Título: Dysgerminoma complicating Swyer Syndrome: A case report
Autores: Secilmis Kerimoglu, Ozlem; Selcuk University
Fecha: 2013-09-23
Publicador: International Journal of Mevlana Medical Sciences
Fuente:
Tipo: info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion

Tema: Swyer syndrome, Dysgerminoma, Amennorhea
Descripción: Swyer syndrome is a kind of gonadal dysgenesis characterized by a female phenotype and 46 XY karyotype. Bilateral dysgenetic gonads have a high potential for malignancy. A 16-years-old female was presented to our hospital with  primary amenorrhea. Pelvic ultrasound revealed a 6 cm solid mass in the right adnexal area. In genetic analysis, the patient’s karyotype was 46 XY. She underwent laparatomy. Upon the result of frozen section evaluation of gonad that showed dysgerminoma, pelvic lymphadenectomy and omentectomy were performed. She was considered to be stage 3C and received chemotherapy with bleomycin-cisplatin-etoposide. Due to high risk for tumor, gonadectomy should be performed immediately after the diagnosis.
Idioma: Inglés

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