Disorders of Adrenal Function Flashcards

1
Q

What is an increased secretion of cortisol called

A

Cushing’s syndrome

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2
Q

What are the causes of Cushing’s syndrome and how do they cause the increased cortisol secretion

A

Adnreal cushing’s - increased adrenal cortex activity due to primary cortisol-producing adrenal adenoma

Cushing’s disease - (bengin) pituitary adenoma causes disorders in secretion of ACTH

Non pituitary-adrenal tumours producing ACTH

External causes - prescribed glucocoricoids to treat chronic inflammatory conditions

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3
Q

What are the signs and symptoms of excess coritsol

A

Increased muscle proteolysis and hepatic gluconeogenesis - hyperglycaemia with polyuria and polydipsia

Increased muscle proteolysis - wasting of proximal muscles (thin arms and legs and muscle weakness)

Increased lipogenesis in adipose - deposition of fat in abdomen, neck and face. Moon-shaped face and weight gain

Purple striae on lower abdomen, upper arms and thighs - catabolic effect on protein structures in skin, easy bruising

Immunosuppressive, anti-inflammatory and anti-allergic reactions cause increased bacterial infection susceptibility

Osteoporosis due to disturbance in Ca metabolism and loss of bone matrix protein

Hypertension due to Na and fluid retention

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4
Q

What is a disease of decreased cortisol secretion called

A

Addison’s disease

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5
Q

How might Addison’s disease be caused

A

Diseases of adrenal cortex - i.e. auto-immune destruction

Disorders in pituitary or hypothalamus - decreased ACTH or CRF production

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6
Q

What is Addison’s crisis and how may it present

A

Life-threatening disease due to adrenal insufficiency

Symptoms:

Nausea, vomiting, extreme dehydration, hypotension, confusion, fever, coma

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7
Q

What are the symptoms of Addison’s disease

A

Initially non-specific: tiredness, extreme muscular weakness, anorexia, vague abdominal pain, weight loss, occasional dizziness

Extreme muscular weakness and dehydration

Increased skin pigmentation - especially exposed areas, points of friction, buccal mucosa, scars and palmar creases

Decreased BP - Na and fluid depletion

Postural hypotension - fluid depletion

Hypoglycaemic episodes

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8
Q

What clinical tests can be used for adrenocortical function

A

Measurement of plasma cortisol and ACTH levels

24hr urinaru excretion of cortisol and its breakdown products

Dexamethasone suppression test - dexamethasone suppresses ACTH secretion as it is a potent synthetic steroid

ACTH simtulation test - synacthan normally increases plasma cortisol

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9
Q

What is congenital adrenal hyperplasia

A

There is a gentic defect in one or more of the enzymes required for synthesis of corticosteroid hormones from cholesterol, meaning cortisol is not produced

Due to lack of cortisol, pituitary is not inhibited by negative feedback so secretes large amounts of ACTH, causing adrenal cortex hyperplasia

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10
Q

What is the most common form of congenital adrenal hyperplasia and what effect can it have

A

Defect in 21-hydroxylase

Results in less glucocorticoid and mineralocorticoid production

This causes precursor of these hormones to be used in androgen synthesis

This can result in genital ambiguity in female infants and a high rate of Na loss in urine - salt-wasting crisis

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11
Q

What is primary hyperaldosteronism called and what can it be caused by

A

Conn’s syndrome

Hyperactivity of one or both adrenal glands

Unilateral - adenoma

Bilateral - genetic syndromes

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12
Q

What are the signs and symptoms of Conn’s syndrome

A

High BP

Occasional muscular weakness and spasms

Tingling sensations

Excessive urination

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13
Q

What do androgens stimulate in males

A

Growth and development of male genital tract

Height

Body shape

Facial and body hair

Lower voice pitch

Anabolic actions - especially on muscle protein

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14
Q

What effects does over secretion of adrenal androgens have in females

A

Hirsutism - excessive body hair growth

Acne

Menstrual problems

Virilisation

Increased muscle bulk

Deepening voice

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15
Q

What do oestrogens stimulate in females

A

Growth and development of female genital tract and breasts

Broad hips development

Accumulation of fat in breasts and buttocks

Body hair distribution

They are weakly anabolic and decrease circulating cholesterol levels

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16
Q

What are the two forms of hyperaldosteronism and how can they be classified

A

Primary - defect in adrenal cortex, characterised by lower renin levels

Secondary - over active RAAS, characterised by high renin levels

17
Q

What are the signs of hyperaldosteronism

A

High BP

LV hypertrophy

Stroke

Hypernatraemia

Hypokalaemia

18
Q

What is a chromaffin cell tumour called and what does it secrete

A

Phaeochromocytoma

Secretes excess catecholamines like adrenaline and noradrenaline

19
Q

What are the symptoms of phaeochromocytoma

A

Hypertension

Anxiety

Palpitations

Pallor

Diaphoresis - excessive sweating

Glucose intolerance - and elevated blood glucose

Weight loss

Headaches