RESUMEN
Dysgerminoma developed in a 21-year-old phenotypic female patient with 46,XY pure gonadal dysgenesis, Swyer syndrome. This patient presented with pelvic mass associated with abdominal pain and primay amenorrhea. Clinical characteristics showed a typical stigmata of gonadal dysgenesis: primary amenorrhea, sexual infantilism, a small uterus and left streak gonad. A 46,XY karyotype was made by lymphocyte culture. The patient was counseled to undergo operation, chemotherapy and hormon therapy. She underwent bilateral gonadectomy with total hysterectomy, partial omentectomy and multiple pelvic wall random biopsy. Histological examination revealed dysgenetic gonads with dysgerminoma. After surgery, the patient received chemotherapy and also was started on hormone replacement therapy. She is currently alive with no evidence of disease after 19 months from surgery.
Asunto(s)
Femenino , Humanos , Adulto Joven , Dolor Abdominal , Amenorrea , Biopsia , Cristianismo , Quimioterapia , Disgerminoma , Disgenesia Gonadal , Disgenesia Gonadal 46 XY , Gónadas , Terapia de Reemplazo de Hormonas , Histerectomía , Cariotipo , Linfocitos , Infantilismo Sexual , ÚteroRESUMEN
No abstract available.
Asunto(s)
Defectos de la Almohadilla Endocárdica , Cojinetes Endocárdicos , Hernia DiafragmáticaRESUMEN
No abstract available.
Asunto(s)
Femenino , Humanos , Embarazo , Embarazo , Diálisis Peritoneal Ambulatoria Continua , Resultado del Embarazo , Diálisis RenalRESUMEN
No abstract available.