Acromegaly Flashcards

1
Q

what is this due to

A

increased secretion of growth hormone from pituitary tumour or hyperplasia

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2
Q

where could ectopic GH releasing hormone come from

A

carcinoid tumour

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3
Q

what does GH stimulate bone and soft tissue growth via

A

insulin like growth factor-1

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4
Q

symptoms

A

acroparaesthesia (of digits), amenorrhoea, decr libido, headache, incr sweating, snoring, arthralgia, backache

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5
Q

signs

A

incr growth of hands, jaw and feet; coarsening face, wide nose; big supraorbital ridges; macroglossia; widely spaced teeth; puffy lips, eyelids and skin; scalp folds; skin darkening; acanthosis nigricans; laryngeal dyspnoea; OSA; goitre; proximal weakness and arthropathy; carpal tunnel signs

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6
Q

complications

A

may present with CCF or ketoacidosis. impaired glucose tolerance; vascular- incr bp, LVH, cardiomyopathy, arrhythmias, IHD, stroke. neoplasia- incr colon cancer risk, colonoscopy

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7
Q

tests

A

incr glucose, incr calcium, incr phosphate.

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8
Q

why can you not rely on random GH

A

because secretion is pulsatile and during peaks there is overlap

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9
Q

when can GH increase

A

stress, sleep, puberty, pregnancy

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10
Q

what happens normally with a high glucose

A

suppression of GH and GH hardly detectable. in acromegaly GH fails to suppress

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11
Q

when is an oral glucose tolerance test needed

A

if basal GH >0.4ug/L and/or IGF-1 incr

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12
Q

when is acromegaly confirmed with oral glucose tolerance test

A

if lowest GH during the test is >1ug/L then acromegaly is confirmed

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13
Q

what is the method in OGTT

A

collect samples for GH glucose at 0,30,60,90,120,150 min

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14
Q

when can you get false positives

A

pregnancy, puberty, hepatic and renal disease, anorexia nervosa, DM

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15
Q

other tests

A

MRI of pituitary fossa, look for hypopituitarism, visual fields and acuity, ECG, echo

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16
Q

treatment

A
  1. trans sphenoidal surgery. 2. somatostatin analogues and or radiotherapy eg octreotide or laneotide. 3. GH antagonist- pegvisomant