Pituitary Disease Flashcards

1
Q

How are benign adenomas categorised based on size?

A

Microadenoma < 1 cm

Macroadenoma > 1 cm

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2
Q

What are the 6 hormones released from the anterior pituitary?

A
  • ACTH
  • FSH
  • GH
  • LH
  • Prolactin
  • TSH

Release of these hormones is controlled by the hypothalamus

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3
Q

What are the two hormones released from the posterior pituitary?

A

ADH

Oxytocin

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4
Q

How can the clinical features of pituitary adenomas categorised?

A
  • Mass effects (visual disturbances and headaches)

- Endocrine effects (symptoms relate to the hormone which is in excess)

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5
Q

What are the different types of pituitary adenomas?

A
  • Prolactinoma
  • ACTH secreting adenoma (presents as Cushings)
  • GH secreting adenoma (presents as acromegaly)
  • FSH+LH secreting adenoma
  • TSH secreting adenoma
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6
Q

What is Prolactinoma?

A
  • Excess prolactin release due to adenoma
  • Prolactin release from anterior pituitary is usually inhibited by dopamine release from the hypothalamus
  • Clinical presentation depends on age and gender
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7
Q

What is the clinical presentation of Prolactinoma?

A

=> For women of reproductive age:

  • Oligomenorrhoea
  • Galactorrhoea

=> For men and post menopausal women:

  • Erectile dysfunction
  • Reduced facial hair
  • Galactorrhoea
  • Osteoperosis
  • Headaches and visual disturbances
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8
Q

What are the causes of hyperprolactinaemia?

A
  • Adenomas (Prolactinoma)
  • Pregnancy
  • Oestrogens
  • Stress
  • Acromegaly
  • Primary hypoparathyroidism
  • PCOS
  • Compression of pituitary stalk causing disinhibition of prolactin
  • Drugs (dopamine antagonists, SSRIs, phenothiazines)
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9
Q

What are the investigations is suspected Prolactinoma?

A
  • Prolactin levels (First line)
  • Pregnancy tests
  • Blood tests (TFTs, U&Es)
  • MRI (to determine location and size) Gold standard
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10
Q

What is the management Prolactinoma?

A

=> Medical - Dopamine agonists:
BROMOCRIPTINE, CABERGOLINE

=> Surgery to resect adenoma in cases of failed medical therapy

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11
Q

What is involved in the normal secretion of GH?

A
  • GHRH released from hypothalamus acts on anterior pituitary
  • Anterior pituitary releases GH which acts on liver
  • Liver releases IGF-1
  • Increased secretion of GH presents as acromegaly

Excess secretion of GH leads to acromegaly

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12
Q

What is the clinical presentation of Acromegaly?

A
  • Big hands, face and jaw
  • Coarse face
  • Big tongue
  • Wide space between teeth
  • Puffy lips, eye lids and skin
  • Dark skin
  • Carpal tunnel signs
  • Increased sweating
  • Headache, backache
  • Visual field defects
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13
Q

What are the complications of acromegaly?

A
  • Hypertension
  • Heart failure (LV hypertrophy)
  • Obstructive sleep apnoea
  • Cardiomyopathy
  • Carpal tunnel syndrome
  • Proximal myopathy
  • Colorectal cancer
  • Panhypopituitarism
  • Resistance to insulin (therefore can cause diabetes)
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14
Q

What are the investigations in suspected acromegaly?

A

=> Bloods
- IGF-1 is first line investigation

=> OGTT

=> Pituitary MRI

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15
Q

What is the management of acromegaly?

A

=> Surgery (1st line) - as acromegaly can causes structural heart problems

=> If surgery fails: somatostatin analogues (GHIH) - eg Octreotide

=> If GHIH fails, then GH antagonists (Pegvisomant) or radiotherapy

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16
Q

In what order are hormones affected in hypopituitarism?

A
  • GH
  • FSH/LH
  • Prolactin
  • TSH
  • ACTH
17
Q

What are the causes of hypopituitarism?

A

=> If the problem concerns the hypothalamus:

  • Kallmans syndrome
  • Tumour
  • Inflammation
  • Infection

=> Pituitary stalk:

  • Trauma
  • Surgery
  • Mass lesion

=> Pituitary:

  • Tumour
  • Radiation
  • Inflammation
  • Autoimmunity
18
Q

What are the clinical features of hypopituitarism?

A

=> GH lack:

  • Central obesity
  • Atherosclerosis
  • Dry skin

=> FSH/LH lack:

  • Decreased fertility
  • Reduced libido
  • Erectile dysfunction

=> Prolactin lack:
- Cannot lactate

19
Q

What is Diabetes Insipidus?

A
  • Decreased ADH secretion
20
Q

What are the causes of DI?

A
  • Caused by defect of pituitary gland (cranial) or defect in kidney (nephrogenic)

=> Causes of Cranial DI:

  • Idiopathic
  • Post head injury
  • Pituitary surgery
  • Craniopharyngiomas
  • Wolfram’s syndrome
  • Haemochromatosis

=> Causes of Nephrogenic DI:

  • Genetic
  • Drugs
  • Tubulo interstitial disease
  • Electrolytes
21
Q

What are the clinical features of DI?

A
  • Polyuria
  • Polydypsia
  • Dehydration
  • Hypernatremia
22
Q

What are the investigations in suspected DI?

A

=> Measure urine output

=> Plasma osmalality, urine osmalality
- High plasma osmolality and low urine osmolality

=> 8 hour deprivation test

23
Q

What is the management of DI?

A

=> Central DI:
- Synthetic analogue of ADH = Desmopressin

=> Nephrogenic DI:

  • Thiazides (gets rid of built up electrolytes)
  • Low salt/protein diet