Endocrinology Flashcards

1
Q

What regulates prolactin release?

A

Under inhibition from dopamine

More dopamine = less prolactin

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2
Q

What is the strongest osmolar stimulant of ADH osmoreceptors?

A

Sodium

Next is mannitol

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3
Q

What is the most potent known stimulus to ADH?

A

Nausea

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4
Q

What osmolality does thirst begin?

A

295 mOsm/kg

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5
Q

True or false. Prolactin levels are high in hypothyroidism.

A

True

Prolactin elevates with primary hypothyroidism, and with any inhibition of dopamine from hypothalamus

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6
Q

What is septooptic dysplasia?

A

Abnormality of the optic nerve, agenesis or hypoplasia of . the septum pellucidum or corpus callosum, and various degrees of hypothalamic insufficiency

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7
Q

Which endocrine abnormality do you look for if a patient has a solitary maxillary incisor

A

High likelihood of GH deficiency

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8
Q

Which structure is key in determining the level of pituitary involvement in a patient with an ectopic posterior pituitary?

A

Anterior pituitary problems

Stalk:
Normal stalk - isolated GH def
Abnormal stalk - multiple pit hormone def

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9
Q

What is the most common tumour to cause pituitary hormone deficiency

A

Craniopharyngioma

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10
Q

What are the clinical clues that make you suspect congenital GH deficiency?

A

Normal length and weight at birth
Micropenis
Hypoglycaemia
Prolonged direct hyperbilirubinaemia

Falling off growth curve after 3 years

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11
Q

What is idiopathic short stature?

A

Normal children who are short >2.25SD below mean but have normal GH secretion

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12
Q

True or false. Children with constitutional growth delay typically require GH to reach normal adult height

A

False

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13
Q

What is Russel Silver syndrome

A

Short stature, frontal bossing, triangular facies, shortened and incurved 5th fingers, asymmetry
SGA and FTT

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14
Q

Which children with short stature are FDA approved to receive GH to reach a more normal height

A
ISS who are unlikely to reach normal adult height 
Chronic renal insufficiency 
Turner syndrome
Prader Willi syndrome 
Noonan
SGA (if not caught up by 2yo)
SHOX
AIDs wasting syndrome
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15
Q

Child with severe head injury 3/7 ago, now severe hyponatremia, what aetiology should you consider

A

Central diabetes insipidus

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16
Q

What is the most common medication to cause nephrogenic DI

17
Q

how is SIADH best managed

A

Fluid restriction

18
Q

Name 3 abnormal causes of tall stature

A

Klienfelter
Marfan
Homocystinuria

19
Q

What is Beckwith Wiedemann syndrome

A

Overgrowth syndrome
Macroglossia, hepatosplenomegaly, nephromegaly, pancreatic B cell hyperplasia

Predisposed to Wilms tumor, adrenocortical carcinoma and hepatoblastoma

20
Q

What is Sotos syndrome

A

Syndrome - rapid growth in childhood with no evidence of endocrine disorder
Born above 90th and grow rapidly in 1st year to >97th

21
Q

How might an adolescent female present with prolactinoma

A

Headache, amenorrhoea, galactorrhoea

22
Q

What is the best way to diagnose prolactinoma

A

MRI of sella

23
Q

Risk with GH treatment

A

No inc risk of leukaemia

SCFE, pseudotumor cerebri, transient carb intolerance, transient hypothyroidism and scoliosis

24
Q

Hormone for initiation of puberty?

25
How long for menarche after initial signs of puberty (girls)
2-2.5yrs
26
When does peak height velocity occur in girls
11-12 years
27
mean menarche age
12.5 years
28
First signs puberty in boys
Testes enlargement
29
Which occurs first, penis enlargement or pubic hair
Testes -> penis lengthening -> pubic hair
30
When does growth spurt occur in boys
2 years later than girls
31
Lab results for central precocious puberty
Girls: adrenal and gonadal involvement Boys - gonadal involvement LH spikes
32
Most common brain lesion - CPP
Hypothalamic hamartoma
33
What causes peripheral precocious puberty?
Excess secretion of sex hormones from gonads, adrenal glands or germ cell tumours Exogenous exposure to sex steroids
34
What causes testes to grow
FSH