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...

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Published inRespirology case reports Vol. 10; no. 5; pp. e0946 - n/a
Main Authors Hirai, Yoshimitsu, Mikasa, Yurina, Iguchi, Hideto, Fusamoto, Aya, Yata, Yumi, Ohashi, Takuya, Nishimura, Yoshiharu
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 01.05.2022
John Wiley & Sons, Inc
Wiley
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Summary: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. A relatively rare intrathoracic lipoma, which is clinically important to differentiate from liposarcoma, was diagnosed by minimally invasive thoracoscopic surgery.
Bibliography:ObjectType-Case Study-2
SourceType-Scholarly Journals-1
content type line 23
ObjectType-Report-1
Associate Editor: Michael Hsin
ISSN:2051-3380
2051-3380
DOI:10.1002/rcr2.946