Gonadoblastoma bilateral y disgerminoma asociados en un síndrome de Swyer / Bilateral gonadoblastoma and dysgerminoma associated with Swyer syndrome
Prog. obstet. ginecol. (Ed. impr.)
; 53(6): 237-239, jun. 2010. ilus
Article
in Spanish
| IBECS
| ID: ibc-79621
Responsible library:
ES1.1
Localization: BNCS
RESUMEN
El síndrome de Swyer es una disgenesia gonadal pura caracterizada por fenotipo femenino y cariotipo XY. Las pacientes presentan unas gónadas disgenéticas y no funcionantes. El riesgo de neoplasia gonadal es alto, entre un 25 y un 30%. El gonadoblastoma y el disgerminoma son los tumores más frecuentes. Presentamos un caso de gonadoblastoma bilateral y disgerminoma asociados en una paciente con este síndrome (AU)
ABSTRACT
Swyer syndrome is a pure gonadal dysgenesis with female phenotype and 46 XY karyotype. Affected individuals have dysgenetic and non-functioning gonads. The risk of gonadal neoplasia is high at between 25% and 30%. The most frequently reported malignancies are gonadoblastoma and disgerminoma. We report a case of bilateral gonadoblastoma and dysgerminoma in a female patient with this syndrome (AU)
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Collection:
National databases
/
Spain
Database:
IBECS
Main subject:
Gonadoblastoma
/
Dysgerminoma
/
Gonadal Dysgenesis, 46,XY
Type of study:
Risk factors
Limits:
Adolescent
/
Female
/
Humans
Language:
Spanish
Journal:
Prog. obstet. ginecol. (Ed. impr.)
Year:
2010
Document type:
Article
Institution/Affiliation country:
Complejo Hospitalario Universitario de Albacete/España
