Ovarian Sertoli Cell Tumor Coexisting With Uterine Malformation: A Case Report.
Ovarian Sertoli cell tumors (SCTs) are a rare subgroup of gonadal ovarian neoplasms. They typically occur in young patients and are usually benign. We present a case report of an elderly patient with uterine maldevelopment in whom a gigantic ovarian SCT was diagnosed.
A 62-year-old woman presented to the emergency department for treatment of a lower limb infection. She additionally reported abdominal girth, loss of appetite, and a sensation of epigastric fullness. Physical examination revealed an abdominal mass. Imaging showed a massive tumor measuring approximately 19.0×12.0×19.0 cm. Initial differential diagnosis included uterine fibroid or ovarian teratoma. Laparotomy was performed, during which a normal uterus was not identified. The excised tumor had a smooth capsule, a solid lobulated structure, and a grayish-yellow color with fine calcifications. Peritoneal fluid obtained at surgery contained no malignant cells. Follow-up at 16 months showed no clinical or radiological evidence of recurrence. The patient's follow-up is ongoing.
This case underscores the importance of including rare ovarian tumors in the differential diagnosis of pelvic masses, particularly in patients with congenital reproductive tract anomalies.
A 62-year-old woman presented to the emergency department for treatment of a lower limb infection. She additionally reported abdominal girth, loss of appetite, and a sensation of epigastric fullness. Physical examination revealed an abdominal mass. Imaging showed a massive tumor measuring approximately 19.0×12.0×19.0 cm. Initial differential diagnosis included uterine fibroid or ovarian teratoma. Laparotomy was performed, during which a normal uterus was not identified. The excised tumor had a smooth capsule, a solid lobulated structure, and a grayish-yellow color with fine calcifications. Peritoneal fluid obtained at surgery contained no malignant cells. Follow-up at 16 months showed no clinical or radiological evidence of recurrence. The patient's follow-up is ongoing.
This case underscores the importance of including rare ovarian tumors in the differential diagnosis of pelvic masses, particularly in patients with congenital reproductive tract anomalies.
Authors
BiegaĆska BiegaĆska, Biczak Biczak, Przywara Przywara, Blok Blok, FuĆawka FuĆawka, HaĆoĆ HaĆoĆ, Murawski Murawski
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