A rare metastatic choroidal tumor from primary mediastinal choriocarcinoma in a male is described. This tumor secreted gonadotrophins and showed the histopathologic characteristics of cytotrophoblast and syncytiotrophoblast cells. Early metastatic disease resulted in rapid death; the development of the choroidal metastatic lesion was diagnosed at autopsy.
|Original language||English (US)|
|Number of pages||7|
|Journal||Albrecht von Graefes Archiv für Klinische und Experimentelle Ophthalmologie|
|Publication status||Published - Sep 1 1978|
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