Endocrinology Flashcards

1
Q

Types of thyroid cancer?

A
  • Papillary
  • Follicular
  • Medullary associated with raised calcitonin (an antagonist to PTH)
  • Anaplastic
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2
Q

 Management of thyroid cancer?

A
  • Hemi-thyroidectomy (± total) + Iodine-131 given to kill all remaining thyroid cells
  • Follow-up (yearly) – if +ve, then administer more I-131:
    o I-123 whole body scans
    o Thyroglobulin (TG) measurements / calcitonin (if medullary)
  • Remission for 7 years  fully cured and can be discharged
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3
Q

Causes of hyperthyroidism?

A

High-uptake
Grave’s disease (anti-TSH antibodies)
Toxic multinodular goitre
Single toxic adenoma

Low-uptake
Postpartum thyroiditis
Sub-acute thyroiditis
Viral thyroiditis
de Quervain’s thyroiditis

 Rare causes:
* Silent thyroiditis (AI, amiodarone) Factitious thyroiditis
* TSH-induced Thyroid cancer induced
* Trophoblastic tumour (high hCG production)

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4
Q

Features of grave’s disease

A
  • Diffuse goitre
  • Thyroid Eye Disease (due to TSH-r on eye muscles)
    o Radioiodine  Graves’ eye disease worse
  • Thyroid-associated dermopathy (pretibial myxoedema)
  • Thyroid acropachy
  • Hx or FHx or autoimmune disease
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5
Q

Best preventative measure of grave’s disease?

A

Smoking cessation

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6
Q

S/S of thyroid storm (can be precipitated by radioiodine)?

A

S/S: hyperthermia, tachycardia, jaundice, altered mental status, cardiac (AF, high-output HF)

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7
Q

Mx of thryoid storm?

A

IV propranolol - thionamides (PTU), hydrocortisone - iodine (~1-4 hours after ATDs)

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8
Q

Graves’ disease mx:

A
  • 1st (given in primary care): propranolol (not bisoprolol)
  • 1st line, likely remission with ATDs: ATDs
     1st line: Carbimazole, 40mg (then reduce)
     2nd line: PTU (pregnancy, <6m attempt for conception, pancreatitis)
    o Method:
     [1] Titration (12-18m; dose on TFTs – once euthyroid, gradually reduce)
     [2] Block and replace (6-9m; fixed high dose carbimazole, incl. thyroxine)
  • 1st line, unlikely remission with ATDs: Radioiodine (I-131):
    o CI: pregnancy, <16yo, thyroid eye disease
    o SE: hypothyroidism, thyroid storm
  • Surgery (in the run up to surgery… needs to be euthyroid)
    o (1) thionamides (stop 10 days pre-surgery as increases vascularity); OR propranolol
    o (2) laryngoscopy (check vocal cords)
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9
Q

Causes of hypothyroidism:

A
  • Hashimoto’s (most common UK; associations: IDDM, pernicious anaemia, Addison’s disease)
    o Ix: anti-TPO ABs
  • Reidel’s thyroiditis
  • Sub-acute thyroiditis / viral thyroiditis / de Quervain’s thyroiditis (hypothyroid phase)
  • Iatrogenic:
    o Post-Graves’ disease (radioactive iodine, surgery, natural history or thionamines)
    o Drugs (amiodarone, lithium)
  • Iodine deficiency (most common in the developing world)
  • Sub-clinical (subclinical) hypothyroidism:
    o S/S: none
    o Ix: TSH elevated, T4 normal
    o Mx (if TSH >10; otherwise watchful waiting): levothyroxine
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10
Q

Mx of hypothyroidism?

A
  • Start 50-100 mcg, OD [25mcg in elderly or IHD*]  check TFTs in 8-12 weeks
  • Aim for a normal TSH (0.5-2.5mU/L)
  • Hypothyroid women in pregnancy  increase T4 by 25-50mcg
  • Interactions (give T4 at least 4 hours before / 4 hours after interacting medications):
    o Iron
    o CaCO3
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11
Q

Symptoms and management of myxoedema coma?

A

 S/S: hypothermia, hyporeflexia, bradycardia, seizures
 Mx: IV thyroxine, IV hydrocortisone, IV fluids

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12
Q

Ix for addison’s disease?

A

o 1st: (9am) plasma cortisol (can be done at any time if doing a full short SynACTHen test):
 >500nmol/L = unlikely Addison’s (>276nmol/L = normal)
 <500nmol/L = short SynACTHen test (still done if suspicion as could be partial insufficiency)
o 2nd: administer SynACTHen 250ug IM
o 3rd: plasma cortisol at 30 minutes (<497nmol/L = Addison’s)

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13
Q

Causes of addisonian crisis?

A

autoimmune (UK), TB (worldwide)
 Sepsis or surgery causing an acute exacerbation of chronic insufficiency (Addison’s, Hypopituitarism)
 Adrenal haemorrhage (Waterhouse-Friderichson syndrome from meningococcaemia)
 Steroid withdrawal

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14
Q

Mx of addisonian crisis:

A

 Initial management:
* 1st  IM hydrocortisone (100mg, STAT)
* 2nd  IV fluid bolus (0.9% saline, >90 SBP) ± glucose
 Continuing management:
* IV fluids
* IV/IM hydrocortisone (100mg/8h)  convert to PO dexamethasone after 72 hours

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15
Q

How is hydrocortisone delivered in an addisonian crisis?

A

IM

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16
Q
  • Signs & symptoms of pituitary adenoma?
A

o Excess hormones (e.g. Cushing’s disease acromegaly, amenorrhea & galactorrhoea)
 Men (prolactinoma)  impotence, decreased libido, galactorrhoea
 Women (prolactinoma)  infertility, decreased libido, galactorrhoea, amenorrhoea, osteoporosis
o Depletion of a hormone(s) (due to compression of the normal functioning pituitary gland)  hypopituitarism
o Headaches (stretching of the dura within/around pituitary fossa)
o Bitemporal hemianopia

17
Q

First line Ix for acromegaly?

A

serum IGF-1
2nd line is OGTT
3rdl line is MRI brain with contrast

18
Q

Mx for acromegaly?

A

 1st line (surgical) - transsphenoidal transnasal hypophysectomy
 2nd line:
* Somatostatin analogue (octreotide) > dopamine agonists (bromocriptine, cabergoline)
* Pegvisomant (GH-R antagonist)

19
Q

Mx for prolactinoma?

A

Medical mx is FIRST LINE, surgical mx is SECOND LINE
 1st line (medical)  bromocriptine, cabergoline
 2nd line (surgical)  transsphenoidal transnasal hypophysectomy

20
Q
A