Chang E, Shim S I
Department of Pathology, Catholic University of Korea, Seoul.
J Korean Med Sci. 1998 Oct;13(5):559-62. doi: 10.3346/jkms.1998.13.5.559.
A case report of myxoid leiomyosarcoma of the uterus in a 54-year-old woman is presented as a rare variant of uterine sarcoma. Only 14 cases have been described in the literature. These tumors have a striking myxoid appearance and exhibit highly malignant behavior despite their low mitotic index. Although it is difficult to establish the nature of the neoplastic cells in the myxoid areas, both light microscopical and immunohistochemical characteristics showed features of smooth muscle cells in some of the cellular areas. Our patient had a tumor which arose in association with hyalinized benign leiomyomatous lesion. Like other reported cases of myxoid leiomyosarcoma, the tumor behaved aggressively.
本文报告了一例54岁女性子宫黏液样平滑肌肉瘤病例,该病例为子宫肉瘤的一种罕见变体。文献中仅描述了14例此类病例。这些肿瘤具有显著的黏液样外观,尽管其有丝分裂指数较低,但表现出高度恶性行为。尽管很难确定黏液样区域肿瘤细胞的性质,但在一些细胞区域,光镜和免疫组化特征均显示出平滑肌细胞的特征。我们的患者所患肿瘤与透明变性的良性平滑肌瘤病变相关。与其他报道的黏液样平滑肌肉瘤病例一样,该肿瘤具有侵袭性。