Hypo secretion of Anterior Pituitary Hormones Flashcards

1
Q

Primary, secondary and tertiary endocrine gland diseases

A

Primary - Disorder at the endocrine gland
Secondary -disorder at the pituitary gland
Tertiary - disorder at the hypothalamus

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2
Q

Panhypopituitarism

A

Decreased production of all anterior pituitary hormones

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3
Q

Panhypopituitarism is caused by

A

Congenital –> rare defects or gene mutations in the genes involved in the development of the gland (e.g. PROP1). Hypo plastic pituitary gland

Acquired --> radiotherapy
tumours
infection
trauma
infiltrative disease
inflammatory
pituitary apoplexy
post partum infarction
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4
Q

Panhypopituitarism causes progressive loss of the hormones in this order:

A

Gonadotrophin’s (LH and FSH)
GH
Thyrotrophin
Corticotrophin (ACTH)

Prolactin deficiency is uncommon

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5
Q

Simmon’s disease is

Caused by…

A

Slow and insidious in onset. Panhypopituitarism

Various: infiltrative processes e.g. lymphocytic
Pituitary adenomas
Craniopharyngiomas
Cranial injury
Following surgery
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6
Q

Simmond’s disease symptoms due to….. and include results in/symptoms:

A

decreased function of the thyroid, adrenals, and gonads

Result: Oligomenorrhoea/ secondary amenorrhoea in women
Impotence in men
Decreased libido
Tiredness
Waxy skin
Loss of body hair 
Hypotension
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7
Q

Diagnosis of hypopituitarism can be made by

A

Biochemical diagnosis - using basal plasma levels of pituitary or target endocrine hormones. (hypothalamus pulsatile so one measurement shows nothing)

Provocation/stimulation test.
For ACTH and GH - induce stress, inject insulin to induce hypoglycaemia
For TSH - give TRH
For FSH/LH - give GnRH

Radiological analysis - can spot apoplexy (haemorrhage/infarction); adenoma; empty sella turcica

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8
Q

Sheehan’s syndrome is

A

Postpartum ypopituitarism specific in women

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9
Q

Sheehan’s syndrome is caused by

A

Post-partum haemorrhage –> hypovolaemic shock and blood loss.

Leads to pituitary infarction
Blood loss in the vasoconstrictor spasm of hypophyseal arteries and this leads to:
- Ischaemia of the pituitary (which is enlarged during pregnancy due to lactotroph hyperplasia).
- Necrosis of the pituitary

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10
Q

Panhypopituitarism will occur in adults with …

A

progressive loss of pituitary secretion

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11
Q

3 main types of Panhypopituitarism

A
  • Simmond’s Disease
  • Sheehan’s Syndrome
  • Pituitary Apoplexy
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12
Q

Presentation of Sheehan’s is

A

fast

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13
Q

Presentation of Pituitary apoplexy is

A

fast

in pituitary adenoma

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14
Q

Pituitary apoplexy is

Caused by

A

Similar to Sheehan’s but not specific to women

Intra-Pituitary infarction / haemorrhage

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15
Q

Pituitary apoplexy - there is rapid presentation in

A

patients with pre-existing pituitary tumours which suddenly infarct

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16
Q

A deficiency in a single adenohypophysial hormone results in

A

secondary endocrine gland failure

17
Q

Examples of secondary endocrine gland failure:
o Gonadotrophin ­
o Thyrotrophin
o Corticotrophin

A

-Hypogonadism
-­Hypothyroidism
­‐Hypoadrenocorticalism

18
Q

Signs and symptoms of panhypopituitarism

A

decreased FSH/LH - secondary hypogonadism - secondary amenorrhoea, decreased libido, erectile dysfunction

decreased ACTH - secondary hypoadrenalism - fatigue

decreased TSH - secondary hypothyroidism - fatigue, weight gain

19
Q

Signs and symptoms of Sheehan’s syndrome

A
lethargy
anorexia
weight loss
no lactation
don't resume menses
20
Q

Signs and symptoms of pituitary apoplexy

A

severe sudden headache
bitemporal hemianopia - pressed onto the optic chasm
diplopia
ptosis

21
Q
Hormone replacement therapy and how to check for
ACTH
TSH
Women LH/FSH
Men LH/FSH
GH
A

ACTH - hydrocortisone. Check serum cortisol.

TSH - thyroxine. Check serum free T4.

Women LH/FSH. HRT (E+P). Check by alleviation of symptoms and bleeds

Men LH/FSH. Testosterone. Check by alleviation of symptoms and serum testosterone

GH - GH. Check IGF-1/ growth chart for children.

22
Q

Endocrine causes of short stature

A

Lack of GH (pituitary dwarfism)
Cushing’s
Hypothyroidism
Poorly controlled T1DM

23
Q

Non endocrine causes of short stature

A
genetic - down's, turner's, Prader Willi
Emotional deprivation
Malnutrition/ malabsorption 
systemic disease
Skeletal dysplasia e.g. achondroplasia/ Osteogenesis I
24
Q

Describe the growth axis

A

hypothalamus –> adenohypophysis –> GHRH –> GH –> target tissues / liver –> IGF I –> target tissues

25
Q

Diagnosis of short stature

A

Growth chart of mid parental height

GH provocation test, giving:

  • GHRH and arginine IV
  • insulin IV – hypoglycaemia
  • Glucagon IM
  • Exercise

Measure plasma GH (no response). Low plasma IGF-1

26
Q

whereabouts of the growth axis is affected with:
PW syndrome
Pituitary dwarfism
Laron dwarfism

A

PW — GH deficiency caused by hypothalamus dysfunction

Pituitary dwarfism — childhood lack of GH produced from pituitary

Laron dwarfism — GH receptor defect (on liver) so IGF-I not produced

27
Q

Treatment

A

Somatotrophin given 4/5x per week

28
Q

Signs of GH deficiency in adults

A
increased adiposity 
increased waist:hip ratio
decreased muscle
decreased HDL
increased LDL
decreased psychological wellbeing
29
Q

pros and cons of therapy in adults

A

+ reverse signs + increases bone density

- increased risk of CVS effects - increased soft tissue growth (cardiomegaly) - increased risk of cancer