BMC Pulmonary Medicine (Jun 2022)

Type A thymoma: a rare cause of neoplastic cardiac tamponade with long-term survival

  • Mika Takashima,
  • Kozo Kagawa,
  • Toru Sawada,
  • Hiroyuki Hino,
  • Keishi Naruse,
  • Eiji Takeuchi,
  • Shoji Sakiyama,
  • Tsutomu Shinohara

DOI
https://doi.org/10.1186/s12890-022-02034-7
Journal volume & issue
Vol. 22, no. 1
pp. 1 – 5

Abstract

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Abstract Background The prognosis of thymoma with cardiac tamponade is generally poor. Most of the reported thymomas with cardiac tamponade were type B or type AB (mixed thymoma), and cardiac tamponade due to type A thymoma, which has a better prognosis compared to type B thymoma, is extremely rare. Case presentation We encountered a case of cardiac tamponade in a 71-year-old male. He visited our emergency department due to exacerbation of fatigue and dyspnea on exertion that lasted for two weeks. Chest imaging revealed a large amount of pericardial fluid and a contrast-enhanced tumor with calcification in the anterior mediastinum. The patient underwent thoracoscopic tumor biopsy and pathological examinations revealed type A thymoma. In this case, long-term disease-free survival (7.5 years) was achieved by multidisciplinary treatment (preoperative chemotherapy, surgical excision, and postoperative radiation therapy), in accordance with the histological type. Conclusions This case indicates that neoplastic cardiac tamponade, even in elderly patients, should not necessarily be regarded as a terminal cancer and requires a systematic investigation for underlying causes.

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