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Endocrine Care |
Institutes of Endocrinology (I.S., T.R.) and Pathology (D.N.), and Department of Neurosurgery (M.H.), Sheba Medical Center, Tel-Hashomer 52621; Fertility Unit (I.B.-H.) and Endocrinology Service (G.H.), Rabin Medical Center, Golda Campus, Petah Tikva 49372; and Department of Molecular Cell Biology (A.A.), The Weizmann Institute of Science, Rehovot 76100, Israel
Abstract
We report a unique case of a 28-yr-old woman with a
gonadotroph adenoma secreting FSH, presented with ovarian
hyperstimulation, without elevation of serum estradiol. She presented
with abdominal pain and large ovaries (both 10 cm in diameter) with
multiple follicular cysts shortly after discontinuing oral
contraceptive pills. She had a supranormal PRL level of 71 µg/liter
(normal, <20), FSH of 8.49.2 IU/liter (normal for follicular phase,
2.410), LH of 0.01 IU/liter (normal, 1.69.3), estradiol of 108
pmol/liter (normal for follicular phase, 80790), and free
-subunit
level of 0.11 µg/liter (normal, <1.8). A nuclear magnetic resonance
study revealed invasive pituitary macroadenoma, 30 mm in diameter.
Dopamine agonist (cabergoline) treatment normalized serum
PRL but had no affect on FSH levels. A transsphenoidal surgery was
performed, and most of the adenoma was resected. One month after
surgery the patient resumed menstruation, and the hormonal profile
included serum FSH of 6.3 IU/liter, LH of 2.1 IU/liter, estradiol of
156 pmol/liter, and PRL of 10 µg/liter. The excised adenoma tissue
exhibited intense immunostaining for FSH and secreted this hormone to
culture medium. Stimulation with TRH (both in vivo
preoperatively and in vitro study of the excised tumor)
had no effect on FSH secretion from the adenoma. Estradiol did not
suppress FSH release from cultured adenoma cells. Patient serum samples
showed significant FSH bioactivity when tested in a human granulosa
cell line.
This case is remarkable because the ovarian hyperstimulation related to the FSH-secreting adenoma was not associated with high levels of serum estradiol, probably due to insufficient LH production by the normal pituitary. Thus, it supports the two-cell, two-gonadotropin theory, that both FSH and LH are necessary for normal ovarian estrogen production.
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