264. Disorders of the Pituitary Gland Flashcards

1
Q

Hypopituitarism is decreased secretion of anterior pituitary hormones. What are its causes?

A

Hypothalamus: Kallman’s syndrome, tumour, inflammation/infection

Pituitary stalk: trauma, surgery, mass legion, meningioma, carotid artery aneurysm.

Pituitary: tumours, irradiation, inflammation, autoimmunity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the features of hypopituitarism?

A

Very non-specific, tends to effect GH first therefore:

Central obesity, dry wrinkly skin, decreased strength and balance, decreased exercise ability

Will also have the effects of other hormone deficincies e.g. erectile dysfunction, low bp, low glucose, hypothyroid symptoms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are the tests for hypopituitarism?

A

All levels of circulating hormones will be low, dynmaic tests include short synatchen to investigate adrenal axis or insulin tolerance test

MRI scan can be useful to look for a lesion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

How is hypopituitarism treated?

A

hormone replacement, hydrocortisone first for adrenal failure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are the three types of pituitary tumours?

A

Chromophole (70%)

Acidophil

Basophil

Nearly all tumours are benign adenomas

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are the features of a pituitary tumours?

A

Headache, visual field defect

Palsy of cranial nerves III,IV and VI

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

How are pituitary tumours treated?

A

Once assessed by MRI scan they are typically surgically removed typically trans-sphenoidal

Radiotherapy- used for residual or recurrent adenomas

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is pituitary apoplexy?

A

Rapid pituitary enlargement caused by bleed into a tumour. Presents with headaches, blurred vision and reduced GCS.

Urgent steroids and a careful fluid balance is needed to prevent cardiovascular collapse

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

How does hyperprolactinaemia present?

A

woman- menstrual disturbances, galactorrhoea

men- erectile dysfunction, decreased facial hair galactorrhoea

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are the causes of hyperprolactinaemia?

A

Phsyiological- pregancy, breastfeeding, stress

Drugs- metoclopramide, haloperidol, methyldopa, eccies, anti-psychotics.

Diseases- prolactinoma, stalk damage, hypothalmic disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What tests are done to investigate hyperprolactinaemia?

A

Basal PRL

pregnancy test

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

How is hyperprolactinaemia managed?

A

Microprolactinomas <10mm- bromocriptine titrate up. Consider surgery if intolerant

Macroprolactinomas >10mm- treat initially with bromocriptine but consider surgery if pressure symptoms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is acromegaly?

A

Increased growth hormone typically from a pituitary tumour and very rarely from a carcinoid tumour

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are the symptoms of acromegaly?

A

pins and needles in the hands and feet (acroparasthesia)

Reduced libido, increased snorining, headache

“my rings wont fit”, curly hair, was muscle, now fat.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What are the signs of acromegaly?

A

Growth of hands, jaw and feet

Wide nose, big tongue, widely spaced teeth,

Skin darkening, sleep apnoea, goitre, carpal tunnel signs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What complications can those with acromegaly run into?

A

Impaired glucose tolerance
Vascular problems
Neoplasia (colon)
Gigantasisim if occurs before epiphyseal plates fuse

17
Q

What tests are carried out to investigate acromegaly?

A

Glucose, calcium and phosphate increased

Sample growth hormone every 30 mins for 3 hours and then if above 1 then acromegaly confirmed

18
Q

What is the treatment for acromegaly?

A

Excise lesion

somatostatin analogues

If still intolerant GH antagonist

Radiotherapy can be used as adjuvant to surgery

19
Q

What is diabetes insipidus?

What are the two types?

A

Passage of large volumes of urine (>3L) per day due to impaired water reabsorption by the kidneys due to impaired and secretion or impaired kidney responses to ADH

Cranial- lack of ADH
Nephrogenic- imapired response to ADH

20
Q

What are the symptoms?

A

Polyuria, polydyspia, dehydration

symptoms of hypernatraemia (fatigue, muscle twitches)

21
Q

What are the causes of cranial DI?

A

Idiopathic, congenitalm tumour, trauma

Autoimmune, infection

22
Q

What are the causes of nephrgenic DI?

A

Inherited,

Metbolic

Iatrogenic- lithium

Chronic renal disease

23
Q

What tests are done for initial investigation for diabetes insipidus?

A

U&E, calcium, glucose

Serum and urine osmlalilties

24
Q

What is the 8 hour water deprivation test?

A
  1. Fluid deprive for 8 hours
  2. Give desmopressin- drink water
  3. Compare measured samples between the two times
25
Q

How are both types of DI treated?

A

Cranial DI- MRI head, desmopressin

Nephrogenic- Treat the cause, then if not resolved- bendroflumethiazide

26
Q

How can diabetes insipidus become an emergency?

A

Severe hypernatraemia

Needs to lower sodium slowly

Desmopressin as therapeutic trial

27
Q

What is SIADH?

A

syndrome of inappropriate ADH secretion. ADH secreted despite low plasma osmolality

Causes strong urine, low plasma osmolality and hyponatraemia