ABSTRACT
The Complete testicular feminization syndrome is a hereditary syndrome characterized clinically by female phenotype with 46, XY karyotype and bilateral testes. There is a congenital insensitivity to androgens, transmitted by means of a maternal X-linked recessive gene responsible for the androgen intracellular receptor. Therefore, androgen induction of Wolffian duct development does not occur. However, anti-mullerian hormone activity is present and the individual does not have mullerian development. Principle of treatment is reinforced to live normal female life. This is a case report of testicular feminization syndrome with rudimentary salpinx with the brief review of literatures.
Subject(s)
Female , Humans , Male , Androgen-Insensitivity Syndrome , Androgens , Anti-Mullerian Hormone , Fallopian Tubes , Genes, Recessive , Karyotype , Phenotype , Testis , Wolffian DuctsABSTRACT
No abstract available.
Subject(s)
Female , Pregnancy , Pregnancy , Cervical Ripening , Cervix Uteri , Dinoprostone , MisoprostolABSTRACT
Endometriosis is defined as the presence of endometrial tissue(gland and stroma) outside the uterus. The incidence of scar endometriosis is quite rare, and must differentiate with cellulitis and abscess. We have experienced one case of perineal endometriosis and one case of abdominal wall endometriosis at the site of postoperative wound scar. The possible pathogenesis of endometriosis and treatment were discussed.