‐old male patient without any symptoms was referred to our hospital due to an abnormal shadow on chest x‐ray. Computed tomography showed a low‐attenuated round‐shaped mass of 3.6 cm × 2.3 cm in diameter in the left chest wall. On magnetic resonance imaging, the mass was displayed as a high, high and low signal mass on T1‐weighted imaging (WI), T2WI and T2WI with fat suppression, respectively. We suspected a chest wall‐type lipoma, but because it appeared in a relatively short period of time and we thought it could be liposarcoma, we performed minimally invasive thoracoscopic surgery for diagnosis and treatment. The tumour was a stalked tumour with a capsule, contiguous to the wall pleura with only a single cord‐like structure. The majority of the tumour was found free in the pleural cavity. The tumour was diagnosed as a lipoma by histopathological examination. |
format | Online Article Text |
id | pubmed-8987489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-89874892022-04-11 Intrathoracic lipoma of the chest wall that appeared relatively rapidly and could be resected and diagnosed by minimally invasive thoracoscopic surgery: A case report Hirai, Yoshimitsu Mikasa, Yurina Iguchi, Hideto Fusamoto, Aya Yata, Yumi Ohashi, Takuya Nishimura, Yoshiharu Respirol Case Rep Case Reports The occurrence of lipoma in the thoracic cavity is relatively rare, and it is clinically difficult to distinguish it from liposarcoma. We report a case of intrathoracic lipoma that was pathologically diagnosed and differentiated from liposarcoma after minimally invasive thoracoscopic tumour resection. A 35‐year‐old male patient without any symptoms was referred to our hospital due to an abnormal shadow on chest x‐ray. Computed tomography showed a low‐attenuated round‐shaped mass of 3.6 cm × 2.3 cm in diameter in the left chest wall. On magnetic resonance imaging, the mass was displayed as a high, high and low signal mass on T1‐weighted imaging (WI), T2WI and T2WI with fat suppression, respectively. We suspected a chest wall‐type lipoma, but because it appeared in a relatively short period of time and we thought it could be liposarcoma, we performed minimally invasive thoracoscopic surgery for diagnosis and treatment. The tumour was a stalked tumour with a capsule, contiguous to the wall pleura with only a single cord‐like structure. The majority of the tumour was found free in the pleural cavity. The tumour was diagnosed as a lipoma by histopathological examination. John Wiley & Sons, Ltd 2022-04-07 /pmc/articles/PMC8987489/ /pubmed/35414936 http://dx.doi.org/10.1002/rcr2.946 Text en © 2022 The Authors. Respirology Case Reports published by John Wiley & Sons Australia, Ltd on behalf of The Asian Pacific Society of Respirology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Hirai, Yoshimitsu Mikasa, Yurina Iguchi, Hideto Fusamoto, Aya Yata, Yumi Ohashi, Takuya Nishimura, Yoshiharu Intrathoracic lipoma of the chest wall that appeared relatively rapidly and could be resected and diagnosed by minimally invasive thoracoscopic surgery: A case report |
title | Intrathoracic lipoma of the chest wall that appeared relatively rapidly and could be resected and diagnosed by minimally invasive thoracoscopic surgery: A case report |
title_full | Intrathoracic lipoma of the chest wall that appeared relatively rapidly and could be resected and diagnosed by minimally invasive thoracoscopic surgery: A case report |
title_fullStr | Intrathoracic lipoma of the chest wall that appeared relatively rapidly and could be resected and diagnosed by minimally invasive thoracoscopic surgery: A case report |
title_full_unstemmed | Intrathoracic lipoma of the chest wall that appeared relatively rapidly and could be resected and diagnosed by minimally invasive thoracoscopic surgery: A case report |
title_short | Intrathoracic lipoma of the chest wall that appeared relatively rapidly and could be resected and diagnosed by minimally invasive thoracoscopic surgery: A case report |
title_sort | intrathoracic lipoma of the chest wall that appeared relatively rapidly and could be resected and diagnosed by minimally invasive thoracoscopic surgery: a case report |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8987489/ https://www.ncbi.nlm.nih.gov/pubmed/35414936 http://dx.doi.org/10.1002/rcr2.946 |
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