Parikh Pinki, Maheshwari Amita, Rekhi Bharat
Department of Pathology, Tata Memorial Hospital, Parel, Mumbai, Maharashtra, India.
J Cancer Res Ther. 2015 Jul-Sep;11(3):654. doi: 10.4103/0973-1482.140984.
Uterine leiomyosarcomas uncommonly arise on a background of leiomyomas. Still rare is osteosarcomatous dedifferentiation in such tumors. A 60-year-old female presented with abdominal pain and underwent radiological imaging that disclosed a large, well-defined, heterogeneously enhancing uterine tumor. She underwent total abdominal hysterectomy with bilateral salpingectomy. Another, 38-year-old female with the complaints of infertility underwent myomectomy for multiple fibroids. Multiple tumor sections from both the cases showed leiomyomas along with leiomyosarcomas and osteosarcomatous dedifferentiation. Immunohistochemically, both the tumors displayed diffuse expression of smooth muscle markers in areas of leiomyomas, reduced expression of the same in areas of leiomyosarcoma and absent expression in areas of osteosarcomatous dedifferentiation. Unfortunately, both the cases were lost to follow-up. Present cases constitute as rare documentations of uterine leiomyosarcomas, arising on a background of leiomyomas and exhibiting osteosarcomatous dedifferentiation. The value of identifying these tumor components, with extensive tumor sampling relates to their relatively aggressive clinical course.
子宫平滑肌肉瘤很少在平滑肌瘤的基础上发生。这种肿瘤中骨肉瘤样去分化仍然罕见。一名60岁女性因腹痛就诊,影像学检查发现一个大的、边界清晰、强化不均匀的子宫肿瘤。她接受了全腹子宫切除术及双侧输卵管切除术。另一名38岁女性因不孕主诉接受了多发性肌瘤切除术。两例的多个肿瘤切片均显示平滑肌瘤伴平滑肌肉瘤及骨肉瘤样去分化。免疫组化显示,两例肿瘤在平滑肌瘤区域均弥漫性表达平滑肌标志物,在平滑肌肉瘤区域表达减少,在骨肉瘤样去分化区域无表达。不幸的是,两例均失访。目前的病例是子宫平滑肌肉瘤罕见的记录,发生于平滑肌瘤背景并表现出骨肉瘤样去分化。通过广泛的肿瘤取样识别这些肿瘤成分的价值与其相对侵袭性的临床病程有关。