ENDO1 Flashcards

(55 cards)

1
Q

Phaeo symptoms

A

Palps Anxiety Sweating Headache Tremor Hypertension Nausea

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2
Q

Phaeo Cause

A

Catecholamine producing tumour in adrenal medulla

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3
Q

Phaeo Ix

A

Free plasma metanephrines. 24 urinary catecholamines and metanephrines

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4
Q

Phaeo Mx

A

Surgery - remove tumor Whilst they wait - add phenoxybenzamine 10mg bd till get to target BP of 120/80 Alphablockade often causes reflex tachy So ONCE evidence of 1) symptoms stopped 2) target BP reached 3) Postural drop is 20/10 then can start metoprolol 50mg bd

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5
Q

Cushings sx

A

Thin skin Facial puffiness/swelling Peripheral Oedema Hypertension Diabetes Buffalo hump Hirsutism (With androgens) Proximal myopathy Central obesity with striae Depression Psychosis Osteoporosis with pathological fracture Avascular necrosis of head of femur amenorrhea loss of libido

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6
Q

Cushings Initial investigations?

A

Overnight 1mg dexamethasone test PLUS one of: Free 24 hr urinary cortisol (two measurements) Free late night salivary cortisol (two measurements) When 2 of these tests are abnormal - diagnosis. If only one positive -needs further evaluation to exclude physiologic hypercortisolism and confirm diagnosis - REFER TO ENDO

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7
Q

What are the Sx of hyperthyroidism?

A

weightloss, tremors, flushing, heat intolerance, anxiety, increased frequency of defecation, increased appetite, psychosis, palpitations NB: A patient may just present with anxiety

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8
Q

What are the examination findings of hyperthyroidism?

A

Tachycardia, Postural tremor , warm/sweaty peripheries, may have atrial fibrilliation, proximal muscle weakness, hyperactive reflexes, thyroid enlargement or irregularity, Pempertons sign (thoracic inlet obstruction) (IN GRAVES - thyroid acropachy, pretibial myxoedema, opthalmopathy - exopthalmos, proptosis, lid lag, lid retraction, keratitis/chemosis, opthalmoplegia) NB: elderly pt may present only with HF or AF

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9
Q

Suppressed TSH with Normal T3/T4

A

Subclinical hyperthyroid

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10
Q

Suppressed TSH with elevated T3/T4

A

overt hyperthyroidism

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11
Q

Elevated TSH, with elevated T3/T4

A

TSH producing pituitary adenoma - check TRH

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12
Q

Uptake will be increased on radioactive iodine scan

A

TMNG, TA, Graves

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13
Q

Uptake will be decreased on radioactive iodine scan

A

Thyroiditis

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14
Q

A person with diabetes who presents unconscious, drowsy or unable to swallow AND Hypoglycaemia - Mx?

A

Management is as follows: • Commence appropriate resuscitation protocols. • Give an injection of glucagon 1 mg intramuscular or subcutaneous if available. • If intravenous access is obtained, glucose 50% – 20 mL intravenous via a securely positioned cannula (optimally the antecubital veins). Use 10% glucose in children, as hyperosmolality has caused harm. • Phone for an ambulance (dial 000) stating a ‘diabetic emergency’. • Wait with the patient until the ambulance arrives. • When the person regains full consciousness and can swallow, they can then be orally given a source of carbohydrate.

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15
Q

Contraindications for radioactive iodine?

A

Pregnancy, breastfeeding, or planning pregnancy within 6 months of treatment

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16
Q

Sideeffects of antithyroid drugs? Minor and major?

A

Minor: Pruritis Urticaria Gastrointestinal upset arthralgia fever altered taste Major: AGRANULOCYTOSIS (check FBE - leukopenia) thrombocytopenia aplastic anaemia cholestatic jaundice (carbimazole) hepatitis (propylthiouracil)

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17
Q

Compare and contrast the treatments for Graves disease?

A
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18
Q

Firstline treatement for Graves?

A

Antithyroid meds

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19
Q

Firstline treatment for TMNG?

A

RAI unless contraindicated

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20
Q

Firstline treatment for TA?

A

RAI unless contraindicated

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21
Q

How does postpartum thyroiditis clinically present?

A
  • Typically 1-6 months after delivery
  • Common in women with T1DM
  • Diffuse, small goitre
  • Hyperthyroid for 1-2 months followed by hypothyroid for 4-6months
  • Hypothyroidism may be permanent (20%)
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22
Q

Treatment of postpartum thyroiditis?

A

Betablocker for hyperthyroid symptoms

THyroxine if hypothyroid phase is prolonged and/or symptomatic, breastfeeding or trying to conceive

TPO Ab will have high titre because autoimmune basis

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23
Q

Cause of subacute thyroiditis?

Clinical features?

