Pituitary disorders Flashcards

1
Q

What are the usual clinical presentation of pituitary tumours?

A
  • Visual loss = pressure on optic chiasm

- Headache = lateral growth of the tumour

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2
Q

What are biochemical assessments of pituitary disease?

A
  • Thyroid axis = TSH
  • Gonadal axis = LH + FSH
  • Prolactin axis = Serum prolactin
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3
Q

What are the dynamic assessments of HPA and GH axes?

A

Stimulation test = suspected hormone deficiency
Suppression test = suspected hormone excess

Adrenal axis

  • Deficiency = stimulate adrenals by ACTH
  • Excess = suppress ACTH with steroids

GH axis

  • Deficiency = response to hypoglycamic stress
  • Excess = suppress GH axis with glucose load
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4
Q

What is prolactinoma?

A

Prolactin-secreting pituitary tumour

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5
Q

What are the symptoms of hyperprolactinaemia in women?

A
  • Menstrual disturbance
  • Fertility problems
  • Galactorrhea
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6
Q

What are the symptoms of hyperprolactinaemia in men?

A

-Visual loss
-Lactation
-Erectile dysfunction
-Infertility
(usually present later than females)

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7
Q

What is prolactin disinhibition and what is its importance?

A
  • Blocking of the stalk as prolactin is under tonic inhibition by dopamine
  • Prolactinomas are treated medically while non-functioning pituitary tumours are treated surgically
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8
Q

How are prolactinomas treated?

A
  • Dopamine agonists

- Bromocriptine or Cabergoline (reduces prolactin)

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9
Q

What is non-functioning pituitary adenoma?

A

Pituitary tumour that leads to no secretion of biologically active hormones

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10
Q

What are the clinical features of NFPA?

A
  • Low testosterone
  • Growth failure in children
  • Menstrual cycle loss
  • Infertility
  • Loss of sex drive
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11
Q

Treatment for NFPA?

A

Surgery

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12
Q

What is acromegaly?

A

GH-secreting pituitary tumour that leads to large extremities (large hands and feet)

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13
Q

What are long term complications of acromegaly if untreated?

A
  • Premature cardiovascular death
  • Disfiguring body changes
  • Hypertension
  • Diabetes
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14
Q

What is the treatment for acromegaly?

A
  • Surgical removal of tumour
  • Dopamine agonist (reduce GH secretion)
  • Somatostatin analogues (reduce GH secretion)
  • Block GH receptor (e.g. pegvisomant)
  • Radiotherapy
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15
Q

What is cushing’s disease

A

ACTH-secreting tumour

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16
Q

What are the clinical changes in appearance in cushing’s disease?

A
  • Round pink face
  • Round abdomen
  • Thin skin (easy bruising)
  • Red stretch marks on abdomen
17
Q

What is the treatment for cushing’s disease?

A
  • Surgery
  • Radiotherapy
  • Medication to reduce effect of cortisol (e.g. ketoconazole, mitotane)
18
Q

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

A

Cushing’s disease = due to tumour

Cushing’s syndrome = may be due to other pathologies (e.g. ectopic ACTH, steroid medication)

19
Q

What is Diabetes insipidus?

A

Large quantities of pale (insipid) urine

20
Q

How does Diabetes insipidus present?

A

-extreme thirst (polydipsia)

21
Q

What is the difference between cranial DI and nephrogenic DI?

A
  • Cranial DI is vasopressin deficiency pituitary disease

- Nephrogenic DI is vasopressin resistance kidney disease

22
Q

What are the consequences of untreated DI?

A
  • Severe dehydration
  • Hypernatraemia
  • Reduced consciousness
  • Coma
  • Death
23
Q

What is the treatment for cranial DI?

A

Synthetic vasopressin (Desmopressin)

24
Q

What is pituitary apoplexy?

A

A sudden vascular event in pituitary tumour (stroke) -> haemorrhage and/or infarction

25
Q

How does pituitary apoplexy clinically present?

A
  • Sudden onset headache
  • Double vision
  • Cranial nerve palsy