Pituitary Disease Flashcards

1
Q

What level of prolactin raises suspicion of a prolactin-secreting tumour being present?

A

> 5000

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2
Q

How are prolactinomas treated medically?

A

Cabergoline (a dopamine agonist)

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3
Q

What are known side-effects of dopamine agonists?

A

Nausea
Vomiting
Depression

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4
Q

What causes acromegaly?

A

Excess growth hormone secretion

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5
Q

Why would onset of excess GH in childhood cause gigantism, but not when starting in adults?

A

As in children epiphyseal fusion has not yet occurred.

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6
Q

What pathology occurs in acromegaly?

A

Thickening of the soft tissue - most will die due to heart failure.

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7
Q

What is the most common cause of acromegaly?

A

Pituitary adenoma

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8
Q

How is acromegaly treated?

A

Surgical removal of the adenoma.

If not suitable, give loreotide (a synthetic somatostatin). This will cause tumour shrinkage. Dopamine agonists can also be effective.

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9
Q

What should acromegaly patients be screened for?

A

Bowel cancers (as increased risk of polyps)
Signs of CVD
Sleep apnoea (if present give CPAP)

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10
Q

What is the issue in Cushing’s syndrome?

A

Excess cortisol production

Results in protein loss, myopathy, osteoporosis, and thinning of the skin.

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11
Q

What mental health act impacts can Cushing’s syndrome have?

A

Psychosis
Depression

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12
Q

What are the key features of Cushing’s syndrome?

A

Thin skin
Proximal myopathy
Osteoporosis

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13
Q

How is Cushing’s syndrome tested for?

A

High-dose dexamethasone suppression test

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14
Q

What is the difference between Cushing’s disease and Cushing’s syndrome?

A

Cushing’s disease involves the pituitary only, whereas Cushing’s syndrome is pathology elsewhere in the body.

Critically, both produce the same symptoms.

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15
Q

What is the most common cause of Cushing’s?

A

Pituitary disease

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16
Q

What are common causes of Cushing’s syndrome?

A

Adrenal tumour
Ectopic ACTH from thymus/lungs/pancreas

17
Q

What are symptoms of hypopituitarism?

A

Amenorrhoea
Infertility
Impotence
Loss of facial hair
Gynaecomastia
Obesity

18
Q

What are potential causes of hypopituitarism?

A

Surgery
Granulomatous disease (e.g. sarcoidosis)
Autoimmune (e.g. Sheehan’s syndrome)

19
Q

How is hypopituitarism managed?

A

Thyroxine
Hydrocortisone
ADH
GH
HRT/Testosterone (gender-dependent)

20
Q

What is a potential complication of testosterone therapy?

A

Polycythaemia (which increases risk of stroke/MI)

21
Q

What pathology should be screened for in those about to initiate testosterone therapy?

A

Prostate cancer - as therapy can cause enlargement of the gland.

22
Q

What test is used to investigate diabetes insipidus?

A

Water deprivation test

23
Q

How is cranial DI differentiated from nephrogenic DI?

A

In cranial DI, desmopressin (synthetic ADH) injection will cause an increase in osmolarity to normal levels.

However, in nephrogenic DI there will not be a response to desmopressin.

24
Q
A