Adrenal and Pituitary Disease Lecture Flashcards

1
Q

What are the symptoms and signs that may make you suspect hypoadrenalism?

A
  • Weight loss and lethargy
  • Postural hypotension
  • Nausea, vomiting
  • Hyponatraemia +/- hyperkalaemia
  • Addisonian crisis
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2
Q

What are some symptoms/signs of Addison’s Disease?

A
  • Mucous membrane pigmentation
  • Skin pigmentation (extensors, knuckles esp)
  • Freckling
  • Vertigo
  • Pigment accentuation at nipples
  • Pigment concentration in skin creases or scars
  • Weight loss
  • Anorexia
  • Vomiting + diarrhoea
  • Muscular weakness
  • Postural hypotension
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3
Q

Why do you have changes to pigmentation in addison’s disease?

A

Increased ACTH causes increases melanocyte stimulating hormone

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4
Q

What are the clinical findings of an adrenal crisis?

A
  • Dehydration, hypotension or shock out of proportion to illness
  • N + V
  • Weight loss
  • Acute abdomen
  • Unexplained hypogycaemia
  • Unexplained fever
  • Hyponatraemia, Hyperkalaemia, hypercalcaemia, eosinophilia, azotemia (urea + creatinine)
  • Hyperpigmentation or vitiligo
  • Other AI issues
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5
Q

What should low sodium and high potassium always make you think of?

A

Primary hyperadrenalism

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6
Q

What investigations should you do for hypoadrenalism?

A

Serum cortisol level: (random vs morning)
- Pulsatile secretion and diurnal variation makes interpretation difficult
- Time of day dependent
- Wide reference range (for morning cortisol level)

Stimulation testing:
- Short synacthen test (serum cortisol O’, 30’ and 60’ after synthetic ACTH 260 IM)

If patients are on exogenous glucocorticoids you can just diagnose clinically

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7
Q

How can you differentiate primary adrenal insufficiency from secondary or tertiary adrenal insufficiency?

A

The Synacthen Test/ACTH Stimulation Test
- ACTH should increase cortisol

If low cortisol = primary problem
Normal or increased cortisol= secondary or tertiary problem

Check plasma ACTH also

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8
Q

What other deficiencies should you investigate when you suspect PRIMARY adrenal insufficiency?

A

Mineralocorticoid deficiency!
- Hyperkalaemia
- Aldosterone and renin

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9
Q

What antibodies should you check for if someone has PRIMARY adrenal insufficiency?

A

Adrenal
Ovarian
Thyroid

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10
Q

How quickly can you withdraw glucocorticoids safely?

A

You can get clinically significant suppression after 2 weeks of glucocorticoids over supraphysiological doses

Reduce gradually!! Esp once at 7.5mg/day of pred

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11
Q

If someone with Addison’s disease is admitted with appendicitis- what should you consider in the management of them?

A

IMMEDIATE: the acute stress of the illness means they probs need more help
- IV hydration
- IV hydrocortisone 100mg
- When tolerating oral intake, commence on oral replacement and then taper down

LONG TERM:
- Need to be monitored to ensure replacement was enough
- Weight
- Cushingoid features
- Electrolytes

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12
Q

If someone presents with hypopituitarism presents with an acute illness what are your management priorities?

A
  • Glucocorticoid assessment and replacement (IMPORTANT- this is life threatening so should be immediate)
  • Then give thyroxine after
  • Others (but not life threatening): gonadal hormones, growth hormone in children
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13
Q

What are the features of cushing’s syndrome?

A
  • Depression/psychoses
  • Mood alterations
  • Cataracts
  • Moon face
  • Hirsutism
  • HTN with secondary cardiomegaly
  • Elevated glucose
  • Muscle weakness
  • Osteoporosis
  • Thin skin
  • Proximal myopathy
  • Oligomenorrhea/amenorrhea
  • Abdominal striae
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14
Q

What are some causes of Cushing’s?

A

ACTH Dependent Cushing’s Syndrome:
- Cushing disease
- Ectopic ACTH syndrome
- Ectopic CRH syndrome

ACTH Independent Cushing’s Syndrome:
- Adrenal adenoma
- Adrenal carcinoma
- Micro/Macronodular hyperplasia

Pseudo-Cushing’s Syndrome:
- MDD
- Alcoholism

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15
Q

How do you diagnose Cushing’s?

