Bilateral Sertoli-Leydig Cell Tumor in a Primigravida: A Rare Case
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چکیده
منابع مشابه
Bilateral Sertoli-Leydig Cell Tumor in a Primigravida: A Rare Case
We present a unique case of incidentally discovered bilateral Sertoli Leydig cell tumour in a primigravida who displayed no features of virilization. The apha fetoprotein levels were elevated. Magnetic resonance imaging was suggestive of ovarian tumors, possibly germ cell tumor. Bilateral salpingo-oophorectomy was performed and histopathology showed features of Sertoli Leydig cell tumor with in...
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Sertoli leydig cell tumors are exceedingly uncommon tumors of the ovary accounting for less than 0.5% of all ovarian neoplasms and 1% of sex cord tumors. These tumors are functional and secrete testosterone and only rarely they are estrogenic. Hence the patients present with virilization features. Most of the tumors are unilateral and bilaterality is extremely rare. Here we report an unusual ca...
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Leydig stromal cell tumor is a rare ovarian tumor that belongs to the group of sex-cord stromal tumors. They produce testosterone leading to hyperandrogenism. We present a 41yr old woman with symptoms of virilization and a mass of right adenex via ultra Sonography, and a rise of total and free serum testosterone. An ovarian source of androgen was suspected and a surgery performed. A diagnosis ...
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background: leydig cell tumor is a rare form of testicular neoplasm which comprises 1-3% of all testicular tumors and only about 3% of these tumors are bilateral. a few leydig all tumor have been described in patients with klinefelter�s syndrome so far. case: the patient described in this case report was a 24 year-old man with chief complaint of infertility for one year. physical examination, s...
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Mild hirsutism and alopecia in postmenopausal women can be a normal physiological response. Sex cord stromal tumors of ovary account for approximately 5-8% of all ovarian tumors. When hirsutism is accompanied by signs of virilization such as severe balding, deepening of voice or clitoromegaly, an underlying androgen-secreting tumor, that may be malignant must be ruled out. We report a rare case...
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ژورنال
عنوان ژورنال: Rare Tumors
سال: 2014
ISSN: 2036-3613,2036-3613
DOI: 10.4081/rt.2014.5408