Affiliation:
1. Division of Endocrinology, Hospital Nacional Guillermo Almenara Irigoyen, Lima, PERU
2. Universidad Científica del Sur, Lima, PERU
3. Division of Endocrinology, Clínica Jesús del Norte, Lima, PERU
4. Division of Non-Communicable Diseases, Hospital de Apoyo Chepén, Chepén, PERU
5. Division of Anatomic Pathology, Hospital Nacional Guillermo Almenara Irigoyen, Lima, PERU
Abstract
<b>Introduction</b>: The virilizing ovarian tumors represent less than 1% of ovarian tumors, with the most common being Sertoli-Leydig cell tumor (SLCT). This stufy is a case series.<br />
<b>Methods: </b>We present the diagnosis, treatment, and evolution of 2 Peruvian women who developed virilization.<br />
<b>Results</b>: Case 1 is a 27-year-old woman with a history of polycystic ovary syndrome (PCOS), whose usual treatment was combined oral contraceptives, which she discontinued in the last year; she presented with voice changes, increased muscular strength, and acne of 6 months duration. Physical examination revealed only clitoromegaly. Tests showed elevated total testosterone, normal dehydroepiandrosterone sulfate (DHEA-S), and transvaginal ultrasound with isoechoic image in frosted glass in the left ovary. Left salpingo-oophorectomy was performed, revealing SLCT. Case 2 is a 48-year-old woman with a history of PCOS since the age of 25, prediabetes, and dyslipidemia; she noticed progression of hirsutism, increased libido, deepened voice, alopecia, weight gain, and amenorrhea over the last 5 years. Physical examination revealed hirsutism, alopecia, and clitoromegaly. Tests showed markedly elevated total testosterone (1,080 ng/dl) and normal DHEA-S. Transvaginal ultrasound showed a larger right ovary, without tumor. Ovarian venous sampling showed lateralization towards the right ovary. Bilateral salpingo-oophorectomy plus hysterectomy was performed, revealing SLCT in the right ovary. In both post-surgery patients, there was normalization of androgens and clinical improvement.<br />
<b>Conclusion</b>s: SLCT s can occur at any age, with rapidly evolving hyperandrogenism and/or virilization symptoms, the cases described were of unusual presentation, which posed a diagnostic challenge.