Lipoleiomyosarcoma of the uterus: A case report and review.
10.5468/kjog.2010.53.11.1019
- Author:
Eun Ju HWANG
1
;
Myong Cheol LIM
;
Eun Na KIM
;
Youngmee KWON
;
Eun Kyung HONG
;
Dae Chul JUNG
;
Sang Yoon PARK
Author Information
1. Center for Uterine Cancer, Research Institute and Hospital, National Cancer Center, Goyang, Korea. sypark.ncc@hotmail.com
- Publication Type:Case Report
- Keywords:
Leiomyosarcoma;
Liposarcoma;
Lipoleiomyosarcoma;
Uterus
- MeSH:
Biopsy;
Female;
Follow-Up Studies;
Humans;
Hysterectomy;
Leiomyosarcoma;
Liposarcoma;
Lymph Node Excision;
Lymph Nodes;
Magnetic Resonance Imaging;
Metrorrhagia;
Middle Aged;
Neoplasm Metastasis;
Pelvis;
Sarcoma;
Uterus
- From:Korean Journal of Obstetrics and Gynecology
2010;53(11):1019-1023
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Heterologous sarcomas of the uterus are rare neoplasms. We report a rare case of heterologous uterine sarcoma composed of leiomyosarcomatous and liposarcomatous components with a brief review of literature. A 53-year-old woman had vaginal spotting. The endometrial biopsy performed at a local clinic revealed a high grade spindle cell sarcoma. Pelvis magnetic resonance imaging showed about 5.4 cm sized multiseptated T1 and T2 high signal mass in a uterine fundus without lymph node metastasis or pelvic wall involvement. Total laparoscopic hysterectomy, bilateral salpingo-oophorectomy, pelvic and para-aortic lymph node dissection, and peritoneal washing cytology were performed. Pathologic diagnosis was made as leiomyosarcoma with liposarcomatous differentiation (lipoleiomyosarcoma). The patient received adjuvant postoperative radiotherapy (5040 cGy). Follow up images showed no evidence of disease 8 months after surgery.
