Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/9945
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dc.contributor.authorMensah, Samuel-
dc.contributor.authorKyei, Ishmael-
dc.contributor.authorOhene –Yeboah, Michael-
dc.contributor.authorAdjei, Ernest-
dc.date.accessioned2023-10-24T11:12:04Z-
dc.date.available2023-10-24T11:12:04Z-
dc.date.issued2016-
dc.identifier.urihttp://hdl.handle.net/123456789/9945-
dc.description.abstractSclerosing stromal tumour (SST) is a rare benign sex cord stromal tumour of the ovary. We report a case of sclerosing stromal tumour of the mesentery in a 32-year-old Para one who presented with intra abdominal mass, menstrual irregularity and secondary infertility. Histopathology and immunohistochemistry of the completely excised tumour was consistent with sclerosing stromal tumour, immunoreactive only to vimentin. No ovarian tissue was found in the sectioned tumour. Her menses became regular and she conceived 3 months after complete excision and delivered after 9 months. Hormonal assay was not done because SST was least suspected. From literature this is the first case of SST in the transverse mesocolon reported in the West African subregion, and may probably be one of the rare cases of hormonally active SST.en_US
dc.language.isoenen_US
dc.subjectExtragonadalen_US
dc.subjectsclerosing stromal tumouren_US
dc.subjectHormonally activeen_US
dc.subjectsecondary infertilityen_US
dc.subjectGhanaen_US
dc.titleExtra gonadal sclerosing stromal tumour in the transverse mesocolonen_US
dc.typeArticleen_US
Appears in Collections:School of Medical Sciences

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