Menstruation Flashcards
Average menarche age
12-13 YO
Average age of menopause
51
normal cycle
24-38 days
<8 dyas long
5-80 mL blood (30 mL = average)
Primary amenorrhea is considered
absence of menstruation by 15 YO w/ secondary characteristics
OR
absence by age 13 w/o secondary characteristics
secondary amenorrhea is considered
no period for 3 cycles
OR
6 consecutive months in women who were previously menstruating
Causes of primary amenorrhea
gonadal dysgenesis/ POI (most common)
Hypothalamic or pituitary
Outflow tract disorders
receptor abnormality or enzyme deficiency
Dysgensis results in
hypergonadotropic hypogonadism
Turner syndrome
45 XO
ovaries don’t respond to gonadtropins (one of most common causes of premature ovarian failure)
Results in premature depletion of oocytes and follicles
Presentation of turners
short, webbed neck, wide nippl
“streak ovaries” and sexual infantilism
Swyer syndrome
46, XY
Mutation in SRY gene - gonads fail to differentiate into testes; lack of AMH, T, and DHT = female external & internal genitalia
NO SECONDARY SEX CHARACTERISTICS (in contrast to AIS)
male appears like female
POI
46, XX w/ menopause before age 40
usually presents as secondary amenorrhea but can present as primary
Causes of POI
chemo
radiation
FX (FMR1 gene mutation)
autoimmune oophoritis
PCOS
rarely causes primary amenorrhea
ovulatory dysfunciton
hyperandrogenism w/ amenorrhea in absence of other causes
Hypogonadotropic hypogonadism
low FSH due to:
- abnormal hypothalamic GnRH secretion (leaing to decreased gonadotropin pulse d/c)
- congenital absence of GnRH
Hypothalamic amenorrhea
abnormal GnRH secretion in absence of patho process; decreased FSH/LH pulsations, low or normal FSH & LH, absent LH surge (absent follicular development & ovulation; low estradiol secretion)
Causes of hypothalamic amenorrhea
stressors (eating disorders, physical or psychological stress, weight loss, excessive exercise – female athletes triad)
Kallmann’s syndrome
idiopathic hypogonadotropic hypogonadism (congenital GnRH deficiency) + anosmia
Pituitary causes of primary amenorrhea
- micro/macroadenomas (cushings, prolactinomas, thyrotropinomas)
- Isolated hyperprolactinemia (mainly secondary amennorhea): causes galactorrhea, hypothyroidism & some meds increase prolactin levels
- infiltrative disease/cranial tumors that cause pituitary stalk compression (sarcoid, hemochromatosis)
Outflow tract disorders
Uterine- Mullerian Agenesis (vaginal agenesis)
Vagina- Imperforate hymen & transferse vaginal septum
Mullerian agenesis
46, XX w/ congenital absence of oviducts, uterus and upper vagina (normal gonad function: estrogen - breasts)
Imperforate hymen & transferse vaginal septum presentation
cyclic pelvic pain & perirectal mass from sequestration of blood in vagina
Androgen insensitivity syndrome (receptor/enzyme abnormality)
46, XY w/ female phenotype
Abnormality of androgen receptor (complete or partial)
- testes make T and AMH but body is not responsive
- high T concentrations!!!
Have breast development, absence of acne, & voice changes at puberty & absent axillary/pubic hair
Dx for AIS
Pelvic US- absent upper vagina, uterus & fallopian tube; tests remain in intra-abdominal or partially descended (mistaken for hernia)
Tx for AIS
remove testes (risk of testicular CA)
5-alpha reductase deficiency
46, XY
can’t convert T to DHT (no differentiation of male genitaliea)
AMBIGUOUS GENITALIA @ BIRTH
Undergo virilization @ puberty but no enlargement of external genitalia or prostate
Ambiguous genitalis
5-alpha reductase deficiency
17-alpha hydroxylase deficiency
46, XX or XY
lack enzyme to produe cortisol or sex steroids; overproduction of mineralcorticoids (high ACTH)
Presentation of 17-alpha deficiency
female w/ HTN and lack of pubertal development
OR
46, XY w/ incompletely developed external genitalia
HTN
17-alpha hydroxylase deficiency
When to initiate eval for amenorrhea
15 w/ no bleeding
13 w/ no menses or thelarche
No menarche w/i 3 years of thelarch
Order of sexual development
thelarche > pubarche > growth spurt > menarche
“boobs, pubes, grow, flow”
Anosmia
Kallman Syndrome
Virilization/hirsutism
PCOS
Labs for primary amenorrhea
Urine/serum HCG serum FSH prolactin TSH Pelvic u/s (uterus?)
no uterus: karyotype & total T (mullerian agenesis (XX) or AIS (XY))
elevated FSH: Karyoptype (XO = turner, XY = swyer)
FSH low/normal:
+ breast: outflow tract or endocrine (PCOS, hyperprolactinemia, thyroid disease)
- breast: recheck FSH, LH, consider pituitary MRI (congenital GnRH deficiency or constitutional delay of puberty)
Tx for primary amenorrhea
based on underlying etiology
Goals:
- treat cause
- restore ovulatory cycle/preserve fetility
- prevent complications (hypoestrognemia - osteoporosis)
Psych counseling
Refer to endocrinologist/gyne
Surgical referral for outlet obstruction or gonadectomy
Causes of secondary amenorrhea
PREGNANCY
Ovarian dysfunction
Hypothalamic dysfunction
Pituitary dysfunction
Uterine dysfunction
PCOS
2/3 to diagnose:
- androgen excess (acne, hirsutisim, elevated T)
- ovulatory dysfunction (amenorrhea or oligomenorrhea
- polycystic ovaries