Endocrine Flashcards
Pituitary hormones: anterior
Somatotrophs –> HGH
Thyrotrophs –> TSH
Gonadotrophs –> FSH/LH
Lactotrophs –> prolactin
Corticotrophs –> ACTH and MSH
Pituitary hormones: posterior
NOT produced in posterior pituitary; merely stored and secreted there
Oxytocin
ADH
Pituitary gigantism
GH hypersecretion before epiphyseal plates close
Increased stature but little bony deformity.
Hypersomatotropism
Excessive GH secretion
Gigantism
Acromegaly
Acromegaly
Excessive GH in adulthood
Distinctive coarsening features, joint degeneration, peripheral neuropathies
Increased risk of cardiac disease, GI cancer, hypertension
Prolactinoma
Benign tumour of the pituitary gland causing excess prolactin secretion
Symptoms caused by excess circulating prolactin or by pressure of tumour on surrounding tissues
Idiopathic. May be stress related
40% pituitary tumours produce prolactin
Prolactinoma: Sx
Hyperprolactaemia
Pain, visual disturbances from macroprolactinoma
Amenorrhea (hyperprolactinaemia disrupts gonadotropin secretion –> hypogonadism)
ACTH Secreting Pituitary Adenoma
Tumour of pituitary gland
Causes Cushing’s disease (hyperadrenalism)
Generalized Hypopituitarism
Endocrine deficiency syndromes resulting from partial or complete loss of anterior pituitary lobe function.
Generalized Hypopituitarism: Sx
Usually insidious. Depends on hormones affected.
Most commonly GH lost first, then gonadotropins, then TSH and ACTH.
Hyperpituitarism
Overproduction of any of the pituitary hormones
Low gonadotropins: Sx
In kids: delayed puberty
In premenopausal women/ amenorrhea, reduced libido, regression of secondary sexual characteristics, infertility.
In men: erectile dysfunction, testicular atrophy, regression of secondary sexual characteristics, infertility. Decreased muscle mass.
Low GH: Sx
Decreased energy, muscle mass, central obesity, impaired attention and memory.
Usually asymptomatic and clinically undetectable
Low TSH: Sx
Hypothyroidism: facial puffiness, hoarse voice, bradycardia, cold intolerance. Weight gain. Hair loss. Slowed thinking.
Low ACTH: Sx
Hypoadrenalism: fatigue, hypotension, stress and infection intolerance
–> does not result in hyperpigmentation characteristic of primary adrenal failure.
Hypopituitarism: appetite
Can affect appetite (resemble anorexia nervosa or conversely hyperphagia–> obesity)
Low ADH: Sx
Diabetes insipidus.
Extreme thirst, dehydration, hyperatremia.
Low oxytocin
Generally few symptoms if not birthin’ or nursin’
Cushing’s Syndrome
Chronic high cortisol
Excess pituitary production of ACTH, usually secondary to pituitary adenoma.
Cushing’s syndrome: Sx
Moon facies Truncal obesity with thin limbs Buffalo hump Muscle wasting Thin skin Poor wound healing Purple straie
Cushings disease
Cushings syndrome caused by excessive pituitary production of ACTH
ACTH-dependent hyper function of the adrenal cortex can result from:
1 hypersecretion of ACTH by pituitary gland
- Secretion of ACTH by nonputuitary tumour
- Administration of exogenous ACTH
Test to differentiate between pituitary and adrenal hypercortisol disorders.
Dexamethasone suppression test
(Suppresses ACTH release by pituitary; if cortisol levels still high then problem is adrenal).
Central Diabetes insipidus
Neurogenic diabetes insipidus
Low levels of ADH (vasopressin) produced by hypothalamus, or failure or pituitary gland to release it.