Barel Oshri, Qian Christine, Manolitsas Tom
Monash Medical Centre Department of Obstetrics and Gynecology, Clayton, Victoria, Australia; Asaf Harofe Medical Center Zeriffin, Department of Obstetrics and Gynecology, Tel Aviv University Faculty of Medicine, Tel Aviv, Israel.
Cabrini Hospital, Malvern, Victoria, Australia.
Gynecol Oncol Rep. 2016 Jul 7;17:75-8. doi: 10.1016/j.gore.2016.07.002. eCollection 2016 Aug.
Primary omental leiomyosarcoma is a rare tumor. We report a case of successfully resected omental leiomyosarcoma whose presentation mimicked ovarian carcinoma. Symptoms of abdominal distension and discomfort that lasted 8 months followed by pain lead to a diagnosis of a large mass in the abdomen. Physical examination revealed a large, over 20 cm tumor, suspected to be of ovarian origin. A small amount of ascites was found on Computerized Tomography (CT) and ultrasound (US) scans. Total abdominal hysterectomy with bilateral salpingo-oophorectomy, omentectomy and tumor debulking procedure was planned. Laparotomy revealed normal uterus ovaries and tubes with a leiomyosarcoma of the omentum which was completely resected successfully. Only 26 cases of primary leiomyosarcoma of the omentum were previously described in the literature. A review of the literature is also presented.
原发性大网膜平滑肌肉瘤是一种罕见的肿瘤。我们报告一例成功切除的大网膜平滑肌肉瘤病例,其临床表现酷似卵巢癌。持续8个月的腹胀和不适症状随后出现疼痛,导致诊断为腹部有一个大肿块。体格检查发现一个超过20厘米的大肿瘤,怀疑起源于卵巢。计算机断层扫描(CT)和超声(US)检查发现少量腹水。计划进行全腹子宫切除术、双侧输卵管卵巢切除术、大网膜切除术和肿瘤减瘤手术。剖腹手术显示子宫、卵巢和输卵管正常,大网膜有平滑肌肉瘤,已成功完全切除。文献中此前仅描述了26例原发性大网膜平滑肌肉瘤病例。本文还对相关文献进行了综述。