Investigating the Endocrine System Flashcards

1
Q

Types of hormone

A

Peptide (e.g PTH, ACTH, TSH)
Steroid (e.g. Testosterone, Oestradiol, Cortisol)
Tyrosine-based (e.g. T3, T4)

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2
Q

TBG

A

Carries thyroid hormone but only unbound forms are physiologically active
If level of TBG changes, this results in a change in the level of the free hormones
Therefore measurement of total hormone levels can be misleading

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3
Q

Causes of increased TBG

A

Genetics
Pregnancy
Oestrogens

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4
Q

Causes of decreased TBG

A
Genetics
Protein-losing status
Malnutrition
Malabsorption
Acromegaly
Cushing's
High dose corticosteroids
Severe illness
Androgens
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5
Q

Low TSH, low thyroxine

A

Pituitary failure

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6
Q

Low TSH, high thyroxine

A

Thyroid gland overproduction (e.g. Graves’)

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7
Q

High TSH, low thyroxine

A

Unresponsive thyroid

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8
Q

High TSH, high thyroxine

A

Pituitary gland overproduction or feedback fails (rare)

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9
Q

“Sick euthyroid disease”

A

No point in measuring thyroid hormones in critically unwell patients - will be all over the place and difficult to interpret

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10
Q

Repetition of TFTs (guidelines)

A

Repeat every 3 years in healthy patients (unlikely)
Graves’ - 1-2 months after radioactive iodine, then 4-6 week intervals if remain thyrotoxic, or 6-8 weeks following thyroidectomy
Hypothyroidism - 2 months, but not before this due to lag period of thyroxine, if stabilised, then annually

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11
Q

Immunoassays

A

Use of monoclonal antibodies
Alternative labelling for H&S reasons
Widely used due to antibody specificity, sensitivity and that it is amenable to automation

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12
Q

Interference in immunoassay

A

Cross-linking antibody causing positive interference
Blocking antibody causing negative intereference
Usually a different test done if the test results do not match the patient

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13
Q

Clinical features of phaeochromocytomas

A
Excessive and episodic release of catecholamines may results in paroxysmal features:
Hypertension
Sweating, pallow
Panic attacks
Headaches
Abdo pain
Can also be asymptomatic
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14
Q

Testing for phaeochromocytomas

A

Using epinephrines due to the fact that it is more stable in the blood than catecholamines

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15
Q

Whipple’s Triad

A

Signs and symptoms of hypoglycaemia
Low plasma glucose
Resolution of symptoms once glucose level rises

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16
Q

Symptoms of hypoglycaemia

A

Hunger, sweating, anxiety parenthesis, palpitations, tremulousness, weakness, fatigue, dizziness, headache, confusion, behavioural changes, cognitive dysfunction, blurred vision, diplopia

17
Q

Signs of hypoglycaemia

A

Pallor, tachycardia, widened pulse pressure, cortical blindness, hypothermia, seizures, coma

18
Q

Common endogenous causes of hypoglycaemia

A
Insulinomas
Insulin antibodies
Critical organ failure
Sepsis
Hormone deficiency
19
Q

Common exogenous causes of hypoglycaemia

A

Overuse of insulin
Drug interactions
Alcohol or other toxins

20
Q

Insulinoma

A

Most common tumours from islets of Langerhans
Highest incidence 40-60 years
More females than males

21
Q

Diagnosis of insulinoma

A

Fasting blood test
Low blood sugar (less than 2.2 mol/l)
High insulin (6 microunits/ml or higher)
High levels of C peptide (0.2 mol/l or higher)

22
Q

Features of Cushing’s syndrome

A
Obesity - moon face, central obesity, shoulders
Skin - thin, purple striae, bruising
Hypertension
Glucose intolerance
Menstural disturbances/impotence
Thin limbs/muscle weakness
Back pain from osteoporosis
Psychiatric disturbances - depression, psychoses
23
Q

Difference between Cushing’s syndrome and disease

A

Cushing’s syndrome is any high cortisol condition

Cushing’s disease is specifically pituitary ACTH secreting tumour

24
Q

Causes of Cushing’s syndrome

A

Pituitary ACTH secreting tumour (Cushing’s disease)
Cortisol producing tumour in the adrenal gland
Ectopic ACTH producing tumour
Iatrogenic

25
Q

Dexamethasone test

A

Test for Cushing’s
High cortisol should be decreased in an overnight suppression test with dexmethasone 1mg
If cortisol does not decrease - Cushing’s can be diagnosed