@article{Tarenia_Chattopadhyay_Niladri Das_Hathi_Baidya_Chakrabarty_Sengupta_Goswami_2022, title={Swyer Syndrome Presenting as Dysgerminoma: A Case Report}, volume={38}, url={https://www.asean-endocrinejournal.org/index.php/JAFES/article/view/2159}, DOI={10.15605/jafes.038.01.15}, abstractNote={<p>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.</p>}, number={1}, journal={Journal of the ASEAN Federation of Endocrine Societies}, author={Tarenia, Silima and Chattopadhyay, Sujaya and Niladri Das and Hathi, Deep and Baidya, Arjun and Chakrabarty, Puranjoy and Sengupta, Nilanjan and Goswami, Soumik}, year={2022}, month={Nov.}, pages={108–113} }