Respiratory Medicine Case Reports (Jan 2024)

Primary mediastinal choriocarcinoma requiring differentiation from non-small cell lung cancer: An autopsy case report

  • Takahiro Matsuyama,
  • Koji Kubota,
  • Kentaro Tsuruzono,
  • Hiroko Uchida,
  • Tetsuro Hamasaki,
  • Keiko Mizuno,
  • Hiromasa Inoue

Journal volume & issue
Vol. 50
p. 102037

Abstract

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A 65-year-old man with dyspnea and hemoptysis presented with a right upper lobe mass associated with enlarged mediastinal lymph nodes and bilateral pulmonary nodules on chest computed tomography (CT), suspected lung cancer. Bronchial and CT-guided biopsies revealed poorly differentiated carcinoma. His condition deteriorated rapidly before a definitive diagnosis could be made. Autopsy revealed primary mediastinal choriocarcinoma. Primary mediastinal choriocarcinomas are rare, difficult to diagnose early and have a poor prognosis. In patients with a tumor expanding across the lung and mediastinum and exhibiting pathologic findings of a pooly differentiated carcinoma, we should consider choriocarcinoma, evaluating the serum β-human chorionic gonadotropin levels.

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