| Literature DB >> 2722175 |
R J Brescia1, H D Tazelaar, J Hobbs, A W Miller.
Abstract
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.Entities:
Mesh:
Year: 1989 PMID: 2722175 DOI: 10.1016/0046-8177(89)90132-9
Source DB: PubMed Journal: Hum Pathol ISSN: 0046-8177 Impact factor: 3.466