Sclerosing stromal tumor: a rare ovarian neoplasm

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dc.contributor.authorKadirogullari, Pinar
dc.contributor.authorSeckin, Kerem Doga
dc.date.accessioned2023-02-21T12:33:27Z
dc.date.available2023-02-21T12:33:27Z
dc.date.issued2022-01-01
dc.description.abstractSclerosing stromal tumor (SST) is an extremely rare and distinctive sex cord stromal tumor, which occurs predominantly in the second and third decades of life. SSTs make up 2-6\% of ovarian sex-cord stromal tumors. Due to the solid and distinct vascular structure of the tumor, it can be mistaken as a number of malignant ovarian tumors. As this specific neoplasm is very rare, it is not always possible to diagnose the tumor preoperatively with clinical and ultrasonographic findings. Furthermore, histopathological and immunohistochemical analysis does not always confirm the diagnosis. In this case report, clinical findings, histopathological features, and macroscopic appearance during laparoscopy of an SST are presented in a 20-year-old woman with pelvic pain. SST should be considered among the differential diagnosis of women with adnexal masses.
dc.description.issue1
dc.description.issueMAR
dc.description.pages68-70
dc.description.volume23
dc.identifier.doi10.4274/jtgga.galenos.2021.2021.0097
dc.identifier.urihttps://hdl.handle.net/11443/1492
dc.identifier.urihttp://dx.doi.org/10.4274/jtgga.galenos.2021.2021.0097
dc.identifier.wosWOS:000848663800013
dc.publisherGALENOS PUBL HOUSE
dc.relation.ispartofJOURNAL OF THE TURKISH-GERMAN GYNECOLOGICAL ASSOCIATION
dc.subjectBenign ovarian neoplasm
dc.subjectlaparoscopy
dc.subjectsclerosing stromal tumor
dc.titleSclerosing stromal tumor: a rare ovarian neoplasm
dc.typeArticle
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