A

Post viral syndrome, destruction of thyroid follicles with released of stored thyroid hormone

Features:

Female to Male 5:1

Peak age of onset 20-60

TENDER goitre

Often following acute URTI

Hyperthyroid for 1-2 months followed by hypothyroid for 4-6 months (hypo may be permanent in 10%)

24
Q

Tests to order in hyperthyroidism?

A

TSH initially - repeat in 4 weeks if asymptomatic or immediately if symptoms

T3 and T4

TSH recepter antibodies (specific for Graves)

Thyroid antibodies - antithryoglobulin, antimicrosomal, antithyroperoxidase (anti TPO - best if there is an autoimmune cause eg thyroiditis, can also be positive in graves)

ESR will be elevated in subacute granulomatous thyroiditis

TRH only check if tsh, t3 and t4 are elevated - looking for TSHoma

Imaging: U/S and radioisotope scan

25
When does a radionuclide scan not need to be ordered in hyperthyroidism?
diffusely swollen goitre, recent onset of opthalmopathy, moderate to severe thyrotoxicosis - presumptive dx of graves -
26
Management of Graves disease?
1. Establish diagnosis and confirm complicatins (cardiac and osteoporosis) 2. Treat Tachycardia with BB if symptomatic: PROPRANOLOL 10mg BD Orally initially, increase to 40mg BD according to Heart rate 3. Antithyroid medications USUALLY Carbimazole (less sideeffects) than PTU Initial dose: 10 to 20mg orally daily - can increase up to 45mg in 2-3 divided doses IF PREGNANT T1: PTU (carbimazole- embryotoxicity) then convert to carbimazole in T2 and T3 (as PTU can cause a hepatitis) PTU dose: 200mg orally daily (can increase up to 600mg a day in 2 -3 divided doses). 4. Educated patient about important major sideeffects - Attend clinic if any fever, infection, mouth ulcers, sore throat, for Full blood examination (both CBZ and PTU can cause agranulocytosis) Attend if severe itchiness, fatigue, nausea, abdo pain, pale stools, jaundice, - PTU can cause a hepatitis/CBZ can cause hepatocellular jaundice)
27
What is the acute management of agranulocytosis?
Urgent transfer to Emergency deparment for admission Intravenous antibiotics Intravenous G-CSF (granulocyte colony stimulating factors)
28
How would you treat subacute thyroiditis?
1. Betablocker for tachycardia - Propranolol 10mg bd orally intially increasing up to 40mg three times a day if needed. 2. Non steroidal anti inflammatory for pain: Ibuprofen 400mg three times a day orally 3. For prolonged syptoms - Prednisolone 40mg orally once daily. Wean over 2 - 4 week period.
29
What is an adrenal incidentaloma
An adrenal lesion (greater than or equal to 1cm) that is found incidentally on imaging for other purposes.
30
Which initial screening tests/biochemical evaluation do you perform an adrenal incidentaloma?
**1. 1mg overnight dexamethasone suppression test.** **2. 24 hr urinary metanephrines and catecholamines** **IF HYPERTENSIVE:** **3. Plasma aldosterone: Plasma Renin activity Ratio** IF ANY of the above are **positive**: then if symptomatic - refer to surgeon for adrenalectomy. If asymptomatic - Refer patients under the age of 40. Over the age of 40 and Unfit for surgery - surveillance IF the tests are negative - and either greater than or equal to 4cm OR suspicious imagin findings - refer to surgeon for adrenalectomy (cos maybe malignant) If negative and less than 4cm in size and benign looking on Imaging - Surveillance - Yearly Biochem eval for five years; Repeat CT in 6 months then yearly for two years.
31
Infant presents with failure to thrive, salt losing enteropathy and virilisation/ambiguous genitalia. What is the most likely cause?
Congenital adrenal hyperplasia
32
What is the genetic inheritance pattern and pathophysiology of congenital adrenal hyperplasia?
Autosomal recessive. (Therefore more common in consanguinous relationships, may have Fam hx of neonatal death). Usually Lacking 21-hydroxylase which helps turn adrenal precusor molecules to 1) cortisol and 2) aldosterone. This means that when ACTH stimulates the adrenal all those precursor molecules turn into androgens. Presents with virilisation, failure to thrive +/- salt losing crisis(diarrhoea/vomiting) (hyponatraemia and hyperkalaemia)
33
How does Congenital adrenal hyperplasia usually present?
1. In early infancy - with virilisation of female genitalia. 2. Failure to thrive. 3. Diarrheoa and vomiting as part of salt losing crisis. (Endocrine emergency).
34
How do you manage Congenital adrenal hyperplasia?
1. Lifelong glucocorticoid and mineralocorticoid replacement. (hydrocortisone and fludrocortisone) 2. Screen all first degree relatives for CAH.
35
What are the causes of Addissons disease?
