Ph. Wang et al., STEROID CELL TUMORS OF THE OVARY - CLINICAL, ULTRASONIC, AND MRI DIAGNOSIS - A CASE-REPORT, European journal of radiology, 26(3), 1998, pp. 269-273
Steroid cell tumors of the ovary are rare sex-cord neoplasms which acc
ount for less than 0.1% of all ovarian tumors. They have been divided
into two subtypes according to their cell of origin as follows: stroma
l luteoma, and Leydig cell tumors, and a third subtype with lineage un
known is a steroid cell tumor, not otherwise specified (NOS). The clin
ical presentation may take many forms, including pain, abdominal diste
ntion and bloating, but perhaps the most interesting and noticeable pr
esentations are those related to the hormonal activity and virilizing
properties of the tumor. No radiological features of the steroid cell
tumor; NOS have been presented in the literature. This report presents
the MRI and ultrasonographic findings of a patient having steroid cel
l tumor, NOS, of the right ovary with metastasis to the uterus. (C) 19
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