Endocrinology Flashcards

1
Q

Addison’s treatment

A

Hydrocortisone, Fludrocortisone combo

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2
Q

Addison’s pathology

A

autoimmune adrenal gland destruction = reduced cortisol & aldosterone production
low Na, glucose, calcium
high K

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3
Q

Addison’s investigations

A

ACTH stimulation test
9am serum/salivary cortisol = usually low, should be high
Short synACTHen test - exclude Addisons if high

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4
Q

Addisonian crisis

A
  • acute exacerbation of chronic insufficiency
  • adrenal haemorrhage WF syndrome
  • steroid withdrawal
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5
Q

Addisonian crisis management

A

100mg hydrocortisone IM/IV
1L saline 30-60 mins
infused w dextrose if needed
no fludrocortisone

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6
Q

Addison’s symptoms

A

lethargy, weak, anorexia, N, V, weight loss, salt craving, hyperpigmentation, vitiligo, loss of pubic hair, hypotension

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7
Q

Addisonian crisis symptoms

A

collapse
shock, pyrexia
hypoglycaemic

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8
Q

Cushing’s pathology

A

chronic glucocorticoid excess = too much cortisol

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9
Q

Cushing’s features

A

proximal myopathy, striae, bruising, osteoporosis, DM, obesity,
HTN
hypokalaemia

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10
Q

Cushing’s appearance

A

moon face, acne, hirsutism, fat pads, striae, thin limbs, bruising, thin skin

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11
Q

Cushing’s causes

A

iatrogenic steroids
adrenal adenoma/carcinoma/hyperplasia
cushings disease
ectopic ACTH secretion

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12
Q

Cushing’s disease

A

pituitary adenoma > ACTH secretion > bilateral adrenal hyperplasia

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13
Q

High dose dex suppression

Cushing’s syndrome

A

Cortisol not suppressed

ACTH suppressed

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14
Q

High dose dex suppression

Cushing’s disease

A

Cortisol & ACTH suppressed

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15
Q

High dose dex suppression

Ectopic ACTH

A

Cortisol & ACTH NOT suppressed

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16
Q

How to treat Cushing’s

A

Disease = trans-sphenoidal excision
Adrenal adenoma/carcinoma = adrenelectomy
Ectopic ACTH = tumour excision, metyrapone

17
Q

Primary hyperaldosteronism?

A

excess aldosterone independent of RAAS
Hypokalaemia - weak, hypotonia, hyporeflexia, cramps
Paraesthesia
HTN

18
Q

Causes of primary hyperaldosteronism

A

Bilateral adrenal hyperplasia 70%

Adrenocortical adenoma 30% = Conn’s syndrome

19
Q

Primary hyperaldosteronism investigations

A

mixed Na,
low K
alkalosis

Aldosterone renin ratio = increased

ECG - flat/inverted T waves, U waves, depressed ST
segments, prolonged PR and QT intervals

Adrenal CT/MRI

20
Q

Primary hyperaldosteronism mgmt?

A

Conn’s: laparoscopic adrenelectomy

Hyperplasia: spironolactone, eplerenone, amiloride

21
Q

Secondary hyperaldosteronism?

A

Increased renin from decreased renal perfusion

Diuretics, CCF, hepatic failure, nephrotic syndrome

22
Q

Secondary hyperaldosteronism investigation

A

Aldosterone renin ratio = normal

23
Q

Phaeochromocytoma

A

Catecholamine-producing tumours (adreneline)
sympathetic paraganglia
adrenal medulla/aortic bifurcation
(MEN2a, 2b assoc)

24
Q

Phaeochromocytoma presentation

A

Triad:
episodic headache
sweating
tachycardia

lots fo adrenergic features

25
Q

Phaeochromocytoma investigations

A

Plasma + urine metadrenaline & vanillylmandellic acid

MIBG scan

26
Q

Phaeochromocytoma mgmt?

A

Chemo, radiolabelled MIGB
Surgery - adrenelectomy
A & B blockers prep

27
Q

Hypertensive crisis

A

Pallor
Pulsating headache Impending doom
↑↑BP
Cardiogenic shock (ST elevation)

28
Q

Hypertensive crisis mgmt?

A
  • Phentolamine 2-5mg IV α-blocker
  • Labetalol 50mg IV
  • until dBP <110
  • phenoxybenaime to maintain
  • surgery too