Adrenals Flashcards

1
Q

What is produced in the Zona Glomerulosa (Cortex)?

A

Mineralocorticoids

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2
Q

What is produced in the Zona Fasciculata (Cortex)?

A

Glucocorticoids

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3
Q

What is produced in the Zona Reticularis (Cortex)?

A

Sex Steroids

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4
Q

What is produced in the Adrenal Medulla?

A

Adrenaline

Noradrenaline

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5
Q

What is Primary Hyperaldosteronism?

A

Autonomous aldosterone overproduction from the Adrenal Gland, leading to subsequent suppression of Plasma Renin Activity.

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6
Q

What are the main causes of Primary Hyperaldosteronism?

A

Adrenal Adenoma - Conn’s

Bilateral Adrenal Cortex Hyperplasia

Familial

Rarely Aldosterone producing Adrenal Carcinoma

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7
Q

How does Primary Hyperaldosteronism typically present?

A

Difficult to control HTN

Hypokalaemia signs

Mood Disturbance, headaches, tiredness

Polyuria, Nocturia

Muscle weakness, Paraesthesia

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8
Q

How would you investigate a possible case of Primary Hyperaldosteronism?

A

Hypokalaemia

Potassium in the urine

High levels of aldosterone & Aldosterone:Renin ratio

Fludrocortisone Suppression Test

Postural Test

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9
Q

How would you manage an Adrenal Adenoma?

A

Adrenalectomy (Laparoscopic)

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10
Q

How woud you manage Bilarteral Adrenal Hyperplasia?

A

Spironolactone

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11
Q

What is Cushing’s Syndrome?

A

Syndrome associated with a chronic inappropriate elevation of free circulating Cortisol.

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12
Q

What are the main causes of Cushing’s?

A

Exogenous - Steroid Exposure

Endogenous - ACTH Dependent (Pituitary Adenoma, Lung tumour etc)

ACTH Independent (Benign Adrenal Adenoma, hyperplasia, carcinoma)

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13
Q

How does Cushing’s Syndrome present?

A

Moon Face

Interscapular Fat Pad

Central Obesity

Purple Striae

HTN

Ankle Oedema

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14
Q

How would you investigate a suspected case of Cushing’s?

A

Only for patients with a high pre-test probability:

24hr Urinary Free Cortisol

Overnight Dexamethasone Suppression Test

Low-dose Dexamethasone Suppression Test

Morning Cortisol >50 nanomol/L

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15
Q

How should you manage a confirmed case of Cushing’s Syndrome?

A

Discontinue Steroids

Metyrapone/Ketoconazole

Surgical

Trans-sphenoidal Resection for Pituitary Adenoma

Radiotherapy if persistent post-op

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16
Q

What are the main complications of Cushing’s Syndrome?

A

Diabetes

Osteoporosis

Hypertension

Infections

17
Q

What is a Phaeochromocytoma?

A

Tumour of the Catecholamine-producing Chromaffin cells of the Adrenal Medulla.

18
Q

How does a patient with a Phaeochromocytoma typically present?

A

Paroxysmal attacks of

Palpitations

Headaches

Episodic Sweating

Anxiety

Nausea

Chest Pain

19
Q

What are the main risk factors for the development of a phaeochromocytoma?

A
20
Q

How would you investigate a suspected case of Phaeochromocytoma?

A

24 Hr Urine Collection - to check for catecholamines

Plasma free metanephrines

Genetic Testing

CT

21
Q

What are the main causes of Adrenal Insufficiency?

A

Addison’s (Primary)

Pituitary or Hypothalamic Disease (Secondary)

22
Q

What are the main symptoms of Adrenal Insufficiency?

A

Fatigue, Weakness, Myalgia

Weight Loss

Diarrhoea + Vomiting

Abdominal Pain

Depression

Increased Pigmentation

Postural Hypotension

Loss of Body hair in women

23
Q

How does an Addinsonian Crisis present?

A

Vomiting, Diarrhoea, Abdo Pain

Shock

24
Q

How should you investigate the cause of Adrenal Insufficiency?

A

Short SynACTHen Test (<550 nmol/L at 30 mins)

25
Q

How should you manage an Addinsonian Crisis?

A

Rapid IV Fluid rehydration

50ml 50% Dextrose

Hydrocortisone IV Bolus

Treat the Cause & Monitor

26
Q

How do you treat Chronic Adrenal Insufficiency?

A

Replace Deficits

GCs with Hydrocortisone

MCs with Fludrocortisone

In times of stress (ie. Illness), increase dose to mimic physiological reaction.

27
Q

What are the main complications of Adrenal Insufficiency?

A

Hyperkalaemia

Death (Crisis)

28
Q

What are the main causes of Hyperkalaemia?

A

Renal Disease - HTN, DM

Low RAAS Activity - ACE-i, ARBs,

Systemic K+ Release - Rhabdomyolysis, DKA

DCT Damage

Spurious Sample (If exceedingly high + very low Ca)

29
Q

How do you manage Hyperkalaemia?

A

10 10 10 50 50

10ml 10% Calcium Gluconate

10U Actrapid

50ml 50% Glucose

Nebulised SABA

12 Lead ECG

30
Q

What are the main causes of Hypokalaemia?

A

GI Loss - Vomiting, Diarrhoea

Redistribution into cells

Renal Loss

Decreases Intake

31
Q

How should you manage a case of Hypokalaemia?

A

Always correct Magnesium

3.0-3.5 - Oral KCl + Recheck

<3.0 - IV KCl

32
Q

What is Polycystic Ovary Syndrome?

A

Syndrome defined by the presence of:

Hyperandrogenism (Hirtusim, ACNE)

Oligo/Amenorrhoea

Polycystic Ovaries on USS

33
Q

What are the main symptoms of PCOS?

A

Hair Loss

Hirtuism

Pelvic Pain

Infertility

Oligomenorrhoea

Fatigue

ACNE

34
Q

How would you investigate a suspected case of PCOS?

A

High LH, LH:FSH Ratio

High Androgens

Low ‘Sex-hormone binding globulin;.

Transvaginal USS for increased ovarian follicles