Endocrinology Flashcards

1
Q

MEN syndromes

A

MEN I (3 Ps) – Pituitary, Parathyroid, Pancreas

MEN IIa (1M,2Ps) – Medullary Thyroid Carcinoma, Pheochromocytoma, Parathyroid

  • OR “I am meant to sit in an AC room” – 3Cs Calcium, Calcitonin, Catecholamines

MEN IIb (2Ms,1P) – Medullary Thyroid Carcinoma, Marfanoid habitus/mucosal neuroma, Pheochromocytoma

  • Every man wants to be a Pharaoh with Medium Cars on Mars with New Romans”
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2
Q

Management of Hypoglycaemia

A
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3
Q

Whipple’s triad

A
  1. Plasma hypoglycaemia
  2. Symptoms due to low blood glucose
  3. Resolution of symptoms with correction of hypoglycaemia
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4
Q

Known hypopituitarism –> Gradual onset

Pituitary apoplexy sudden onset

Panhypopituitarism

Reduced GCS

Hypotension

Hypoglycaemia

Diagnosis? Tx?

A

Hypopituitary coma

  • URGENT IV Hydrocortisone
  • Then, T3 replacement
  • Then treat underlying cause
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5
Q

Simmond’s disease

vs

Sheehan’s syndrome

vs

Pituitary apoplexy

A
  • Simmond’s disease
    • Insidious onset
    • Hypopituitarism
  • Sheehan’s syndrome
    • Women
    • PPH
    • Sudden onset
    • Hypopituitarism
  • Pituitary apoplexy
    • Pre-existing pitutiary adenoma –> acute infarction
    • Rapid onset
    • Headache
    • Xanthochroma
    • Hypopituitarism
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6
Q

Ix for GH deficiency

Tx

A

Insulin (hypoglycaemia is a potent stimulus for GH release)

Normal = GH release

Pituitary dwarfism –> no GH release

Tx: Somatotropin (recombinant GH)

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7
Q

Excess GH is associated with

A

High levels of GH has prolactin-like effects

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8
Q

Ix for Acromegaly

A

IGF-1: high (inital Ix)

OGTT (definitive Ix)

  • Normal: Glucose load –> ↓ GH levels
  • Acromegaly: Glucose load –> Paradoxical ↑ GH levels
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9
Q

Tx for acromegaly

A

(1) Trans-sphenoidal surgery
(2) Somatostatin analogue (Octreotide) or Cabergoline (DA agonist)
(3) GH antagonist
(4) Radiotherapy

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10
Q

Complications of Acromegaly

A

Cardiac complications (40%)

Diabetes mellitus

Colonic adenocarcinoma

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11
Q

Micro vs Macroadeoma

A
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12
Q

Hypothalamic - Pitutiary axes

A
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13
Q

Signs of hypernatraemia

A
  • Thirst
  • Loss of appetite
  • Restlessness
  • ↑ Tone (Spasticity)
  • Hyper-reflexia
  • Tremor
  • Seizures
  • Ataxia
  • Lethargy –> Stupor –> Coma
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14
Q

Signs of hyponataremia

A

If Na+ < 120 mM –> Generalised weakness, Poor mental function, N&V, Irritability

If Na+ < 110 mM –> Confusion, Drowsiness, Seizures, Coma (↓ GCS), Death

SALT LOSS

  • Stupor
  • Anorexia
  • Lethargy
  • Tendon reflexes ↓
  • Limp muscles (weakness)
  • Orthostatic hypotension
  • Seizures
  • Stomach cramps
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15
Q

Signs of hypokalaemia

ECG changes

Tx

A

Sx

  • Muscle weakness
  • Cardiac arrhythmias
  • Polyuria/Polydipsia
  • Constipation

ECG

  • Prolonged PR
  • Flattening of T wave
  • ST depression
  • U wave

Tx

  • Oral/IV Potassium chloride (<10mmol/hr)
  • Treat underlying cause
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16
Q

Sx and ECG changes of hyperkalaemia

A

ECG:

  • Bradycardia
  • Loss of p waves / Flattened p waves
  • Prolonged PR
  • Broad QRS
  • Depressed ST
  • Peaked T waves

Sx of hyperkalaemia MURDER

  • Muscle cramps –> Weakness –> Paralysis
  • Drowsiness
  • Hypotension
  • Arrhthmias
  • Abdominal cramps
  • Diarrhoea
  • Oliguria
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17
Q

Ix for diabetes insipidus

A

Serum osmolality: ↑

Urine osmolality: ↓ (i.e. dilute urine)

