Male Hypogonadism Flashcards

1
Q

how is the majority of testosterone transported and how much is ‘free’

A

majority is bound to SHBG and albumin, only 0.5-2% is free

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2
Q

what is testosterone converted to

A

dihydrotestosterone and oestradiol

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3
Q

what is testosterone converted to dihydrotestosterone and oestradiol by

A

dihydrotestosterone by 5alpha reductase

oestradiol by aromatase

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4
Q

what is the definition of hypogonaadism

A

clinical syndrome comprising of signs, symptoms and biochemical evidence of testosterone deficiency

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5
Q

how does hypogonadism relate to age

A

incidence increases with age

2-5% in men 40-79y/o

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6
Q

what is the difference between primary and secondary hypogonadism

A
primary = caused by testes pathology
secondary = caused by something external to testes(eg hypothalamus or pituitary
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7
Q

what affect does decreased testosterone in primary hypogonadism have on the anterior pituitary and what does this lead to

A

decreases -ve feedback, so increases LH and FSH release, resulting in hypergonadotrophic hypogonadism

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8
Q

how are spermatogenesis and testosterone production affected in primary hypogonadism

A

both decreased, but spermatogenesis affected more

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9
Q

how are FSH, LH and testosterone affected in secondary hypogonadism and what does this lead to

A

FSH and LH low due to hypothalamic/pituitary dysfunction, testosterone low as result, leads to hypogonadotrophic hypogonadism

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10
Q

how are spermatogenesis and testosterone affected in secondary hypogonadism

A

both decreased and affected equally

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11
Q

what are some congenital causes of primary hypogonadism

A

Klinefelter’s syndrome, cryptorchidism, Y-chromosome microdeletion

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12
Q

what are some acquired causes of primary hypogonadism

A

testicular trauma/torsion, chemo/radiation, varicocele, orchitis, infiltrative disease, medications

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13
Q

what is the most common congenital/genetic cause of hypogonadism and how is it diagnosed

A

Klinefelter’s syndrome, diagnosed by karyotyping

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14
Q

what is the inheritance pattern seen in Klinefelter’s syndrome

A

not inherited, caused by nondisjunction

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15
Q

how is fertility and the testes affected in men with Klinefelter’s syndrome

A

typically infertile and testes are small and firm

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16
Q

what is there increased risk of in Klinefelter’s syndrome

A

increased incidence learning disability, crytporchidism, psychosocial issues
increased risk breast cancer and non-Hodgkin lymphoma

17
Q

what are some of the congenital causes of secondary hypogonadism

A

Kallmann’s syndrome Prader-Willi syndrome

18
Q

what are some of the acquired causes of secondary hypogonadism

A

pituitary damage, hyperprolactinaemia, obesity, DM, medications, acute systemic illness, eating disorders

19
Q

describe what Kallmann’s syndrome is

A

genetic syndrome characterised by isolated GnRH deficiency and hyposmia or anosmia

20
Q

what are the symptoms and signs associated with pre-pubertal onset of hypogonadism

A

small sexual organs, decreased body hair, high-pitched voice, low libido, gynaecomastia, ‘eunochoidal’ habitus, decreased bone/muscle mass

21
Q

what are the symptoms and signs associated with post-pubertal onset of hypogonadism

A

normal skeletal and sexual organ size, decreased libido and erections, decreased hair growth, decreased testicular volume, gynaecomastia, decreased muscle/bone mass, decreased energy/motivation