Yamaguchi Maiko, Kusunoki Soshi, Hirayama Takashi, Fujino Kazunari, Terao Yasuhisa, Itakura Atsuo
Department of Obstetrics and Gynecology, Juntendo University Faculty of Medicine, Tokyo, Japan.
J Obstet Gynaecol Res. 2019 Sep;45(9):1944-1947. doi: 10.1111/jog.14037. Epub 2019 Jun 19.
Uterine leiomyosarcoma (LMS) is a rare tumor. It has not been established if these tumors arise de novo or from pre-existing leiomyomas (LM). We report a case herein of LMS arising from a subserosal LM. A 47-year-old nulliparous woman was diagnosed with a uterine tumor measuring 30 cm in diameter by pelvic magnetic resonance imaging. Serum CA-125 level was 369 U/mL, and the lactate dehydrogenase level was elevated (565 IU/L, respectively). Positron emission tomography-computed tomography revealed abnormal uptake (SUV = 25.29) of the abdominal tumor. Upon laparotomy, a large tumor with solid and cystic components was shown to arise from a subserosal LM, with invasion into the greater omentum and small intestine. Abdominal hysterectomy, bilateral salpingo-oophorectomy, omentectomy and small intestine resection were performed. Macroscopic findings showed that the LMS was adherent to a subserosal LM, without continuity between the tumor and the uterus. Our case supports the hypothesis that LMS can arise from a pre-existing LM.
子宫平滑肌肉瘤(LMS)是一种罕见肿瘤。这些肿瘤是新发的还是由先前存在的平滑肌瘤(LM)发展而来尚未明确。我们在此报告一例源自浆膜下平滑肌瘤的子宫平滑肌肉瘤病例。一名47岁未生育女性经盆腔磁共振成像诊断为直径30厘米的子宫肿瘤。血清CA - 125水平为369 U/mL,乳酸脱氢酶水平升高(分别为565 IU/L)。正电子发射断层扫描 - 计算机断层扫描显示腹部肿瘤有异常摄取(SUV = 25.29)。剖腹探查时发现一个有实性和囊性成分的大肿瘤源自浆膜下平滑肌瘤,侵犯大网膜和小肠。进行了腹式子宫切除术、双侧输卵管卵巢切除术、大网膜切除术和小肠切除术。宏观检查发现平滑肌肉瘤附着于浆膜下平滑肌瘤,肿瘤与子宫之间无连续性。我们的病例支持子宫平滑肌肉瘤可由先前存在的平滑肌瘤发展而来这一假说。