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18
Q

Tx for DI

A

Cranial DI –> Desmopressin

Nephrogenic DI –> Thiazide diuretics (Bendroflumethiazide)

==> retain urine volume and bypass VP’s concentrating mechanism

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19
Q

Ix in SIADH

Examination findings

A
  • Plasma osmolality: ↓ plasma osmolality, ↓ Na+
  • Urine osmolality: ↑ urine osmolality, ↑ Urine Na+
  • Euvolaemic

Tx

  • Treat underlying cause
  • Treat hyponataremia
    • Fluid restriction
    • +/- IV Hypertonic 3% saline
      • Avoid increasing Na too quickly (central pontine myelinolysis)
    • +/- Furosemide
  • Long term –> cause nephrogenic DI
    • Lithium
    • DMCT
    • Tolvaptan
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20
Q

Sx of hypopituitarism

A
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21
Q

Tx for thyroid storm

A
  • ABCDE
  • High-dose anti-thyroid drug (Aim to remove excess T4/T3 QUICKLY)
    • Carbimazole
    • Propylthiouracil
  • + Corticosteroids
  • + β-blockers
  • + Iodine (Lugol solution)
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22
Q

Tx for Grave’s disease

A
  • Anti-thyroid drugs (Carbimazole or Propylthiouracil)
    • High dose and titrate or Block and replace
    • Takes time to work due to existing T4/T3 in colloid
    • Given with B-blockers
  • β blockers (Propranolol)
  • Radioactive iodine
  • Surgery
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23
Q

Smooth diffuse goitre

Fever (ALWAYS PRESENT)

Extreme agitation

Confusion / Delirium

Nausea & Vomiting

Tachycardia

Cardiac failure

Liver failure / Jaundice

Signs of dehydration / volume depletion

Diagnosis?

A

Thyroid storm

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24
Q

Thyroid scan in

Grave’s

Plummer’s (toxic nodular goitre)

Toxic adenoma

A

Grave = smooth uptake

Plummer’s (toxic nodular goitre) = hot nodules and cold areas

Toxic adenoma = hot nodule

Viral thyroiditis = no uptake

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25
Q

Thyroid goitre Ix

A

TFTs

Neck USS +/- Fine needle aspiration

Thyroid scan

26
Q

Tx for toxic nodule

A
  • Medical
    • Anti-thyroid drugs (Carbimazole, Propylthiouracil)
    • Beta-blockers
    • Radio-iodine
  • Surgical
    • Subtotal/Total Thyroidectomy
27
Q

Antibody in Hashimoto’s thyroiditis

A

Anti-TPO Ab / Anti-thyroglobulin Ab: +ve

28
Q

Causes of Cushing’s syndrome

A
  • ACTH dependent
    • Pituitary adenoma (Cushing’s disease)
    • Ectopic ACTH production
  • ACTH indepedent
    • Iatrogenic / Exogenous steroids
    • Adrenal adenoma
29
Q

Ix for Cushing’s syndrome

A
  • 24 hour urine cortisol
  • 9am and Midnight cortisol
  • Low dose dexamethasone supression test (Gold standard)
  • High dose dexamethasone supression test

Adrenal adenoma

  • ↓ ACTH
  • ↑ Cortisol

Ectopic ACTH

  • ↑ ACTH
  • ↑ Cortisol – remains high in high-dose suppression test

Cushing’s disease

  • ↑ ACTH
  • ↑ Cortisol on low dose suppression BUT supressed on high-dose suppression test
30
Q

Tx for Cushing’s syndrome

A
  • Conservative
    • If iatrogenic –> ↓ steroid dose
  • Medical
    • Metyrapone (↓ Cortisol synthesis, ↑ aldosterone, ↑ adrenal androgens)
    • Ketoconazole (↓ Cortisol synthesis, ↓ aldosterone, ↓ adrenal androgens)
  • Surgical
    • If Cushing’s disease –> Trans-sphenoidal hypophysectomy
    • If ectopic ACTH –> remove tumour
    • If adrenal adenoma –> adrenalectomy
  • If non-operable –> Radiotherapy
31
Q

Tx of Conn’s syndrome

A
  • Medical
    • MR antagonist
      • Spironolactone
      • Epleronone
    • Anti-hypertensives
  • Surgery
    • Laparoscopic adrenalectomy: remove the tumour

N.B. If bilateral adrenal hyperplasia, stay on spironolactone (do not remove both adrenals as cannot respond to stress)

32
Q

Palpitations

Headache

Episodic sweating (diaphoresis)

Episodic severe hypertension (may cause stroke)

Diagnosis? Ix? Tx?

