Adrenal Gland Flashcards
11-Beta Hydroxylase
Synthesis Action and Deficiency Presentation/Lab Values
Makes corticosterone and cortisol
Presents with Hypertension, virulization and ambiguous genitalia
Low aldosterone, cortisol, potassium and renin
High androgens
21-Alpha Hydroxylase
Synthesis Action and Deficiency Presentation/Lab Values
Oxidizes progesterone for aldosterone and cortisol
Presents with hypotension, salt wasting and pernicious puberty
Low aldosterone, cortisol, sodium
High androgens, potassium and renin
17-Alpha Hydroxylase
Synthesis Action and Deficiency Presentation/Lab Values
Makes 17-OH Pregnenolone
Presents with HTN and lack of sexual development
Low cortisol, androgens and potassium
High aldosterone
Cortisol Secretion Stimulation
Stimulated by ACTH from AP
Stimulated by stress and circadian rhythm (increased in AM)
Cortisol Secretion Negative Feedback
Cortisol feeds back on hypothalamus and anterior pituitary
Decreases CRH and ACTH
Exogenous glucocorticoids feed back on same loop
Aldosterone Stimuli
Increased angiotensin, potassium, ACTH and stress
or
Decreased sodium, blood pressure
Cushing’s Syndrome (primary adrenal excess)
Pathophysiology, Presentation and Diagnosis
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
Cushing’s Disease (secondary adrenal excess)
Pathophysiology and Diagnosis
Anterior Pituitary adenoma
Causes increased ACTH/Cortisol and decreased CRH
Diagnosed with positive high dose Dexamethasone test
Decreased ACTH after dose
Hyperpigmentation
Cause and Associated Diseases
Increased ACTH
Seen in Cushing’s Disease and Addison’s Disease
Ectopic ACTH Tumor
Pathophysiology and Diagnosis
Form of Cushing’s Syndrome
Adrenal ACTH adenoma
Increased Cortisol and decreased CRH/plasma ACTH
Diagnosed with negative dexamethasone test
Latrogenic Hypocortisolism
Pathophysiology
Form of Cushing’s Syndrome
Excessive exogenous glucocorticoids
Causes decreased CRH/ACTH/Endogenous Cortisol
Addison’s Disease (primary adrenal insufficiency)
Pathophysiology, Presentation, Lab Values and Diagnosis
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
Secondary/Tertiary Adrenal Insufficiency
Pathophysiology, Lab Values, Diagnosis
Caused by decreased ACTH from Pituitary Gland
Decreased ACTH/Cortisol
Normal Salt Balance/Aldosterone (RAAS)
Diagnose with increased cortisol after cosyntropin
Hyperaldosteronism Cause
Primary and Secondary
Primary: Zona glomerulosa adenoma causing increased aldosterone and decreased renin
Secondary: Excessive renin secretion or 17-Alpha Hydroxylase defect
Hypoaldosteronism Cause
Adrenal gland destruction or aldosterone synthesis issue
11-Beta or 21-Alpha Hydroxylase defects