Male Hypogonadism Flashcards

1
Q

How is testosterone made?

A

Leydig cells

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2
Q

What kind of hormone is testosterone?

A

Sterois

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3
Q

How does Testosterone circulate in the blood?

A

Bound to SHBG or albumin

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4
Q

What enzyme reaction activates testesterone?

A

Testosterone -> dihydrotestosterone by 5-alpha reductase.

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5
Q

Where is testosterone activated?

A

In target tissues once it is free.

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6
Q

What is the role of testosterone?

A
  • Growth: sex organs, muscle, epiphyseal plates, larynx, secondary sex characteristics.
  • Other: Erythropoiesis, behaviour
  • Adults: Muscle mass, mood, bone mass, libido, body shape.
  • Fertility: Libido, erection and spermatogenesis.
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7
Q

What is the role of sertoli cells?

A

Maintain blood-testes barrier.
Remove damaged spermatocytes
Secrete androgen binding protein which locks testosterone in the tested.

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8
Q

What are the child symptoms of hypogonadism?

A
  • Slow growth in teens
  • No pubertal growth spurt
  • Lack of secondary sexual development
  • Small testes and phallus
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9
Q

What are the adult symptoms of hypogondadism?

A
- Small testes and short phallus
 low mood 
- poor libido
- erectile dysfunction 
- low muscle bulk/power 
- poor energy 
- sparse body/facial hair 
- gynacomastia 
- lots of hair on head.
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10
Q

What size of testes would be seen on an orchidometer in early puberty?
Mid puberty?
Late puberty?
Adult?

A

Early: 4-6
Mid: 8-10
Late: 12-15
Adult: 20-25

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11
Q

How do you test for hypogonadism?

A
  • Early morning testosterone (should be surge in the morning)
  • Free testosterone (normally >200)
  • Total testosterone (normally >16)
  • SHBG
  • LH/FSH (is it pituitary cause?
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12
Q

How would you test fertility in males?

A
  • Semen analysis: 1-3 days after last ejaculation, should be 2-5ml volume.
  • Check count, motility and morphology.
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13
Q

In hypogonadotrophic hypogonadism where is the problem?

A

Hypothalamus or pituitary.

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14
Q

In primary gonadal failure, where is the problem?

A

Testicles.

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15
Q

Give examples of causes of hypogonadotrophic hypogonadism?

A
  • pituitary surgery
  • radiotherapy
  • pituitary tumour
  • prolactinoma (high prolactin supresses LH and FSH)
  • ead injury
  • Kallmans syndrome,
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16
Q

What causes Kallmans syndrome?

A

Failure of cell migration of GnRH cells to the hypohlamus from the olfactory placode.

17
Q

How is Kallmans syndrome inerited?

A
Most commonly X-linked. Absence of KAL1 gene. 
Autosomal dominant (KAL2)
Autosomal recessive (KAL3)
18
Q

What are the symptoms of kallmans syndrome?

A

Same as hypogonadotropic hypogonadism with added symptom of anosmia or hyponosmia.

  • small penis and testes, lack of 2ndry sex characteristics, poor libido, erectile dysfunction, low muscle bulk, gynacomastia etc.
  • may have cryptorchidism, deafness, renal agenesis and cleft lip/palate.
19
Q

Describe testosterone, FSH, LH and prolactin in primary gonadal failure?

A

low testosterone

normal FSH, LH and prolactin.

20
Q

List causes of primary gonadal failure?

A
  • Trauma
  • Chemotherapy
  • Radiotherapy
  • Multisystem disorders
  • Kleinfelters
  • Myotonic dystrophy
21
Q

What is the gnetic abnormality in Kleinfelters?

A

XXY

22
Q

When does gonadal failure manifest in Kleinfelters?

A

At puberty

23
Q

How is primary gondalal failure managed?

A
  • Androgen replacement: HypoG treatment: oral, IM or topical. BUT this wont concentrate enough in the testes to regain fertility.
  • Physcological support and fertility councilling.
24
Q

List problems with androgen replacement therapy?

A
  • Mood issues (aggression or behaviour change)
  • Libido increased
  • Increased haematocrit (increased risk of stroke and heart disease)
  • Prostate enlargement (increased chance of BPH or cancer)
  • Gynacomastia due to increased aromatase increasing oestrogen.