Hyposecretion of anterior pituitary hormones Flashcards

(45 cards)

1
Q

What is primary endocrine gland disease?

A

When it caused by disorder of the endocrine gland

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2
Q

What is secondary endocrine gland disease?

A

When it is caused by disorder of the anterior pituitary

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3
Q

What is tertiary endocrine gland disease?

A

When it is caused by disorder of the hypothalamus

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4
Q

What is panhypopituitarism?

A

Decreased production of all anterior pituitary hormones

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5
Q

How can panhypopituitarism be acquired? (6)

A
Tumours- hypothalamic and pituitary
Radiation- damage
Infection- meningitis
Traumatic brain injury
Infiltrative disease
Inflammatory
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6
Q

How else can panhypopituitarism be caused?

A

Congenital (rare) or mutations (very rare)

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7
Q

How does panhypopituitarism usually develop?

A

In an adult with progressive loss of pituitary secretion>

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8
Q

What is the normal order of pituitary secretion loss?

A

Gonadotrophins
GH
Thyrotrophin
Corticotrophin

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9
Q

What are the three main types of panhypopituitarism?

A

Simmond’s disease
Sheehan’s syndrome
Pituitary apoplexy

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10
Q

What is the onset of Simmond’s like?

A

Insidious- very slow

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11
Q

What are the causes of Simmond’s? (5)

A
Infiltrative processes
Pituitary adenomas
Craniopharyngiomas
Cranial injury
Post surgery
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12
Q

What are the symptoms of Simmond’s mainly due to?

A

Loss of thyroidal, gonadal and adrenal function

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13
Q

What are the symptoms of Simmond’s?

A
Secondary amenorrhoea
Impotence
Loss of libido
Tiredness
Waxy skin
Loss of body hair
Hypotension
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14
Q

What is different about Sheehan’s compared to the other two?

A

It is specific to women

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15
Q

How does Sheehan’s develop?

A

Develops acutely following postpartum haemorrhage resulting in pituitary infarction

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16
Q

How does the postpartum haemorrhage lead to pituitary infarction?

A

The blood loss results in vasoconstrictor spasm of the hypophysial arteries and this leads to ischaemia and necrosis of the pituitary

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17
Q

How does Sheehans and pituitary apoplexy compare?

A

Very similar but pituitary apoplexy is in men and women and just due to normal haemorrhages

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18
Q

How do you diagnose hypopituitarism?

A

You can’t measure hypothalamic hormones so you measure basal values of the plasma for pituitary or target endocrine gland hormones

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19
Q

Why will a single measurement not suffice?

A

Hypothalamic hormones are released in pulses

20
Q

What test can you use to find out if a person is producing hormones at a normal level?

A

Stimulation test

21
Q

What does a lack of somatotrophin cause in children and adults?

A

Pituitary dwarfism in children

Effects uncertain in adults

22
Q

What are other causes of short stature in children? (6)

A
Genetic- Down's, Turner's, Prader Willi
Malnutrition
Emotional deprivation
Systemic disease
Malabsorption
Endocrine disorders- Cushing's, hypothyroidism, GH deficiency
23
Q

What are the acquired causes of GH deficiency in children? (6)

A
Tumours of the hypothalamus or pituitary
Other intercranial tumours nearby (optic nerve glioma)
Irradiation
Head injury
Infection or inflammation
Severe psychosocial deprivation
24
Q

What are the genetic causes of GH deficiency in children?

A

Congenital (rare) - Deficiency of hypothalamic GHRH
Mutations of the GH gene (very rare)
Developmental abnormalities

25
What controls GH at a hypothalamic level?
GHRH and somatostatin
26
What are most endocrine-related causes of short stature due to?
Decreased production of GHRH
27
What does GH stimulate the production of in the liver?
IGF-1 (insulin like growth factor) (liver is main source but is produced in many places)
28
What does IGF-1 do?
Mediate growth effects
29
What is laron dwarfism due to?
GH receptor defect
30
Explain how GH receptor defect leads to Laron dwarfism?
As a result IGF-1 levels are low as somatotrophin isn't having an effect
31
What is the main presentation of Kallmann's syndrome?
Hypogonadism and anosmia
32
What is Kallmann's caused by?
Genetic defect where the neurones in the embryo that will go on to produce GnRH are unable to migrate to the hypothalamus so their hypothalamus lacks GnRH neurones
33
What other condition leads to hypogonadism and is a hypothalamic defect?
Prader Willi
34
What is the standard way of testing the ability of the pituitary to produce GH?
Stimulate GH production by inducing hypoglycaemia (The gold standard is insulin induced hypoglycaemia)
35
What is the main aim of pituitary deficiency treatment?
Restore homeostasis by replacing missing hormones
36
What does growth hormone therapy lead to in children?
Acceleration of linear growth | Decreased body fat
37
Which children respond better to growth hormone therapy?
Young and obese
38
What is a common problem with GH therapy?
They develop resistance (antibodies)
39
How is growth hormone therapy administered?
Subcutaneous or intramuscular
40
When is GH administered?
Daily- In the afternoon as levels are normally high at night anyway
41
What is the half life of GH like?
Short- 20 mins
42
What does GH work on hence what is its action duration like?
Protein synthesis so long
43
What are the adverse effects of GH?
Lipoatrophy at site of injection Intracranial hypertension- headaches Increased risk of cancer
44
What are the signs and symptoms of GH deficiency in adults?
``` Reduced lean mass Increased adiposity Increased waist:hip ratio Reduced muscle strength and bulk Decreased HDL and increased LDL Impaired psychological wellbeing ```
45
What are the 4 ways of diagnosing GH deficiency in adults?
Lack of response to GH stimulation test GHRH and Arginine Low plasma IGF-1 Low plasma IGF-BP3