Swyer Syndrome Presenting as Dysgerminoma
A Case Report
DOI:
https://doi.org/10.15605/jafes.038.01.15Keywords:
Swyer syndrome, dysgerminoma, amenorrhoea, gonadal dysgenesisAbstract
Complete gonadal dysgenesis with 46,XY karyotype is a clinical condition characterized by the absence of testicular tissue but typical Mullerian structures in a phenotypically female individual. The condition presents as primary amenorrhoea or delayed puberty. Eventually, malignant neoplasms may arise. We report a case of a 16-year-old patient with Swyer syndrome presenting with primary amenorrhoea and with previous diagnosis four years earlier of a malignant dysgerminoma in the right ovary.
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