Flint Matthew, Velasquez Jessica, Carr Caitlin, Kolev Valentin, Zakashansky Konstantin
Department of Obstetrics, Gynecology, and Reproductive Science, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Department of Obstetrics, Gynecology, and Reproductive Science, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Int J Surg Case Rep. 2023 Mar;104:107937. doi: 10.1016/j.ijscr.2023.107937. Epub 2023 Feb 17.
Ovarian carcinosarcomas (OCS) are highly aggressive tumors containing both carcinomatous and sarcomatous elements. Patients are typically older postmenopausal women who present with advanced disease, however rarely young women can be affected.
A 41-year-old woman undergoing fertility treatment was found to have a new 9-10 cm pelvic mass on routine transvaginal ultrasound (TVUS) 16 days after embryo transfer. Diagnostic laparoscopy revealed a mass in the posterior cul-de-sac that was surgically excised and sent to pathology for evaluation. Pathology was consistent with carcinosarcoma of gynecologic origin. Further work-up revealed advanced disease with apparent rapid progression. Patient underwent interval debulking surgery after four cycles of neoadjuvant chemotherapy with carboplatin and paclitaxel with final pathology consistent with primary ovarian carcinosarcoma and complete gross resection of disease.
In the setting of advanced disease neoadjuvant chemotherapy with a platinum-based chemotherapy regimen followed by cytoreductive surgery is a standard approach to treatment of OCS. Given the rarity of disease, most data regarding treatment has been extrapolated from other forms of epithelial ovarian cancer. Specific risk factors for disease development of OCS including the long-term effects of assisted reproductive technology remain understudied.
While OCS are rare highly aggressive biphasic tumors that primarily affect older postmenopausal woman, we present a unique case of OCS incidentally found in a young woman undergoing fertility treatment via in-vitro fertilization.
卵巢癌肉瘤(OCS)是极具侵袭性的肿瘤,包含癌性和肉瘤性成分。患者通常为绝经后老年女性,表现为晚期疾病,然而年轻女性也可能极少受到影响。
一名41岁接受生育治疗的女性在胚胎移植16天后经常规经阴道超声(TVUS)检查发现盆腔有一个新的9 - 10厘米肿块。诊断性腹腔镜检查发现后穹窿有一个肿块,手术切除后送病理检查评估。病理结果与妇科来源的癌肉瘤一致。进一步检查显示疾病已进展至晚期且进展明显迅速。患者在接受四个周期的卡铂和紫杉醇新辅助化疗后接受了间隔减瘤手术,最终病理结果与原发性卵巢癌肉瘤一致,且疾病实现了完全肉眼切除。
对于晚期疾病,采用铂类化疗方案进行新辅助化疗,随后进行细胞减灭术是治疗OCS的标准方法。鉴于该疾病罕见,大多数关于治疗的数据是从其他形式的上皮性卵巢癌推断而来的。OCS疾病发展的特定风险因素,包括辅助生殖技术的长期影响,仍未得到充分研究。
虽然OCS是罕见的、极具侵袭性的双相肿瘤,主要影响绝经后老年女性,但我们报告了一例在接受体外受精生育治疗的年轻女性中偶然发现的OCS独特病例。