Most common in West – Autoimmune adrenalitis Worldwide – TB, fungal infections (Cryptococcus/histoplasmosis), CMV Acute haemorrhage (eg meningococcal septicaemia)
36
What is the underlying pathology in Addisons disease?
Destruction of adrenal cortex.
37
What are the types of adrenal insufficiency?
Primary – a) autoimmune adrenalitis b) congenital adrenal hyperplasia c) adenoma d) idiopathic Secondary – Reduced ACTH from hypopitutarism
38
What are the signs and symptoms of Addisons disease?
Symptoms of cortisol deficiency: weakness, fatigue, anorexia, weight loss, diarrheoa and vomiting, hypoglycaemia, Symptoms of aldosterone deficiency: Hyponatraemia, Hyperkalaemia, acidosis, tachycardia, hypotension, salt cravings Symptoms of ACTH increase( in primary adrenal insuff): Generalised hyperpigmentation (look especially in non sun exposed areas eg palmar creases and axilla)
39
When should an acute adrenal crisis be considered?
Any one of the following: altered conscious state, circulatory collapse, hyponatraemia, hypoglycaemia, hyperkalaemia,
40
Investigations in acute adrenal insufficiency?
Serum glucose, urea, sodium, potassium, blood gas analysis
41
Management of Acute adrenal insufficiency
Urgent transfer to hospital for emergency management IV therapy If severe dehydrated – 20ml/kg 0.9 NACL Intravenous bolus If moderate dehydration – 10ml/kg 0.9 NACL IV Maintenance – 5% dextrose Steroid replacement with IV hydrocortisone (100mg initially) Correct hypoglycaemia Correct hyperkalaemia (with fluids initially) if K+ is greater than 6 – ECG and cardiac monitoring
42
What advice would you give to someone with addisons disease to prevent an acute adrenal crisis?
Emergency Action plan Emergency identification – Medic Alert bracelet Triple normal oral Glucocorticoid maintenance dose for 2-3 days during stress (fever/fracture) Administer IM hydrocortisone if oral medication not tolerated (vomiting) Consider Increase parenteral dose of hydrocortisone before anaesthesia and post operatively Ensure patients have ambulance cover and ready to use IM hydrocortisone vial (Act-O-Vial) for emergencies
43
What is the definitive test for Addisons disease?
Short synathcen test
44
What hormones are secreted by the anterior pituitary gland?
Adrenocorticotophic hormone (ACTH) Thyroid stimulating hormone (TSH) Growth hormone (GH) Prolactin Follicle stimulating hormone (FSH) Luteinising hormone (LH)
45
What hormones are secreted by the posterior pituitary?
Arginine vasopressin (Antidiuretic hormone) Oxytocin
46
What are the symptoms of hypopituitarism in adults?
Amenorrhea Sexual dysfunction Fatigue Depression Altered mental state Cold intolerance Postural light headedness
47
What are the physical signs of hypopituitarism in adults?
Marked pallor Loss or lack of body heair Fine wrinkling of the face Delay in return of reflexes Testicular atrophy Orthostatic hypotension
48
What are symptoms and signs of hypopituitarism in children?
Hypoglycaemia – due to combined ACTH and GH def Prolonged neonatal jaundice (giant cell hepatitis) Micropenis Undescended testes in infancy Growth failure Delayed puberty
49
What biochemical findings suggestive of hypopituitarism?
Low T4 in the absence of high TSH Adults – low estrogen and androgens without elevated LH or FSH
50
What causes hypopituitarism in adults?
Commonly pituitary adenoma Others- prior cranial radiotherapy, head injury, SAH, post partum haemorrhage
51
Causes of hypopituitarism in children?
Genetic Post surgery or radiotherapy
52
Causes of myocarditis?
=
53
Advantages and Disadvantages of Anti thyroid meds in Graves
**Advantages:** 1. *non invasive* 2. *no exac of opthalmopathy* 3. *cheap* 4. *outpatient therapy* 5. *low risk of hypthyroid* **Disadvantages** 1. *Low rate of long term remission* 2. *Adverse drug effects* 3. *Compliance* 4. *Monitoring*
54
Advantages and disadvantages of radioactive iodine for treatment of graves?
**Advantages** 1. Most *_cost effective_* (not cheapest) 2. Few advers effects 3. Outpatient therapy 4. Reduction in goitre size **Disadvantages** 1. Can lead to permanent hypothyroid 2. Development or exacerbation of ophthalmopathy in 15% 3. Need to delay preg and avoid b/feeding 4. Radiation safety precautions 5. Radiation thyroiditis in 10%
55
Advantages and disadvantages of thyroidectomy for graves
**Advantages** 1. Rapid and effective 2. Likely no exacerbation of opthalmopathy, but requires further study **Disadvantages** 1. Permanent hypothyroidism 2. Surgical complications (recurrent laryngeal nervedamage, hypoparathyroid) 3. Most expensive option 4. Scarring 5. Post operative pain or discomfort