On the pathogenesis of sclerosing stromal tumor of the ovary: A neoplasm in transition

Lawrence M. Roth, Arthur R. Gaba, Liang Cheng

Research output: Contribution to journalArticle

4 Scopus citations

Abstract

Sclerosing stromal tumor (SST) is a distinctive benign ovarian stromal neoplasm first reported in 1973. Although its initial description supports its characterization as an ovarian stromal tumor, its exact pathogenesis remains uncertain. It is usually hormonally inactive, but occasional tumors are estrogenic or androgenic, and virilization can occur during pregnancy. We report 11 cases of SST, 6 of which were associated with another type or other types of ovarian stromal tumor. In 4 of these, a transition from thecoma of either typical or luteinized type to SST was observed. Our index case was that of a 16-yr-old girl who had a typical thecoma that underwent involutional changes in an extensive subserosal portion of the tumor with conversion to SST. In our series, 3 cases of SST underwent transformation to ovarian myxoma, one of which also contained a component of thecoma. The active SST components stained for inhibin, steroidogenic factor 1, and α-smooth muscle actin, but were negative or occasionally weakly positive for desmin.

Original languageEnglish (US)
Pages (from-to)449-462
Number of pages14
JournalInternational Journal of Gynecological Pathology
Volume33
Issue number5
DOIs
StatePublished - Sep 2014

Keywords

  • Juvenile-type granulosa cell tumor
  • Ovarian stromal tumor
  • Ovary
  • Sclerosing stromal tumor
  • Thecoma

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Obstetrics and Gynecology
  • Medicine(all)

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