Adrenal Gland Flashcards

1
Q

11-Beta Hydroxylase

Synthesis Action and Deficiency Presentation/Lab Values

A

Makes corticosterone and cortisol

Presents with Hypertension, virulization and ambiguous genitalia

Low aldosterone, cortisol, potassium and renin
High androgens

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2
Q

21-Alpha Hydroxylase

Synthesis Action and Deficiency Presentation/Lab Values

A

Oxidizes progesterone for aldosterone and cortisol

Presents with hypotension, salt wasting and pernicious puberty

Low aldosterone, cortisol, sodium
High androgens, potassium and renin

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3
Q

17-Alpha Hydroxylase

Synthesis Action and Deficiency Presentation/Lab Values

A

Makes 17-OH Pregnenolone

Presents with HTN and lack of sexual development

Low cortisol, androgens and potassium
High aldosterone

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4
Q

Cortisol Secretion Stimulation

A

Stimulated by ACTH from AP

Stimulated by stress and circadian rhythm (increased in AM)

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5
Q

Cortisol Secretion Negative Feedback

A

Cortisol feeds back on hypothalamus and anterior pituitary
Decreases CRH and ACTH

Exogenous glucocorticoids feed back on same loop

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6
Q

Aldosterone Stimuli

A

Increased angiotensin, potassium, ACTH and stress
or
Decreased sodium, blood pressure

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7
Q

Cushing’s Syndrome (primary adrenal excess)

Pathophysiology, Presentation and Diagnosis

A

Zona fasciculata adenoma
Causes decreased CRH/ACTH and increased cortisol

Presents with trunk obesity, moon face, buffalo hump, easy bruising, immunodeficiency

Diagnosed with negative Dexamethasone test

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8
Q

Cushing’s Disease (secondary adrenal excess)

Pathophysiology and Diagnosis

A

Anterior Pituitary adenoma
Causes increased ACTH/Cortisol and decreased CRH

Diagnosed with positive high dose Dexamethasone test
Decreased ACTH after dose

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9
Q

Hyperpigmentation

Cause and Associated Diseases

A

Increased ACTH

Seen in Cushing’s Disease and Addison’s Disease

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10
Q

Ectopic ACTH Tumor

Pathophysiology and Diagnosis

A

Form of Cushing’s Syndrome
Adrenal ACTH adenoma
Increased Cortisol and decreased CRH/plasma ACTH

Diagnosed with negative dexamethasone test

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11
Q

Latrogenic Hypocortisolism

Pathophysiology

A

Form of Cushing’s Syndrome
Excessive exogenous glucocorticoids
Causes decreased CRH/ACTH/Endogenous Cortisol

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12
Q

Addison’s Disease (primary adrenal insufficiency)

Pathophysiology, Presentation, Lab Values and Diagnosis

A

Autoimmune adrenal destruction of adrenal hemorrhage
Causes decreased mineral/glucocorticoids

Presents with hyperpigmentation and hypoglycemia

Increased CRH/ACTH/Potassium
Decreased Cortisol/Aldosterone/Sodium/Glucose

Diagnose with no effect on cortisol aftercosyntropin

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13
Q

Secondary/Tertiary Adrenal Insufficiency

Pathophysiology, Lab Values, Diagnosis

A

Caused by decreased ACTH from Pituitary Gland

Decreased ACTH/Cortisol
Normal Salt Balance/Aldosterone (RAAS)

Diagnose with increased cortisol after cosyntropin

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14
Q

Hyperaldosteronism Cause

Primary and Secondary

A

Primary: Zona glomerulosa adenoma causing increased aldosterone and decreased renin

Secondary: Excessive renin secretion or 17-Alpha Hydroxylase defect

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15
Q

Hypoaldosteronism Cause

A

Adrenal gland destruction or aldosterone synthesis issue

11-Beta or 21-Alpha Hydroxylase defects

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16
Q

Pheochromocytoma

Pathophysiology, Presentation, Lab Values

A

Adrenal medulla adenoma causing excessive catecholamine secretion

Presents with extreme HTN, sweating, increased HR, pale

Shows increased metanephrine/normetanephrine

17
Q

Catecholamine Synthesis Steps

A

ACTH increases DOPA which becomes Dopamine
Ach causes DA to become Norepinephrine
Cortisol causes NE to become Epinephrine using PNMT enzyme

18
Q

Catecholamine Degradation

Enzyme, Products, Excretion

A

Uses catecholamine-O-methyltransferase (COMT)

Epinephrine made into metanephrine
Norepinephrine made into normetanephrine

Excreted as Vanillylmandelic acid (VMA)