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Amenorrhea

Amenorrhea is the absence of menstruation. It is classified as either primary amenorrhea or secondary amenorrhea depending on whether menarche has occurred. Causes include physiological factors (e.g., pregnancy, lactation, menopause), dysfunction of the hypothalamic-pituitary-gonadal axis, anatomical reproductive tract abnormalities, gonadal dysfunction, and systemic diseases. Clinical evaluation involves a focused history and physical examination, including a pelvic examination, Tanner staging, and evaluation for signs of common causes of amenorrhea. All individuals with amenorrhea should be evaluated for pregnancy and, based on clinical evaluation, receive targeted testing for suspected causes. Causes of primary amenorrhea are often identified with clinical evaluation and, if indicated, pelvic ultrasound and certain laboratory studies (e.g., FSH, karyotype). Causes of secondary amenorrhea are identified using hormone testing and often a pelvic ultrasound, followed by additional testing if indicated. Management focuses on the underlying cause and may include lifestyle changes, hormone replacement therapy (HRT), surgical correction for anatomical abnormalities, and infertility treatment.

Amenorrhea is the absence of menstruation; it is classified as either primary amenorrhea or secondary amenorrhea.

  • Primary amenorrhea: no menarche by 15 years of age or 5 years after thelarche, whichever comes first [1]
  • Secondary amenorrhea is the absence of menstruation for more than: [1]
    • 3 months in individuals with previously regular cycles
    • 6 months in individuals with previously irregular cycles

Delayed puberty in female individuals is defined as an absence of breast development by 13 years of age, and its workup includes an evaluation for causes of primary amenorrhea. [1][2]

Physiological causes [1][3][4]

  • Pregnancy
  • Lactation
  • Menopause
  • Constitutional delay of growth and puberty

Pregnancy, lactation, and menopause are the most common causes of amenorrhea. [1]

Reproductive tract abnormalities [1][3][4]

  • Transverse vaginal septum
  • Imperforate hymen
  • Agenesis of the lower vagina
  • Uterine adhesions (e.g., Asherman syndrome)
  • Cervical stenosis
  • Müllerian agenesis
  • Individuals with XY chromosomes and receptor or enzyme defects, e.g.:
    • 17α-hydroxylase deficiency
    • Androgen insensitivity syndrome
    • 5α-reductase deficiency

Ovulatory dysfunction [1][3][4]

Ovulatory dysfunction includes abnormalities ranging from occasional menstrual cycle irregularities to chronic anovulation. [5]

  • Primary ovarian insufficiency (hypergonadotropic hypogonadism)
  • Secondary ovarian insufficiency: hypothalamic or anterior pituitary dysfunction (hypogonadotropic hypogonadism) [6][7]
    • Functional hypothalamic amenorrhea
    • CNS:
      • Injury (e.g., TBI, radiation-induced brain injury)
      • Infiltration (e.g., in sarcoidosis, hemochromatosis)
      • Infection (e.g., meningitis)
      • Infarction (e.g., in Sheehan syndrome after severe postpartum hemorrhage)
    • Idiopathic hypogonadotropic hypogonadism (Kallmann syndrome in patients with anosmia)
    • GnRH suppression
      • Hyperprolactinemia; (e.g., due to pituitary adenoma; , medications, chronic kidney disease; , hypothyroidism)
      • Cushing syndrome
      • Chronic liver disease [8]
      • Medications (e.g., hormonal contraceptives)
  • Hyperandrogenic anovulation [9]
    • Polycystic ovary syndrome (PCOS)
    • Congenital adrenal hyperplasia
    • Androgen-producing tumors
    • Obesity [10]
Pathophysiology of primary amenorrhea
Mechanism and examples GnRH FSH and LH Estrogen and progesterone
Constitutional
growth delay
  • Normal pubertal development, but adrenarche and gonadarche occur at a later age
  • ↓ (at the prepubertal level)
Hypogonadotropic
hypogonadism
  • Caused by deficient release of GnRH
  • Examples
    • Kallmann syndrome
    • Competitive sports, stress, eating disorders
    • CNS tumors (e.g., craniopharyngioma)
  • Normal or ↓
Hypergonadotropic
hypogonadism
  • GnRH is released but the ovaries fail to produce estrogen and progesterone.
  • Examples: gonadal dysgenesis
    • 46, XY gonadal dysgenesis
    • Turner syndrome
Anatomic anomalies
  • Absent uterus and/or reproductive outflow tract obstruction with otherwise normal puberty
  • Examples
    • Müllerian agenesis
    • Imperforate hymen
    • Agenesis of the lower vagina
    • Transverse vaginal septum
  • Normal
  • Normal
  • Normal
Receptor and enzyme abnormalities
  • Examples
    • Complete androgen insensitivity syndrome
    • 5-alpha-reductase deficiency
  • Normal
  • Normal or ↑
  • Normal or ↓

