Jabri Hatim, Balde Fatoumata Binta, Mahmoud Mohammed, Alaoui Othmane, Mahmoudi Abdelhalim, Khatalla Khalid, Bouabdallah Youssef
Pediatric Surgery, Hassan II Hospital of Fez, Sidi Mohamed Ben Abdellah University, Faculty of Medicine and Pharmacy of Fez, Fez, MAR.
Cureus. 2024 Jul 1;16(7):e63554. doi: 10.7759/cureus.63554. eCollection 2024 Jul.
Ovarian Sertoli-Leydig cell tumors (SLCT) are extremely rare malignant tumors deriving from the sex cord stroma. An abdominal mass and a virilization syndrome dominate the clinical symptoms. This particular tumor poses diagnostic and therapeutic problems. Prognosis depends on staging (the International Federation of Gynecology and Obstetrics (FIGO)/tumor, node, metastasis (TNM)) and differentiation. The treatment is surgical, combined with adjuvant chemotherapy in certain cases. We report the case of a three-year-old girl admitted to our department for signs of virilization with an abdominal mass. The literature does not contain any reports of a younger case. Ovarian SLCTs should be considered in every girl presenting with signs of virilization and a lower abdominal mass. The prognosis and management depend on the results of the histological analysis and extension evaluation in order to define therapeutic management.
卵巢支持-间质细胞瘤(SLCT)是一种极为罕见的源自性索间质的恶性肿瘤。腹部肿块和男性化综合征是其主要临床症状。这种特殊的肿瘤带来了诊断和治疗方面的问题。预后取决于分期(国际妇产科联盟(FIGO)/肿瘤、淋巴结、转移(TNM))和分化程度。治疗以手术为主,某些情况下联合辅助化疗。我们报告了一名3岁女童因男性化体征和腹部肿块入住我科的病例。文献中尚无更年幼病例的报道。对于每一位出现男性化体征和下腹部肿块的女童,都应考虑卵巢SLCT的可能。预后和治疗管理取决于组织学分析结果和扩展评估,以便确定治疗方案。