Granulosa-Theca Cell Tumors

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Abstract
The clinical features of 102 patients with granulosa cell, tjieca cell, or mixed granulosa-theca cell tumors are presented. This review supports the thesis that these neoplasms, although of a common cell origin, are identifiable as separate entities with characteristic courses. The outward manifestations which these tumors present initially are not diagnostic. The extent of the tumor is prognostically significant. The most effective treatment that can be provided is total abdominal hysterectomy and bilateral salpingo-oophorectomy.

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