pituitary Flashcards

pituitary hormone dysregulation: distinguish between primary and secondary disease states relating to pituitary function, recall the individual pituitary hormone deficiency and excess states that can occur and explain how these are diagnosed and treated

1
Q

5 groups of anterior pituitary hormones

A

FSH/LH (follicle-stimulating hormone, leutinising hormone; both gonadotropins), prolactin (lactation post-partum), GH (growth hormone), TSH (thyroid-stimulating hormone; (make T3 and T4), ACTH (adrenocorticotropic hormone; make cortisol)

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2
Q

what disorder results in a secondary endocrine gland disease

A

when anterior pituitary gland hormone secretion is disordered (still receiving releasing/inhibiting hormone secreted by neurosecretory cells in hypothalamus (median eminence))

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3
Q

what disorder results in a primary endocrine gland disease

A

when endocrine gland (e.g. thyroid, gonads, adrenal cortex to release a primary hormone) is disordered

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4
Q

biochemical diagnosis of hypopituitarism: difficulties of using basal plasma concentrations of pituitary or target endocrine gland hormones

A

interpretation may be limited as pulsatile, undetectable cortisol (at night), T4 with a circulating half-life of 6 days (long half-life), cyclical FSH/LH, pulsatile GH/ACTH

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5
Q

biochemical diagnosis of hypopituitarism: why are stimulated (dynamic) pituitary function tests used and what do they consist of

A

we cause insulin-induced hypoglycaemia (<2.2mM) to stimulate GH and ACTH release, which are stress hormones (go up in terms of stress) so we can measure coristol; give TRH to stimulate and measure TSH and GnRH to stimulate and measure FSH and LH

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6
Q

biochemical diagnosis of hypopituitarism: radiological diagnosis

A

pituitary MRI may reveal specific pituitary pathology e.g. haemorrhage (apoplexy), adenoma; if an empty sella turcica (posterior bright spot on MRI not seen), then only thin rim of pituitary tissue seen as long-term hypopituitarism

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7
Q

replacement and check if ACTH deficient

A

hydrocortisone to mimic pulsatile release (more in morning, then over course of day); serum cortisol

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8
Q

replacement and check if TSH deficient

A

thyroxine; serum free T4 (body can convert to T3)

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9
Q

replacement and check if women LH/FSH deficient

A

HRT (E2 plus progestagen); symptom impovement, withdrawal bleeds

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10
Q

replacement and check if men LH/FSH deficient

A

testosterone; symptom improvement, serum testosterone (must induce sperm induction over short space of time)

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11
Q

replacement and check if GH deficient

A

GH; IGF1, growth chart (children)

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12
Q

define hyperpituitarism

A

excess pituitary hormone secretion

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13
Q

2 casues of hyperpituitarism

A

isolated pituitary tumours, ectopic (from non-endocrine tissue e.g. other tissue with hormone-producing tumour)

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14
Q

what is hyperpituitarism generally often associated with

A

visual field and other e.g. cranial nerve defects; endocrine-related signs and symptoms

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15
Q

effect of pituitary tumour on vision

A

as tumour grows (hyperplasia), it compresses optic chiasm, where fibres from nasal retinae cross (where light from temporal aspects of visual fields strikes), so causes bitemporal hemianopia

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16
Q

assessing bitermporal hemianopia

A

restricted peripheral vision but may present late as can still see enough to navigate; perimetry (flashes on screen and press button when see; all temporal flashes not seen)

17
Q

hyperpituitarism: result of excess of ACTH (corticotrophin)

A

Cushing’s disease

18
Q

hyperpituitarism: result of excess of TSH (thyrotrophin)

A

thyrotoxicosis

19
Q

hyperpituitarism: result of excess of gonadotrophins (LH and FSH)

A

precocious puberty in children

20
Q

hyperpituitarism: result of excess of prolactin

A

hyperprolactinaemia

21
Q

hyperpituitarism: result of excess of GH

A

gigantism (child), acromegaly (adult)

22
Q

what size is a pituitary tumour usually

A

microadenoma (<1cm)

23
Q

what disease can pituitary tumour symptoms be associated with

A

diabetes mellitus