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(Chest. 1969;56:543-546.)
© 1969 American College of Chest Physicians

Primary Mediastinal Choriocarcinoma

S. Prusty M.S.1; J. N. Bhayana M.D.1; N. C. Nayak M.D.2; S. Singh M.S.1; V. S. Singh M.S.1; S. R. Sharma M.D.1; and P. P. Goel M.D.1

1 Department of Cardiothoracic Surgery, M. A. M. College and associated Irwin and G. B. Pant Hospitals, New Delhi, India
2 Associate Professor of Pathology, All India Institute of Medical Sciences

Primary mediastinal choriocarcinoma is a rare entity and is peculiar only to man. Although rigid criteria such as serial biopsies of the gonads are essential to rule out the possibility of such mediastinal tumor as a metastatic lesion, a review of the literature shows that anterior medlastinum is rarely involved by the metastasis from gonadal tumors. The clinical diagnosis of such a tumor can be made by the presence of the triad of chest pain, cough and gynecomastia in a man in the third decade. The prognosis of such a lesion is uniformly hopeless irrespective of the mode of treatment. A case of primary medlastinal choriocarcinoma in a 22-year-old man has been described. This case brings the total number of cases to 16.







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