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1.
Endocr Dev ; 22: 194-207, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-22846530

RESUMEN

Ovarian masses are the most frequent gynecological pathology seen in adolescent girls. Functional or organic tumors of the ovary are usually benign and the incidence rises with age. Most cysts are functional and adnexal torsion is the main complication, but a malignant etiology must nevertheless always be eliminated. The clinical presentation is quite variable. Ultrasonography is the investigation of choice: the sonogram will reveal a strictly fluid, benign functional cyst, suggest an adnexal torsion, and provide evidence of a heterogeneous mass. Emergency surgery is indicated only in the case of suspected ovarian torsion, in order to perform detorsion. In all other cases, serum tumor marker measurements will orient the diagnosis and MRI is an essential complement to imaging of tumors with heterogeneous solid components. Surgery and histopathological examination then determine the stage and the benign or malignant nature of the mass. Ovarian tumors are classified by the World Health Organization based on the cell of origin into epithelial tumors, germ cell tumors and sex cord-stromal tumors. Surgery should always follow oncological standards and be as conservative as possible to preserve future fertility.


Asunto(s)
Ovario/crecimiento & desarrollo , Adolescente , Factores de Edad , Femenino , Humanos , Modelos Biológicos , Tamaño de los Órganos/fisiología , Enfermedades del Ovario/diagnóstico , Enfermedades del Ovario/diagnóstico por imagen , Enfermedades del Ovario/patología , Enfermedades del Ovario/cirugía , Ovario/anatomía & histología , Ovario/embriología , Ovario/patología , Ultrasonografía
2.
Gynecol Obstet Fertil ; 39(9): 521-4, 2011 Sep.
Artículo en Francés | MEDLINE | ID: mdl-21840746

RESUMEN

Klinefelter's syndrome (KS) affects one in 600 men and Turner's syndrome (TS), one in 2500 women. These 2 diseases are the most sex chromosome disorders characterized by one extra X in the SK male (47XXY) and the loss of an X in the girls with ST (45 X). Their common characteristic is the gonadal dysgenesis, which is the main cause of male or female infertility. Called "the forgotten syndrome", KS is under-diagnosed because apart from the large size, there are no dysmorphic features, along with a great ignorance of cognitive and language disorders in children. There are often comorbidities that lead to diagnosis such as autoimmune diseases or metabolic syndrome. TS is often diagnosed by the short stature. Management of Turner's girls has profoundly changed with Growth hormone therapy. There is an international consensus for a better management of associated diseases such as ORL, cardiac, renal, hepatic, autoimmune and metabolic diseases. Prenatal diagnosis allows early detection and management of cognitive deficiencies and of associated diseases.


Asunto(s)
Síndrome de Klinefelter/diagnóstico , Síndrome de Klinefelter/terapia , Síndrome de Turner/diagnóstico , Síndrome de Turner/terapia , Trastornos del Conocimiento/etiología , Trastornos del Conocimiento/genética , Trastornos del Conocimiento/terapia , Femenino , Disgenesia Gonadal/etiología , Disgenesia Gonadal/genética , Humanos , Infertilidad/etiología , Infertilidad/genética , Síndrome de Klinefelter/complicaciones , Trastornos del Lenguaje/etiología , Trastornos del Lenguaje/genética , Trastornos del Lenguaje/terapia , Masculino , Embarazo , Diagnóstico Prenatal , Síndrome de Turner/complicaciones
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