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Thecoma is a rare type of ovarian sex cord-stromal tumor, accounting for about 0.5% to 1.0% of ovarian tumors. This tumor mainly occurs in women before and after menopause and is relatively rare before puberty. Thecoma generally consists of benign solid or cystic masses and can be accompanied by ascites, abnormal hormone levels, and elevated CA125. Most of these tumors have a good prognosis. In this case study, we report on a 16-year-old girl who presented with bloating and a huge abdominal mass. A full-body computed tomography (CT) showed a huge cystic mass in the pelvic and abdominal cavities indicative of malignancy. The abdominal ultrasound (US) showed a huge solid hypoechoic mass reaching up to the lower abdomen and pelvic cavities. The tumor markers and estradiol were within the normal range. The tumor was surgically removed, and the histopathological examination revealed a solid thecoma measuring about 26 cm × 20 cm × 12 cm. Although thecomas mostly occur in perimenopausal and postmenopausal women, the findings of this case study suggest that thecomas should not be ruled out in adolescents presenting with a large pelvic mass. Abdominal US could be used to facilitate the differentiation between fluid-filled and solid masses, which can be difficult to distinguish on a CT scan.
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http://dx.doi.org/10.1186/s12905-025-03820-1 | DOI Listing |
BMC Womens Health
July 2025
Center of Obstetrics and Gynecology, Peking University Shenzhen Hospital, Shenzhen, 518036, P. R. China.
Thecoma is a rare type of ovarian sex cord-stromal tumor, accounting for about 0.5% to 1.0% of ovarian tumors.
View Article and Find Full Text PDFJ Pediatr Adolesc Gynecol
October 2016
Department of Obstetrics and Gynecology, Aichi Medical University School of Medicine, Nagakute, Aichi, Japan.
Background: Meigs syndrome is a rare complication associated with ovarian fibromas. Although ovarian fibromas are rare in children, they are common in women with Gorlin syndrome after puberty.
Case: A 14-year-old girl with Gorlin syndrome was admitted to our hospital for ablation of basal cell carcinoma.
J Obstet Gynaecol India
October 2011
Department of Obstetrics and Gynecology, University College of Medical Sciences & Guru Teg Bahadur Hospital, G-367, Preet Vihar, Delhi, 110092 India.
Objectives: The sex cord stromal tumors (SCST) account for approximately 7% of all malignant ovarian tumors. They are endocrinologically active tumors of which granulosa cell tumors are the commonest. We describe an analysis of all cases of SCST managed, in our department over the last five years and discuss two cases of unusual presentation of these tumors.
View Article and Find Full Text PDFJ Pediatr Adolesc Gynecol
August 2010
Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
Background: The differential diagnosis for precocious puberty in a young female includes peripheral causes. This case documents a rare cause of peripheral precocious puberty--a juvenile granulosa and theca cell ovarian tumor--and a brief review of the literature for this tumor type.
Case: A 7-year-old girl presented with rapid onset of pubertal development and elevated estradiol levels.
Med Pregl
October 1999
Sluzba za zdravstvenu zastitu zena, Zdravstveni centar Dr Gere Istvan, Senta.
Introduction: Authors have investigated the incidence and distribution of hormonally active ovarian tumors in a 30-year surgical material. Out of 552 ovarian tumors, there were 28 hormonally active tumors (5.07%): 18 granulosa cell tumors, 4 thecomas, 2 arrhenoblastomas, 2 malignant v.
View Article and Find Full Text PDF