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Chinese Journal of Thoracic Surgery(Electronic Edition) ›› 2026, Vol. 13 ›› Issue (03): 231-236. doi: 10.3877/cma.j.issn.2095-8773.2026.03.09

• Case Report • Previous Articles    

Primary pulmonary choriocarcinoma: a case report and literature review

Hongbo Zhang1, Yichao Zhang1, Yi Chen2, Xinrui Song1, Jiaming Ju1, Tingting Huang1, Qirui Chen3, Xiangming Qiu1,†()   

  1. 1Department of Thoracic Surgery, Chinese People’s Armed Police Force Beijing Corps Hospital, Beijing 100027, China
    2Department of Pathology, Chinese People’s Armed Police Force Beijing Corps Hospital, Beijing 100027, China
    3Department of Thoracic Surgery, Beijing Chaoyang Hospital, Capital Medical University, Beijing 100027, China
  • Received:2026-05-07 Revised:2026-07-06 Accepted:2026-08-13 Online:2026-08-28 Published:2026-10-12
  • Contact: Xiangming Qiu

Abstract:

Primary pulmonary choriocarcinoma (PPC) is an extremely rare, highly malignant extragonadal epithelial neoplasm of non-gestational origin. As an aggressive trophoblastic tumor, it can secrete β-human chorionic gonadotropin (β-hCG). By reviewing domestic and foreign literature as well as recent research advances, this article analyzes the clinical manifestations, laboratory and imaging findings, pathological features, diagnosis and treatment regimens of one PPC case, and summarizes the characteristics of the disease. The aim is to improve clinicians’ understanding of PPC, reduce misdiagnosis and missed diagnosis, and standardize the diagnostic and therapeutic workflows for this disease.

Key words: Primary pulmonary choriocarcinoma, Choriocarcinoma, Lung neoplasms, Beta-human chorionic gonadotropin, Diagnosis, Therapeutics, Prognosis

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