A

Phaeochromocytoma

24 hour urinary catecholamines (adrenaline, noradrenaline, dopamine) : ↑

Plasma catecholamines levels: ↑

Long term

  • Pre-operative
    • FIRST, α blockade (Phenoxybenzamine)
    • THEN, β blockade (Propanolol)
  • Surgery
    • Laparoscopic adrenalectomy
33
Q

Vomiting

Abdo pain

Tachycardia

Weakness

Pale, Cold, Clammy, Oliguria

Hypoglycaemia

Hypovolaemic shock

+/- Trigger

Diagnosis? Ix? Tx?

A

Addisonian crisis

↓ Na+, ↑ K+

  • High dose IV Hydrocortisone
  • IV 0.9% saline (1L over 30-60min)
    • Aim to restore BP & replace salt that is lost
  • 5% Dextrose (prevent hypoglycaemia)
    *
34
Q

Ix and Tx of Addion’s disease

A

Ix

  • 9am cortisol
    • If normal: HIGH (normally high in the morning)
    • Addison’s: LOW Cortisol (< 100nmol/L is diagnostic)
  • ACTH
    • Addison’s (Primary): HIGH ACTH
  • SynACTHen test + Measure Cortisol (before & after)
    • If normal: ↑ cortisol
    • If Addison’s: no/little increase

Tx for Addisonian crisis

  • High dose IV Hydrocortisone
  • IV 0.9% saline (1L over 30-60min)
  • 5% Dextrose (prevent hypoglycaemia)

Long term Tx

  • Hydrocortisone (replace glucocorticoid)
    • Advice: Increase dosage if (1) acute illness or (2) surgery or (3) stress
  • Fludrocortisone (replace mineralocorticoid)
35
Q

↓ Na+, ↑ K+
Hypotension + Hyperkalaemia

Diagnosis? Causes?

A

Addison’s disease

Autoimmune

TB

Iatrogenic

36
Q

Hypertension

Hypokalaemia

Diagnosis?

A

Hyperaldosteronism

  • Primary
    • Conn’s
    • Bilateral adrenocortical hyperplasia
  • Secondary
    • RAS
    • Renin-secreting tumour
37
Q

Steroid synthesis pathway

38
Q

Complete 21-OH deficiency (most common)

Sx

Ix

Tx

39
Q

Partial 21-OH deficiency

11-OH deficiency

17-OH deficiency

40
Q

Causes of hypercalcaemia

41
Q

Sx and Tx of hypercalcaemia

A

Sx

  • Bones - bone pain +/- fractures
  • Stones - renal calculi
  • Abdo moans - constipation, pancreatitis
  • Psychic groans - confusion, seizures, coma
  • Thrones - polyuria, polydipsia

Tx

  • IV 0.9% saline ++++++++++
  • +/- Bisphosphonates
    • ONLY indication = Hypercalcaemia of Malignancy
    • Otherwise avoid!
  • Treat underlying cause
42
Q

Hypocalcemia - Sx, Causes, Tx

A
  • CATS go numb
    • Convulsions
    • Arrhythmias
    • Tetany
      • Trousseau’s
      • Chvostek’s
    • Paraesthesia
  • Causes
    • ↓ Ca2+ and ↑ PTH
      • Vitamin D deficinecy
      • CKD
      • Pseudohypoparathyroidism (PTH resistance)
    • ↓ Ca2+ and ↓ PTH
      • Surgical (post-thyroidiectomy)
  • Tx
    • Ca - IV Calcium Gluconate
    • Vitamin D
43
Q
  • Bone pain and tenderness
    • Typically lower extremities, lower spine, ribs & pelvis
  • Proximal myopathy / Muscle wasting
  • Waddling gait
  • ↑ risk of fractures
  • Signs of hypocalcaemia
    • Trousseau’s sign
    • Chvostek’s sign

Diagnosis? Ix? Tx?

