Fine-needle aspiration cytology of primary granulosa cell tumor of the adrenal gland: A case report

✍ Scribed by Arif Hameed; Robert L. Coleman

• Publisher: John Wiley and Sons
• Year: 2000
• Tongue: English
• Weight: 132 KB
• Volume: 22
• Category: Article
• ISSN: 8755-1039
• DOI: 10.1002/(sici)1097-0339(200002)22:2<107::aid-dc10>3.0.co;2-1

✦ Synopsis

Extraovarian granulosa cell tumors are extremely rare. We report on a primary granulosa cell tumor of the adrenal gland. A 69-yr-old African-American female presented with a 1-yr history of irregular uterine bleeding and a palpable right abdominal mass. CT scan showed a 9.0-cm suprarenal mass as well as an enlarged uterus. CT-guided fine-needle aspiration (FNA) cytology of the adrenal mass was interpreted as a malignant neoplasm. She underwent exploratory laparotomy, right nephrectomy, and hysterectomy with bilateral salpingo-oophorectomy. The gross, histologic, and immunohistochemical findings of the adrenal mass were characteristic of a granulosa cell tumor. The uterus contained multiple leiomyomas. The endometrium showed simple hyperplasia. Both fallopian tubes and ovaries showed no pathologic abnormality. There was no evidence of tumor elsewhere. Although rare, extraovarian granulosa cell tumor should be considered in the differential diagnosis of adrenal tumors in women showing the FNA features described herein, especially when there is evidence of excessive estrogen production.