Brescia R J, Tazelaar H D, Hobbs J, Miller A W
Department of Pathology, Rush-Presbyterian-St Luke's Medical Center, Chicago.
Hum Pathol. 1989 Mar;20(3):252-6. doi: 10.1016/0046-8177(89)90132-9.
Two cases of intravascular leiomyomatosis (IVL) with histologic features of a lipoleiomyoma (LPL) are reported. Both tumors arose from preexisting uterine leiomyomata. One tumor was found incidentally in a uterus removed for leiomyomata. The other tumor extended up the inferior vena cava into the right side of the heart and presented as a cardiac mass. Although LPL is considered to be a benign lesion, IVL recurs in approximately 10% of reported cases, and must be distinguished from low-grade endometrial stromal sarcoma and leiomyosarcoma with vascular invasion. The combination of features in these cases lends support to the theory that IVL may arise by intravascular extension of a preexisting leiomyoma.
报告了两例具有脂肪平滑肌瘤(LPL)组织学特征的血管内平滑肌瘤病(IVL)。这两个肿瘤均起源于先前存在的子宫平滑肌瘤。其中一个肿瘤是在因平滑肌瘤而切除的子宫中偶然发现的。另一个肿瘤沿下腔静脉向上延伸至心脏右侧,并表现为心脏肿块。尽管LPL被认为是一种良性病变,但IVL在约10%的报告病例中会复发,并且必须与伴有血管侵犯的低级别子宫内膜间质肉瘤和平滑肌肉瘤相鉴别。这些病例中的特征组合支持了IVL可能由先前存在的平滑肌瘤血管内延伸而产生的理论。