A

Ostemalacia (Vitamin D deficiency)

↓ Ca2+ , ↓ PO43- , ↑ ALP

Tx: Vitamin D

44
Q

Types of Vitamin D supplementation

A
  • If normal renal function, give precursor (they can convert)
    • Ergocalciferol (25 OH D2)
    • Cholecalciferol (25 OH D3)
  • If renal failure (inadequate 1𝝰 hydroxylation)
    • Alfacalcidol
45
Q

Types of hyperparathyroidism

46
Q

X-ray changes in Primary hyperparathyroidism

A
  • Pepper pot skull (diffuse porotic mottling of skull)
  • Rugger jersey spine (sclerosis of sup / inf vertebral margins w central deminerlisation)
47
Q

Pathology and Signs of pseudohypoparathyroidism

A

PTH resistance

Hypocalcaemia

Abnormal 4th and 5th metacarpal joint

“Knuckle knuckle dimple dimple” sign

48
Q

Osteoporosis - Sx, Ix, Tx

A

Osteoporosis

Asymptomatic until fracture

Ix

  • DEXA score (T score < -2.5 (healthy reference) and Z-score (age-matched control)
  • Normal Ca2+, PO43-, ALP
  • FRAX score / QFRACTURE tool

Tx

  • (1) Bisphosphonates
  • + Ca and Vitamin D supplementation
  • (2) Denosumab (RANKL inhibitor –> inhibitor osteoclasts)
  • (3) Teriparatide (recombinant PTH –> osteoblasts > osteoclasts)
  • Strontium ranelate
  • SERMs
  • HRT
49
Q

Paget’s disease

X-ray changes

Biochemistry

Tx

Cx

A

ALP: ↑↑↑

Ca2+ & PO43-: normal

PTH: normal

Vitamin D: normal

X-ray: Cotton-wool appearance

Tx: Bisphosphonates +/- Analgesia

Cx: Fractures, Osteosarcoma (1%), Sensorineurlal deafness

50
Q

Definitions of diabetes

A
  • Fasting blood glucose: > 7 mmol/L in Diabetes
  • OGTT: > 11.1 mmol/L in Diabetes
  • HbA1c: > 48 mmol/mol is diagnostic for Diabetes (> 6.5%)
    *
51
Q

Tx for T2DM

A

(1) Diet & Exercise
(2) Metformin
(3) See image

52
Q

Complications of T2DM

53
Q

Tx of Hypoglycaemia

54
Q

Altered mental status (Confusion ==> Coma)

Severely dehydration

Hyperglycaemia

↑↑ osmolality

↑ Na+

No ketones

Diagnosis? Tx?

A

Hyperglycaemic Hyperosmolar State

  • IV 0.9% saline
    • Rehydrate with normal saline SLOWLY
    • If corrected too quickly –> cerebral oedema (high mortality)
  • If blood glucose is not falling ==> IV Insulin
  • +/- Anticoagulation
55
Q

Diabetic retinopathy - Stages, Findings, Tx

56
Q

Diabetic nephropathy

Features

Ix

Tx

A

Sx

  • Progressive proteinuria
  • ↑BP

Ix

  • Albumin:Creatinine ratio (ACR)
  • eGFR
  • Proteinuria

Tx

  • ACE inhibitors (aim for BP < 130/80mmHg)
57
Q

Diarrhoea

Flushing

+/- Wheezing

Abdo Pain

Telangiectasia

Diagnosis? Ix? Tx?

A

Carcinoid syndrome

Ix:

  • Serum Chromogranin A/B: ↑
    • Tumour marker
  • 24hr urine collection of 5-hydroxyindoleacetic acid: ↑
    • 5-hydroxyindoleacetic acid is a serotonin metabolite

Tx

  • Acute
    • IV Octreotide +/- IV Hydrocortisone
  • Long-term
    • Surgical resection
58
Q

Tx for Obesity

A
  • Conservative
    • Diet & Exercise
  • Medical
    • Orlistat: lipase inhibitor –> ↓ absorption of dietary fat
    • Lorcaserin: serotonin receptor agonist –> ↓ appetite
    • Liraglutide: GLP-1 receptor agonist –> ↓ appetite
    • Manage comorbidities
  • Surgical
    • Criteria:
      • BMI > 40
      • All other measures ineffective
      • Fit for anaesthesia and surgery
      • Committed to need for long-term follow up
    • Options
      • Roux-en-Y gastric bypass
      • Adjustable gastric banding (Laparoscopic)
      • Sleeve gastrectomy
      • Duodenal switch with biliopancreatic diversion
59
Q

Tx for hypercholesterolaemia / hyperlipidaemia

A

(1) Statins
(2) Ezetimibe
(3) Fibrates (Gemfiibrozil)

60
Q

DDx Goitre

A
  • Iodine deficiency
  • Autoimmune
    • Grave’s disease
    • Hashimoto’s
  • Infection
    • Viral thyroiditis
  • Malignancy
    • Pituitary adenoma
  • Physiological
    • Pregnancy
    • Puberty