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

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. H...

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Veröffentlicht in:Respiratory medicine case reports 2024-01, Vol.50, p.102037, Article 102037
Hauptverfasser: Matsuyama, Takahiro, Kubota, Koji, Tsuruzono, Kentaro, Uchida, Hiroko, Hamasaki, Tetsuro, Mizuno, Keiko, Inoue, Hiromasa
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Sprache:eng
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Zusammenfassung: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.
ISSN:2213-0071
2213-0071
DOI:10.1016/j.rmcr.2024.102037