Focused history [1][3]

  • Gynecologic and obstetric history
    • Age at thelarche and menarche
    • Menstrual history
    • Sexual history (e.g., sexual activity, history of STIs)
    • Recent pregnancy or breastfeeding
  • Past medical history
    • Medication use (e.g., antipsychotics, oral contraceptives)
    • Preexisting medical conditions
    • History of chemotherapy
  • Focused review of symptoms
    • Symptoms of estrogen deficiency
    • Symptoms of hypothyroidism or symptoms of hyperthyroidism
    • Symptoms of eating disorders, including excessive exercise
    • Symptoms of hyperandrogenism
    • Symptoms of hyperprolactinemia (e.g., galactorrhea)
  • Psychosocial stressors

Physical examination [1][3]

  • Blood pressure
  • BMI
  • Assessment for dysmorphic features (e.g., signs of Turner syndrome)
  • Examination of the thyroid gland
  • Evaluation for signs of hyperandrogenism (e.g., hirsutism, acne)
  • Tanner stage
  • Pelvic examination to assess for:
    • Structural abnormalities (e.g., imperforate hymen, transverse vaginal septum, blind or absent vagina)
    • Signs of low estrogen (e.g., prepubertal appearance, urogenital atrophy) [11][12]

Hypertension may be present in patients with congenital adrenal hyperplasia due to 17α-hydroxylase deficiency or in patients with Cushing syndrome. [1][13]

Approach [1][3]

Obtain a pregnancy test in all patients before initiating a diagnostic workup for amenorrhea.

Primary amenorrhea

  • Cervix visualized on pelvic examination (i.e., a uterus is present): Obtain FSH; consider also obtaining other initial laboratory studies for amenorrhea.
    • FSH or normal
      • Breasts absent: Evaluate for constitutional delay of growth and puberty and isolated GnRH deficiency (e.g., Kallmann syndrome).
      • Breasts present: Perform workup for secondary amenorrhea.
    • FSH: Perform karyotyping to evaluate for genetic causes of primary ovarian insufficiency (gonadal dysgenesis).
  • Blind or absent vagina on pelvic examination: Perform pelvic ultrasound to assess internal reproductive organs.
    • Uterus absent: Perform karyotyping and measure testosterone level.
    • Uterus present: Consider ; congenital reproductive outflow tract obstruction (e.g., imperforate hymen, vaginal agenesis, and transverse vaginal septum).
  • See “Common causes of primary amenorrhea” for further details on interpretation of findings.

Secondary amenorrhea

  • Obtain:
    • Initial laboratory studies for amenorrhea
    • Targeted testing for amenorrhea as clinically indicated
    • Pelvic ultrasound, if readily available
  • See “Common causes of secondary amenorrhea” for further details on interpretation of findings.
  • If no cause is identified, consider hormone withdrawal testing for amenorrhea.

Initial laboratory studies for amenorrhea [1][3]

Tests commonly obtained include the following:

  • FSH with or without LH
  • Estradiol with or without anti-Müllerian hormone (AMH)
  • TSH
  • Prolactin

Targeted testing for amenorrhea [1][3]

Obtain targeted testing as indicated by clinical presentation, if not already obtained as part of initial testing.

  • Laboratory studies
    • Signs of estrogen deficiency: FSH, LH, estradiol, AMH
    • Signs of hyperandrogenism: free and total testosterone, DHEA-S, 17-hydroxyprogesterone
    • Signs of hyperprolactinemia (e.g., galactorrhea): prolactin
    • Signs of hypothyroidism or signs of hyperthyroidism: TSH
    • Signs of adrenal insufficiency or hypercortisolism: cortisol
    • Signs of chronic systemic illness: CBC, BMP, ESR, CRP, urinalysis
    • Weight loss and/or gastrointestinal symptoms: diagnostics for celiac disease
  • Imaging
    • Suspected PCOS and/or structural reproductive tract abnormalities: pelvic ultrasound or MRI
    • Suspected androgen-secreting tumor: adrenal imaging
    • Symptoms suggestive of CNS pathology (e.g., visual field defects) and/or persistent hyperprolactinemia: MRI brain

TSH suggests hypothyroidism as a cause of amenorrhea.

