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EVALUATION AND MANAGEMENT OF AMENORRHEA Mazen Freij , MBBS MRCOG Assistant Professor at JUH. Objectives. Know the definition of Amenorrhea and Oligomenorrhea Understand the endocrine, genetic and anatomical basis for these disorders. Definitions. Primary amenorrhea
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EVALUATION AND MANAGEMENT OF AMENORRHEA MazenFreij, MBBS MRCOG Assistant Professor at JUH
Objectives • Know the definition of Amenorrhea and Oligomenorrhea • Understand the endocrine, genetic and anatomical basis for these disorders
Definitions • Primary amenorrhea • No menses by age 14, absence of 2º sexual characteristics. • No menses by age 16 , presence of 2º sexual characteristics.
Secondary amenorrhea No menses for 3 months if previous menses were regular. No menses for 6 months if previous menses were irregular
Oligomenorrhea • Interval of more than 35 days between periods
Neural control Chemical control Dopamine (-) Norepiniphrine (+) Endorphines (-) Hypothalamus Gn-RH ? ± – Ant. pituitary FSH, LH Ovaries Estrogen Progesterone Uterus Menses
AMENORRHOEA AN APPROACH FOR DIAGNOSIS • HISTORY • PHYSICAL EXAMINATION • BLOOD TESTS • ULTRASOUND EXAMINATION Exclude Pregnancy Exclude Cryptomenorrhea
Cryptomenorrhea • Outflow obstruction to menstrual blood • -Imperforate hymen • - Transverse Vaginal septum with functioning uterus • - Isolated Vaginal agenesis with functioning uterus • - Isolated Cervical agenesiswith functioning uterus
Amenorrhea and no breast development. FSH Serum level Low / normal High Hypogonadotropic hypogonadim Gonadal dysgenesis
Amenorrhea and normal breast development. • - FSH, LH, Prolactin, TSH • Provera 10 mg PO daily • x 5 days + Bleeding No bleeing Prolactin TSH - Mild hypothalamic dysfunction - PCO (LH/FSH) Further Work-up (Endocrinologist) Review FSH result And history (next slide)
Amenorrhea Utero-vaginal absence Karyotype 46-XY 46-XX AndogenInsenitivity (TSF syndrome) Rokitanskysyndrome) Normal breasts & absent sexual hair Normal breasts & sexual hair
Amenorrhea • PRIMARY AMENORRHEA • . Ovarian failure • . Hypogonadotrophic • Hypogonadism. • . PCOS • . Congenital lesions • (other than dysgenesis) • . HypopituitarismHyperprolactinaemia • . Weight related • SECONDARY AMENORRHEA • . Polycystic ovary syndrome • . Premature ovarian failure • . Weight related amenorrhoea • . Hyperprolactinaemia • . Exercise related amenorrhoea • . Hypopituitarism
Gonadaldysgeneis • Classic turner’s syndrome (45XO) - Turner variants (45XO/46XX),(46X-abnormal X) - Mixed gonadaldygenesis (45XO/46XY)
Turner’s syndrome •Sexual infantilism and short stature. • Associated abnormalities, webbed neck,coarctation of the aorta,high-arched pallate, cubitus valgus, broad shield-like chest with wildely spaced nipples, low hairline on the neck, short metacarpal bones and renal anomalies. • High FSH and LH levels. • Bilateral streaked gonads. • Karyotype - 80 % 45, X0 - 20% mosaic forms (46XX/45X0) • Treatment: HRT
Turner’s syndrome (Classic 45-XO) Mosaic (46-XX / 45-XO)
Hypogonadotrophic Hypogonadism Normal hight Normal external and internal genital organs (infantile) Low FSH and LH 30-40% anosmia (kallmann’s syndrome) Treat with HRT
Constitutional pubertal delay • delayed bone age ( X-ray Wrist joint) • Positive family history • Diagnosis by exclusion and follow up
Weight-related amenorrhoeaAnorexia Nervosa • 1o or 2o Amenorrhea is often first sign • A body mass index (BMI) <17 kg/m² menstrual irregularity and amenorrhea • Hypothalamic suppression • Low estradiol risk of osteoporosis • Treatment : body wt. (Psychiatrist referral)
Utero-vaginal Agenisis Mayer-Rokitansky-Kuster-Hauser syndrome • Second most common cause of Primary amenorrhea. • Normal breasts and Sexual Hair Normal looking external female genitalia • Karyotype46-XX • 15-30% renal abnormalities. • Treatment : Vaginal creation (Dilatation VS Vaginoplasty)
Androgen insensitivityTesticular feminization syndrome • Normal breasts but no sexual hair • Normal looking female external genitalia • Absent uterus and upper vagina • Karyotype46, XY • Male range testosterone level • Treatment : gonadectomy after puberty + HRT
Amenorrhea • Endocrine causes. • Genetic causes. • Anatomic causes.
A 17-year-old girl presents to the clinic for the evaluation of primary amenorrhea.Which would be an important aspect of her clinical history? • A. History of leukemia during infancy • B. Short stature • C. History of delayed puberty in the family • D. All of the above • E. None of the above
After receiving Chemotherapy, which of the following labs results would make you consider the diagnosis of ovarian failure? • FSH of 60 IU/L (normal 0.33–10.54) • B. Estradiol of 100 pg/ml (normal 40–410) • C. LH of < 0.2 IU/L (normal 0.69–7.15) • D. All of the above • E. None of the above
The commonest cause for primary amenorrhea is • A. Turner Syndrome • B. CAH • C. Rokitansky Syndrome • D. Imperforsted Hymen • E. PCOS
One of the following can be the cause for primary amenorrhea with normal secondary sexualdevelopment. • A. Imperforated hymen. • B. Turner Syndrome • C. Androgen insensitivity. • D. Rokitansky syndrome • E. Hypogonadotropichypogonadism
19 year old presented with primary amenorrhea, normal breast development but no pubic hair, absent uterus. The most likely diagnosis is: • A. Rokitansky syndrome • B. Turner Syndrome • C. Androgen insensitivity • D.HypogonadotropicHupogonadism