Abstract
Introduction. Ovarian carcinosarcoma (OCS), also known as malignant mixed Müllerian tumour (MMMT), is one of the rarest histological subtypes of ovarian cancer. It is an aggressive tumour with a dismal prognosis—the median survival of patients is less than two years. The rarity of the disease generates many controversies about histogenesis, prognostic factors and treatment of OCS. Histologically, OCS is composed of an epithelial and sarcomatous component. Case report. In the present case, a patient with bilateral ovarian cysts and bulky paraaortic lymph nodes is reported. Retroperitoneal paraaortic lymph node metastases were the only extrapelvic dissemination of OCS. The patient underwent comprehensive surgical staging procedures, including total abdominal hysterectomy and bilateral salpingo-oophorectomy, supracolic omentectomy and selective para-aortic lymphadenectomy. Histologically the ovarian carcinosarcoma was composed of an epithelial component (high-grade serous adenocarcinoma) and three sarcomatous components (homologous—endometrial stromal cell sarcoma, and heterologous—chondrosarcoma, rhabdomyosarcoma). Immunohistochemistry staining was performed. A postoperative complication (adhesion between the abdominal aorta and terminal ileum causing obstructive ileus) that has never been reported in the medical literature occurred. Conclusion. Carcinosarcomas are carcinomas with epithelial–mesenchymal transition and heterologous differentiation. Retroperitoneal pelvic and paraaortic lymph nodes should be carefully inspected in patients with ovarian tumours. Adhesions between the small bowels and abdominal aorta are possible complications after lymph node dissection in the paraaortic region.
Highlights
IntroductionOvarian cancer is the fifth most common cause of cancer death among women, and ninety percent of ovarian cancers are of an epithelial cell type, while sex cord-stromal tumours and malignant ovarian germ cell tumours are relatively rare [1]
Ovarian carcinosarcoma (OCS), known as malignant mixed Müllerian tumour (MMMT), is one of the rarest histological subtypes of ovarian cancer
Yalcin et al compared the prognosis of patients with OCS to patients with ovarian high-grade serous carcinoma treated in the same manner: optimal cytoreductive surgery followed by platinum plus taxane combination chemotherapy
Summary
Ovarian cancer is the fifth most common cause of cancer death among women, and ninety percent of ovarian cancers are of an epithelial cell type, while sex cord-stromal tumours and malignant ovarian germ cell tumours are relatively rare [1]. Ovarian carcinosarcoma (OCS), known as malignant mixed Müllerian tumour (MMMT), is one of the rarest histological subtypes of ovarian cancer. OCS represents 1–4% of all ovarian tumours [2,3]. OCS is composed of an epithelial and sarcomatous component—homologous (i.e., having Müllerian pathology) and heterologous [2,4]. In the current case study, a case of a female patient with bilateral ovarian OCS treated with optimal cytoreductive surgery is reported. An ethical committee approval (number 546 /30.10.2019) was obtained for it
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