Elevated levels of androgens (testosterone, DHEA-S) can be seen with PCOS, congenital adrenal hyperplasia, Cushing syndrome, or an androgen-secreting tumor. [3]

Hormone withdrawal testing in amenorrhea [14]

The following studies can be used to evaluate patients with secondary amenorrhea if there is no identified cause after the initial workup. [1]

  • Progestin challenge test: typically the initial test
    • Method: Administer a progestin for 5–10 days. [15]
    • Interpretation: Assess for withdrawal bleeding within 14 days of progestin cessation.
      • Withdrawal bleeding: indicates anovulation (e.g., PCOS, idiopathic anovulation)
      • No withdrawal bleeding: indicates hypoestrogenism (i.e., hypogonadism) or reproductive outflow tract obstruction
  • Estrogen-progesterone challenge test: performed in patients with no withdrawal bleeding on initial testing
    • Method
      • Administer estrogen for 21–25 days.
      • Add progesterone during the last 5–10 days of estrogen administration.
    • Interpretation: Assess for withdrawal bleeding within 2–7 days of progesterone cessation.
      • Withdrawal bleeding: indicates hypoestrogenism (i.e., hypogonadism)
      • No withdrawal bleeding: indicates reproductive outflow tract obstruction or endometrial dysfunction (e.g., Asherman syndrome; , endometritis)

Primary amenorrhea [1][3]

Most causes of secondary amenorrhea can also cause primary amenorrhea.

Common causes of primary amenorrhea [1][3]
Characteristic clinical features Diagnostic findings Management
Constitutional delay of growth and puberty [2][16]
  • No thelarche by 13 years of age
  • Short stature with normal prepubertal growth velocity
  • Family history of constitutional delay of growth and puberty
  • Prepubertal levels of FSH and LH
  • Delayed bone age
  • Diagnosis of exclusion
  • Observation and reassurance
  • Consider HRT with low-dose estrogen.
  • Refer to endocrinology if delay persists for > 6 months. [16]
Gonadal dysgenesis
  • Absent or incomplete breast development
  • Decreased androgenic signs (e.g., scant pubic hair)
  • Dysmorphic features in individuals with Turner syndrome
  • FSH and LH
  • Streak gonads on pelvic ultrasound
  • Karyotype is often abnormal.
    • Turner syndrome (most common): 45,XO
    • Others: 46,XX or 46,XY
  • HRT
  • Refer to endocrinology and genetics.
Isolated GnRH deficiency [17][18]
  • Absent or incomplete breast development
  • Kallmann syndrome: self-reported anosmia or hyposmia
  • FSH and LH
  • Kallmann syndrome
    • Olfactory function test: anosmia or hyposmia
    • MRI brain: olfactory bulb hypoplasia or aplasia
  • HRT
  • Infertility treatment
  • Refer to endocrinology.
Androgen insensitivity syndrome [19]
  • Breasts present
  • Absent or scant pubic and axillary hair
  • Pelvic examination: blind vaginal pouch
  • Pelvic ultrasound or MRI
    • Absent Müllerian duct stuctures
    • Intra-abdominal or inguinal testes
  • Testosterone (male range)
  • Karyotype: 46,XY
  • Specialist referral for management depending on patient presentation and preference
Imperforate hymen or transverse vaginal septum [20]
  • Normal secondary sex characteristics
  • Cyclic or continuous pelvic pain
  • Palpable lower abdominal mass
  • Pelvic examination: hematocolpos and non-visualized cervix
  • Clinical diagnosis
  • Pelvic imaging can be used to visualize anatomy before surgery if indicated.
  • Hymenectomy
  • Vaginal septum resection
Agenesis of the lower vagina [20][21]
  • Normal secondary sex characteristics
  • Cyclic or continuous pelvic pain
  • Palpable lower abdominal mass
  • Pelvic examination: absent (dimple) or shortened, nonpatent vagina
  • Absent lower vagina
  • Ovaries and Müllerian duct stuctures present on pelvic imaging
  • Vaginal dilation
  • Vaginoplasty
Müllerian agenesis [19]
  • Normal secondary sex characteristics
  • Possible cyclic or continuous pelvic pain
  • Pelvic examination: absent (dimple) or shortened vagina
  • Rudimentary or absent Müllerian duct structures on pelvic imaging
  • Congenital urological and skeletal abnormalities on imaging
  • Vaginal elongation
  • Vaginoplasty

