GYNE Benign Disorders of the Upper and Lower Genital Tract, Blueprints Flashcards
Most common cause of labial fusion
Exogenous androgen
Most common form of enzymatic deficiency
21-hydroxylase deficiency
21-hydroxylase deficiency: Associated condition
Congenital adrenal hyperplasia (CAH)
Congenital adrenal hyperplasia (CAH): Hormone elevated
17α-hydroxyprogesterone
Congenital adrenal hyperplasia (CAH): Serum cortisol, increased vs decreased
Decreased
Congenital adrenal hyperplasia (CAH): Treatment
Exogenous cortisol
Congenital adrenal hyperplasia (CAH): Mechanism of exogenous cortisol
Negative feedback on pituitary > decrease ACTH > inhibition of adrenal gland stimulation > decrease in androgens
Primary amenorrhea + cyclic pelvic pain: Condition
1) Imperforate hymen
2) Transverse vaginal septum
3) Vaginal atresia
Accumulation of menstrual flow behind the hymen in the vagina
Hematocolpos
The caudal portion of the Müllerian ducts develops into
Uterus and upper vagina
Structure that must be canalised for normal vagina to form
Mullerian tubercle
Failure of mullein tubercle to canalise results in
Transverse vaginal septum
Most common site of transverse vaginal septum
Between upper 1/3 and lower 2/3
Occurs when the lower vagina is replaced by fibrous tissue and on PE reveals a vaginal dimple
Vaginal atresia
Vaginal atresia, management
Vaginal pull-through
Congenital absence of vagina and absence or hypoplasia of all or part of the cervix, uterus, and fallopian tubes
Vaginal agenesis
Vaginal agenesis is aka
Meyer-Rokitansky-Kuster-Hauser syndrome
T/F Ovary is hypoplastic in vaginal agenesis
F, normal
Vaginal agenesis: T/F Normal external genitalia
T
Vaginal agenesis: T/F Normal secondary sexual characteristics (breast development, axillary, and pubic hair)
T
Vaginal agenesis: T/F Normal ovarian function
T
Vaginal agenesis: T/F Phenotypically female
T
Vaginal agenesis: T/F Genotypically female
T
Vaginal agenesis: Management
1) Non-surgical with the use of dilators
2) Surgical