A rare case of combined thymoma and a multilocular thymic cyst discovered due to chest pain

Springer Science and Business Media LLC - Tập 7 - Trang 1-5 - 2021
Kengo Yasuda1,2, Yoshiteru Kidokoro2, Karen Makishima3, Shinji Matsui2,3, Atsuyuki Nakanishi2, Yuji Nozaka2, Yuki Oshima2,3, Yasuaki Kubouchi2, Yuzo Takagi2, Tomohiro Haruki2, Hiroshige Nakamura2
1Center for Clinical Residency Program, Tottori University Hospital, Tottori, Japan
2Division of General Thoracic Surgery and Breast and Endocrine Surgery, Department of Surgery, Faculty of Medicine, Tottori University, Tottori, Japan
3Department of Pathology, Faculty of Medicine, Tottori University, Tottori, Japan

Tóm tắt

A thymoma with chest pain and multilocular thymic cysts (MTCs) is very rare. 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. 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.

Tài liệu tham khảo

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