Sertoli-Leydig tumor in a 17-year-old girl: a case report
DOI:
https://doi.org/10.18203/2320-1770.ijrcog20241085Keywords:
Case report, Tumor, Sertoli-Leydig, Ovary, HaitiAbstract
Sertoli-Leydig tumors of the ovary are rare. They can affect women in all age groups but are more frequent in the first three decades. No case of Sertoli-Leydig cells tumors has been reported in the Haitian literature. We present a case of a 17-year-old teenage who was seen in the outpatient clinic of the Mirebalais teaching hospital for: amenorrhea, change in voice and hair loss. After our evaluation and the completion of certain assessments, the clinical impression of a stromal and sexual cord tumor was retained, which guided us to perform a laparotomy. We conclude that in the management of this type of case, it is important to take into account the desire to preserve the patient's subsequent fertility and if there is one point that should not be overlooked, it is the psychosocial repercussions of the pathology before and after its treatment.
Metrics
References
Moussa D, Aziz DA, Niassy DAC, Espérence KC, Youssou N, Charles MJ, et al. Sertoli-leydig cell tumor of the ovary: report of a case in a 22-year-old girl. Pan Afr Med J. 2016;25:2-5.
Castro BGR, De Pádua Souza C, Da Cunha Andrade CEM, De Andrade Vieira M, De Andrade DAP, Dos Reis R. Ovarian Sertoli-Leydig Cell Tumors: Epidemiological, Clinical and Prognostic Factors. Revista Brasileira de Ginecologia e Obstetricia. 2019;41(7):440-8.
Akman L, Ertas IE, Gokcu M, Terek MC, Sanci M, Sanli U, et al. Ovarian sertoli-leydig cell tumors: A multicenter long-term clinicopathological analysis of 27 patients. J Cancer Res Therapeutics. 2016;12(1):290-94.
Chen L, Tunnell CD, De Petris GD. Sertoli-Leydig cell tumor with heterologous element: A case report and a review of the literature. Int J Clin Experiment Pathol. 2014;7(3):1176-81.
Xu Q, Zou Y, Zhang XF. Sertoli-Leydig cell tumors of ovary. Medicine. 2018;97:42(e12865).
Lantzsch T, Stoerer S, Lawrenz K, Buchmann J, Strauss HG, Koelbl H. Sertoli-Leydig cell tumor. Arch Gynecol Obstetr. 2001;264(4):206-8.
Samal S, Chimote A, Juneja R, Agrawal M. Sertoli-Leydig cell tumor (arrhenoblastoma) in adolescent age group. Int J Reproduct Contracept Obstetr Gynecol. 2013;2(4):722.
Juniarto AZ, Setiawati BA, Ediati A, van der Zwan YG, Looijenga LHJ, De Jong FH, et al. Virilization due to androgen hypersecretion in a patient with ovarian leydig cell tumor: diagnostic and psychosocial implications. Acta Medica Indonesiana. 2013;45(2):130-5.
Fahim E, Alexander K, Mirjam C-C, ¬Emanuel C. Hirsutism, complexity of differential diagnosis and treatment, Swiss Medical Forum. 2018;18(47):981-8.
De Oliveira Franzin CM, Kraft ML, Faundes D, Zeferino LC, Alvarenga M, Marussi EF. Detection of ovarian Sertoli-Leydig cell tumors exclusively by color Doppler sonography. J Ultrasound Med. 2006;25(10):1327-30.
Abu-Zaid A, Azzam A, Alghuneim LA, Metawee MT, Amin T, Al-Hussain TO. Poorly Differentiated Ovarian Sertoli-Leydig Cell Tumor in a 16-Year-Old Single Woman: A Case Report and Literature Review. Case Rep Obstetr Gynecol. 2013;1-6.
Naphtho I, Fedorov NV, Anisimov AV, Viktorova EA. Ovarian Sertoli-Leydig Cell tumour with α-fetoprotein- produCing intestinal glandular Cells. Clin Case Short Rev basic Lit. 1989;70(12):1356-9.