Oligo/Amenorrhoea Flashcards

1
Q

Define

  • primary amenorrhoea
  • secondary amenorrhoea
  • oligoamenorrhoea
A

Primary amenorrhoea- failure of menstruation by age 16
Secondary amenorrhoea- cessation of menstruation for over 6 months
Oligoamenorrhoea- menstruation occurring every 35 days to 6 months

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2
Q

How do you investigate amenorrhoea?

A
  1. Serum urine hCG
  2. LH and FSH
  3. Serum basal prolactin
  4. Testosterone- total testosterone, sex binding globulin, free testosterone
  5. TFT’s (TSH, T3 and T4)
  6. Transvaginal ultrasound
  7. Karyotyping
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3
Q
What would you see with the FSH and LH levels: 
ovarian failure 
Tuner's syndrome 
Testicular feminisation
Hypothalamic hypogonaidism 
Constitutional delay
A
  • raised in ovarian failure
  • raised in Turner’s: will also be shorter
  • raised in TF (receptors not responding)
  • decreased in Hypothalamic hypogonaidism
  • normal in constitutional delay
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4
Q

What causes hyperprolactinaemia?

A

Prolactinoma
Prolactin secreting tumour
Hypothyrodism
Head injury, brain surgery, irradiation
TB, Sarcoidosis, Sheehan’s syndrome (Secondary amenorrhoea)
Drugs- dopamine agonists, antidepressants, metacloparamide, opiates, cocaine, heroin

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5
Q

What is a raised prolactin levels, and how many times do you do the investigation?

What is the management of hyperprolactinaemia

A

> 1000, and do the test twice

  • Dopamine agonists: Bromocriptine
    Surgical removal if tumour
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6
Q

What are the adrenal causes of primary and secondary amenorrhoea?

A

Primary: Congenital adrenal hyperplasia, Testicular feminsisation, adrenal tumours
Secondary: Adrenal tumours

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7
Q

What is congenital adrenal hyperplasia and what are it’s features during infancy?

A
  • Due to 21- hydroxylase deficiency which results in cortisol (and or aldosterone) deficiency and androgen excess

Features
- ambigious genitalia
- Enlarged clitoris
- Urogenital sinus (instead of separate vagina and uterus)
If aldosterone deficiency- then nausea, vomiting, diarrhoea, weight loss, lethargy, dehydration, hypnoatraemia, hyperkalaemia, and shock

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8
Q

What is testicular feminisation and what are its clinical features?

A

X-linked disorder, genotype is male
Testosterone receptors are not sensitive to testosterone, so have peripheral conversion of testosterone to oestrogeon

  • External genitalia are feminine (vagina is blind ending) but have absence of uterus or ovaries
  • testes fail to descend normally in the groin
  • will have breast development and female contours
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9
Q

What are the ovarian causes of primary and secondary amenorrhoea?

A

Primary-Tuner’s syndrome, PCOS

Secondary- Premature ovarian failure, PCOS, virilizing ovarian tumours

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10
Q

What is a polycystic ovary

What is epidemiology of PCOS?

A

Polycyctsic ovary, when >12 follicles, small 2-8 cm follicles in enlarged ovary >10cm

Epidemiology: Obese women, causes 80% of infertility, patients present in prepubertal period to mid 20’s

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11
Q

What is pathophysiology of PCOS?

A
  • Have disordered LH production with high LH levels, and insulin resistance so high insulin levels
  • LH and insulin act on polycystic ovary which produced testosterone
  • Insulin also act on adrenal gland to produce testosterone
  • Insulin works on liver produces less steroid binding globulin
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12
Q

How do you diagnose PCOS

What are clin features of PCOS?

A

Rotterdam criteria (2 out 3): PCO ovary on transvaginal ultrasound, oligo-ovulation or amennorrhoea (periods >35 days apart) and clinical or biochemical signs of raised testosterone

Features

  • Oligoamenorrhoea (<9 periods a year), amenorrhoea
  • Subfertility
  • Miscarriage
  • Virilization: acne, hirsutism (upper lip, chin, nipple, umbilicus), clitomegaly, deep voice, increased muscle mass
  • Obesity, acanthosis nigricans
  • Alopecia
  • Psychological symptoms: low self esteem, mood swings, depression, anxiety, sleep aponea
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13
Q

What are investigations for PCOS?

A
  1. Serum bHCG
  2. FSH- normal
  3. Prolactin- exclude prolactinoma
  4. Testosterone- total testosterone (normal), free testosterone(raised) , steroid binding globulin (normal/reduced)
  5. HB1ac, lipids (increased cardiovascular risk)
  6. Transvaginal ultrasound- visualize polycystic ovary
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14
Q

What are complications of PCOS?

A
  • Dyslipidaemia and cardiovascular risk and type 2 diabetes

- Endometrial cancer (amenorrhoea means unopposed oestrogeon causes endometrial hyperplasia- cancer)

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15
Q

What is management of PCOS? (general and pharmacological)

A
  • Weight loss
    Not getting pregnant:
    -Cycle control: COCP (want 3-4 bleeds a year to protect endometrium) progesterone or Mirena IUS
  • Hirsutism: Topical Elfornithine, or spironolactone/cryptocerone acetate (all anti-androgens)
  • Metformin

Getting pregnant:

  • Clomifene (antioestrogeon)- max 6 months with TVS monitoring
  • Metformin used instead of clomifene to increase fertility
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16
Q

Which outflow tract problems may cause primary and secondary amenorrhoea?

A

Primary- Imperforate hymen, transverse vaginal septum

Secondary- Asherman’s syndrome and cervical stenosis

17
Q

What would be the features of an imperforate hymen and transverge vaginal septum?

A

Cyclical pain near menstrual cycle

O/E palpable haematocolpus (blood in vagina) and haematometra (blood in uterus)

18
Q

What causes cervical stenosis and Asherman’s syndrome?

A

Cervical stenosis- narrowing of cervix due to coloposcopy, trauma, repeated vaginal infections, atrophy, cervical cancer
Ashermnan’s syndrome- adhesions and fibrosis of endometrium secondary to excessive curettage at RPOC

19
Q

Which contraceptives cause amenorrhoea?

A
  • Mirena IUS

- Depot

20
Q

In how many months should post-pill amenorrhoea settle by?

A

-3 months