A

First:
- Increased urinary free cortisol (3 24hr collections)
- Lack of cortisol suppression after low-dose dexamethasone testing
- Increase Late evening salivary cortisol

Then: consider the ACTH vs not ACTH causes
- ACTH
- CRH test
- 8mg dex
- CT/MRI adrenal
- MRI pituitary
- BIPSS

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16
Q

What can cause false positives from the low dose dexamethasone suppression test (DST)?

A
  • Increased oestrogen
  • Decreased dexamethasone
  • Drugs which increase hepatic metabolism of it: barbiturates, phenytoin
  • Depression, alcoholism, chronic anxiety
17
Q

What are some causes of secondary HTN?

A
  • Renovascular disease
  • Primary renal disease
  • Oral contraceptives
  • Phaeochromocytoma
  • Cushing’s Syndrome
  • Primary Aldosteronism
  • OSA
  • Coarctation of the aorta
  • Hypothyroidism
  • Primary hyperparathyroidism
18
Q

What are some initial screening tests for the endocrine causes of secondary HTN?

A

Plasma metanephrines (fasting)

Aldosterone renin ratio:
- Hard to interpret if pt on anti-hypertensives
- Primary mineralocorticoid excess: renin suppressed, ratio up
- Secondary mineralocorticoid excess: renin increased (like renal artery stenosis), ratio down

Screening for hypercortisolism

19
Q

What are some causes for a unilateral adrenal mass?

A

HORMONE EXCESS:
Adenoma
ACC
Pheochromocytoma
Adrenal hyperplasia

NO HORMONE EXCESS:
Adenoma
Myolipoma
Neuroblastoma
ACC
Metastasis
Cyst

20
Q

What should you consider when investigating an adrenal mass?

A

SIZE:
- >3.5-4cm: may need surgery as difficult to exclude malignancy (can’t biopsy incase malignancy)
- Imaging can help as adenomas are lipid rich on imaging

HORMONAL ACTIVITY:
- Catecholamines important

21
Q

What hormones are made by the adrenal gland?

A
22
Q

What is the triad of phaeochromocytomas?

A

Headache
Sweating
Palpitations

23
Q

How do you screen for a phaeochromocytoma?

A

Plasma metanephrines (fasting)

24
Q

What are paragangliomas?

A

Extra-adrenal tumours
Genetic link with phaeochromocytoma

25
Q

DDx of a large pituitary mass

A

BENIGN:
- Pituitary adenoma
- Meningioma
- Craniopharyngioma

PITUITARY HYPERPLASIA:
- Lactotroph hyperplasia (during pregnancy)

MALIGNANT:
- there’s a million I cbf typing

CYST

ABSCESS

26
Q

What is the investigative approach to a pituitary mass?

A
  • Assess and treat secondary hyperadrenalism (priority!!)
  • Imaging: MRI is great

Biochemical:
- Pituitary hypofunction: secondary hypoadrenalism, hypothyroidism, hypogonadism
- Pituitary hyperfunction: prolactinoma, acromegaly, Cushing’s

27
Q

Investigations for pituitary hypofunction:

A

Cortisol
T4
Male: testosterone, SHBG, FSH, LH
Female: oestradiol, progesterone, FSH, LH

28
Q

What is pituitary hormonal replacement?

A

Glucocorticoid:
- Hydrocortisone

Thyroxine

Gonadal hormones:
- Testosterone
- Oestrogen

Growth hormone

ADH/Vasopressin

29
Q

What can hyperprolactinaemia do?

A

Cause hypogonadotrophic hypogonadism

30
Q

What causes hyperprolactinaemia?

A
  • Prolactin secreting adenoma (prolactinoma)
  • Dopamine antagonism (metoclopramide, anti-depressants)
  • Renal failure
  • Pregnancy
31
Q

What are some symptoms/complications of prolactinomas?

A

Mass effect: headaches, visual field defect (bitemporal hemianopia)
Hypopituitarism

32
Q

What are prolactinomas really sensitive to?

A

Dopamine agonists so might not even need surgery