A huge retroperitoneal liposarcoma mimicking ovarian teratoma: A case report

U. Jahan, Neena Gupta, Rashmi Yadav, Noor Fatima
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Abstract

Retroperitoneal liposarcoma is a malignant, primitive, and rare mesenchymal tumor. It can grow usually asymptomatic until large enough to compress the surrounding organs. We report an observation of a retroperitoneal liposarcoma mimicking an ovarian tumor. A 50-year-old, P1+0 postmenopausal female, presented to our Department of Obstetrics and Gynecology, with abdominopelvic mass and pressure symptoms for 2 months. Her magnetic resonance imaging abdomen and pelvis, ULTRASOUND-guided fine needle aspiration cytology, and tumor markers were done to make the provisional diagnosis after which, the patient underwent exploratory laparotomy. Complete removal of mass along with the right ovary was done in spite of mass encasing the right iliac vessels and the right ureter. Along with this, a hysterectomy with the left salpingo-oophorectomy and the right salpingectomy were done. A very huge ovarian tumor 22×15×28 cm weighing 5.5 kg was removed. Histopathological examination showed myxoid/well-differentiated liposarcoma with heterologous differentiation. Retroperitoneal liposarcomas are rare; however, they require an aggressive surgical approach, including multi-organ resection, if necessary, or multiple resections in the case of recurrence.
模仿卵巢畸胎瘤的巨大腹膜后脂肪肉瘤:病例报告
腹膜后脂肪肉瘤是一种恶性、原始和罕见的间质肿瘤。它通常无症状生长,直到大到足以压迫周围器官。我们报告了一起模仿卵巢肿瘤的腹膜后脂肪肉瘤病例。一名 50 岁、绝经后 P1+0 的女性因腹部盆腔肿块和压迫症状 2 个月来我院妇产科就诊。经过腹部和盆腔磁共振成像、超声引导下细针穿刺细胞学检查和肿瘤标记物检查后,患者接受了剖腹探查术。尽管肿块包裹着右侧髂血管和右侧输尿管,但还是将肿块和右侧卵巢完全切除。同时还进行了子宫切除术,包括左侧输卵管切除术和右侧输卵管切除术。切除了一个 22×15×28 厘米、重 5.5 公斤的巨大卵巢肿瘤。组织病理学检查显示为肌样/分化良好的脂肪肉瘤,伴有异源分化。腹膜后脂肪肉瘤非常罕见,但需要采取积极的手术方法,包括必要时切除多个器官,或在复发的情况下进行多次切除。
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