Secondary amenorrhea [1][3]

Pregnancy, breastfeeding (lactation amenorrhea), and menopause are the most common causes of secondary amenorrhea.

Common causes of secondary amenorrhea [1][3]
Characteristic clinical features Diagnostic findings Management
Menopause
  • Age ≥ 40 years
  • Vasomotor symptoms
  • Genitourinary syndrome of menopause
  • FSH, estradiol [22]
  • AMH
  • Symptom-specific nonpharmacological interventions for menopause
  • HRT for moderate to severe symptoms
  • See “Treatment of menopause.”
Polycystic ovary syndrome
  • Clinical features of PCOS (e.g., signs of hyperandrogenism, acanthosis nigricans)
  • LH:FSH ratio, AMH, and androgens
  • Enlarged or polycystic ovaries on pelvic ultrasound
  • Lifestyle changes
  • Pharmacological treatment (e.g., COCs, metformin)
  • See “Treatment of PCOS.”
Thyroid disorders
  • Symptoms of hypothyroidism
  • Symptoms of hyperthyroidism
  • Abnormal thyroid examination (e.g., thyromegaly)
  • Hypothyroidism: TSH
  • Hyperthyroidism: TSH
  • See “Treatment of hypothyroidism” and “Treatment of hyperthyroidism.”
Hyperprolactinemia
  • Galactorrhea
  • If CNS involvement: headaches, visual changes
  • Prolactin
  • MRI pituitary may show a pituitary adenoma.
  • Prolactinoma: dopamine agonists (bromocriptine, cabergoline)
  • Refer to endocrinology.
  • See “Treatment of hyperprolactinemia.”
Nonclassic CAH due to 21β-hydroxylase deficiency [23][24]
  • Signs of hyperandrogenism
  • Precocious puberty
  • 17-hydroxyprogesterone
  • Positive ACTH stimulation test
  • Combined oral contraceptives
  • Glucocorticoid therapy
  • Antiandrogen therapy
Primary ovarian insufficiency
  • Age < 40 years
  • Vasomotor symptoms
  • Vaginal dryness
  • FSH, estradiol
  • AMH
  • Management of the underlying cause
  • HRT
Functional hypothalamic amenorrhea [15]
  • Signs of estrogen deficiency
  • Excessive exercise, calorie deficit, low BMI
  • Stress
  • Diagnosis of exclusion
  • ↓ or normal LH, normal FSH, estradiol
  • Management of the underlying cause
  • See “Functional hypothalamic amenorrhea.”
Acquired reproductive outflow tract obstruction
  • Prior cervical or uterine instrumentation or trauma
  • Cyclical or continuous pelvic pain in individuals with cervical stenosis
  • Normal hormone levels
  • Negative hormone withdrawal testing in amenorrhea
  • Abnormal findings on hysteroscopy (e.g., cervical stenosis, intrauterine adhesions)
  • Procedural interventions (e.g., cervical dilation, lysis of uterine adhesions)

Management is based on the underlying cause. [1][3]

  • Goals
    • Progression of puberty in patients with primary amenorrhea
    • Prevention of complications (e.g., osteoporosis, symptoms of estrogen deficiency)
    • Optimization of reproductive health (e.g., functional anatomy, fertility)
  • Options
    • Lifestyle changes (e.g., in PCOS, functional hypothalamic amenorrhea)
    • Pharmacological treatment, e.g.:
      • HRT and COCs for hypogonadism
      • Dopamine agonists (bromocriptine, cabergoline) for prolactinoma
    • Surgery for tumors or anatomical abnormalities
  • Indications for specialist referral
    • Procedural interventions: gynecology or surgery
    • Hormonal abnormalities: endocrinology
    • Infertility treatment: reproductive endocrinology