Literature DB >> 3692675

Uterine intravascular leiomyomatosis: an update and report of seven cases.

F F Nogales1, N Navarro, J M Martinez de Victoria, F Contreras, C Redondo, M A Herraiz, M A Seco, A Velasco.   

Abstract

A clinicopathological study of seven cases of intravascular leiomyomatosis (IVL) was performed. The patients' ages ranged from 29 to 80 and all cases were associated with uterine leiomyomas. The intravascular extension involved preferentially uterine vessels, although the adnexa were also affected. Microscopically, the intravascular tumors resembled the primary leiomyomas. Mitotic count was low and never exceeded 3 per 10 high-power fields. Thick venous vessels, sometimes with thrombosis, were a conspicuous marker in intravascular locations. Necrosis and hemorrhage were found in four cases. Epithelioid IVL was found in one instance associated with a lipid cell tumor of the ovary. This series supports, for most cases, the notion of an origin from a preexisting leiomyoma. A review of treatment, prognosis, and histogenesis of IVL is performed.

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Year:  1987        PMID: 3692675

Source DB:  PubMed          Journal:  Int J Gynecol Pathol        ISSN: 0277-1691            Impact factor:   2.762


  1 in total

1.  Case report 720. Multicentric mixed tumor of bone with pulmonary involvement.

Authors:  A G Rose; N G Heselson; R K Marks; D Kranold
Journal:  Skeletal Radiol       Date:  1992       Impact factor: 2.199

  1 in total

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