Rare benign neoplasms occur which are composed solely of Leydig cells derived from ovarian stroma rather than from preexisting hilus cells of the mesovarium. Two such tumors are described and two are noted in the literature although others, difficult to identify, undoubtedly exist. They are closely related to the stromal-Leydig cell tumor but are not multifocal and lack the thecoma-like stromal component. Both types of neoplasm occur in menopausal or post-menopausal women and are likely to be associated with masculinization. They are related to each other as the stromal luteoma is related to the partly luteinized theca cell tumor. The presence of crystalloids of Reinke in some of the lipid cells identifies the lipid cell component of the tumor as Leydig cells. Similar tumors lacking crystalloids, in fact, may be Leydig cell tumors but in the absence of definitive diagnostic criteria are best classified as lutein cell tumors.
DISTINCTIVE FORM OF OVARIAN LEYDICA cell tumor appears to be derived from the specific ovarian stroma and does not originate in preexisting hilus cells. It can be distinguished from the usual form of ovarian Leydig cell tumor that arises from the hilus,lo from the Sertoli-Leydig cell tumor, and also from another recently described ovarian tumor containing Leydig cells known as the stromal-Leydig cell tumor.1' In both of our cases, characteristic crystalloids of Reinke were identified within the tumor cells. T h e non-neoplastic portions of the ovaries showed stromal hyperplasia and contained foci of lutein-like stromal cells. We refer to this lesion as a pure Leydig cell tumor, nonhilar type.