2020
DOI: 10.18203/2320-6012.ijrms20201358
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Ovarian fibrothecoma with minor sex cord elements: a case report

Abstract: Ovarian fibroma is the most common sex cord stromal tumour of ovary accounting to 1-5% of all ovarian tumours. Minor sex cord elements in ovarian fibroma are a rare entity occupying less than 10% of tumour area. To the best of our knowledge only 20 cases has been reported till date. This case is presented because of its rarity. Authors reported a case of fibrothecoma with minor sex cord elements in a 70yr old postmenopausal women who presented with postmenopausal bleeding with abdominal mass.

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Cited by 2 publications
(5 citation statements)
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“…Macroscopically, ovarian fibromas are firm, white masses with smooth lobulated appearance, sometimes cystic degeneration or stromal edema is also noted. This generally resembles a uterine leiomyoma [9] . Microscopically, intersecting bundles of spindle cells producing collagen are seen.…”
Section: Discussionmentioning
confidence: 95%
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“…Macroscopically, ovarian fibromas are firm, white masses with smooth lobulated appearance, sometimes cystic degeneration or stromal edema is also noted. This generally resembles a uterine leiomyoma [9] . Microscopically, intersecting bundles of spindle cells producing collagen are seen.…”
Section: Discussionmentioning
confidence: 95%
“…Surgery is the mainstay of treatment which can be performed by laparotomy or laparoscopically. Salpingo-ovariotomy should be performed in perimenopausal or postmenopausal women while cystectomy should be considered in younger patients [9] . In our case, conservation of the ovary was not possible as no ovarian tissue could be separated from the large solid mass and there was high index of suspicion for malignancy.…”
Section: Discussionmentioning
confidence: 99%
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“…It was first described by Young and Scully in 1983 as a predominantly fibromatous or thecomatous tumor, with minor sex cord elements occupying <10% of the tumor area [1]. To the best of our knowledge, only 20 cases have been reported [1][2][3][4][5][6], and no detailed imaging findings are available. Here, we present magnetic resonance imaging (MRI) findings of this rare tumor.…”
Section: Introductionmentioning
confidence: 99%