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Obstetrics & Gynecology 1972;39:263-268
© 1972 by The American College of Obstetricians and Gynecologists
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Bilateral Gonadoblastoma with Dysgerminoma

A Case Report

H. OLIVER WILLIAMSON, MD, FACO and H. RAWLING PRATT-THOMAS, MD

Departments of Obstetrics and Gynecology and Pathology, Medical University of South Carolina, Charleston, SC 29401.

Abstract

The clinical and pathologic features of a 19-year-old patient with dysgerminoma and bilateral gonadoblastoma are described. One of the gonadoblastomas and the dysgerminoma arose in a gonad of indeterminate nature. The other gonadoblastoma arose in a gonadal streak. The patient had a 46, XY chromosome karyotype and evidence of androgenic and estrogenic activity. After ablation of the pelvic organs, she has remained well for 4 years.






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