Pituitary disease in small animals Flashcards

1
Q

Hypersomatotrophism (‘Acromegaly’) - Pathogenesis

A

incr pituitary gland activity
autonomus production of GH - elevated levels of IGF1 and its binding proteins - induces tissue proliferation & hyperplasia
cats - pituitary tumour
dogs - no reported case of a functional pituitary tumour causing hypersomotrophism - all cases d/t incr GH secretion from mammary tissue
juveniles - incr length of long bones, once growth plates have fused changes confined to soft tissue and flat bones
GH is an insulin antagonist - glucose intolerance + many have diabetes mellitus - difficult to control due to insulin resistance

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2
Q

Hypersomatotrophism - Hx + clinical signs

A

PU/PD & polyphagic with weight gain
‘thick-set’ facial features
incr interdental spaces
some signs d/t poorly controlled diabetes mellitus -hepatomegaly & cataracts (dogs)

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3
Q

Hypersomatotrophism - diagnostic aids

A

serum GH estimation
serum IGF1 estimation - useful for dogs, not cats
serum progesterone levels + abdominal ultrasound in dogs
CAT or MRI scan in cats

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4
Q

Hypersomatotrophism - therapy

A

dogs - remove progesterone influence

cats - dopamine agonists, local irradiation, somatostatin analogues

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5
Q

Hyposomatotrophism (‘Dwarfism’) - pathogenesis

A

decr pituitary gland activity
congenital malformation of the pituitary adenohypohysis or in trophic hormone producing cell lines
decr secretion of GH + TSH.
sometimes decr gonadotrophin secretion
ACTH production is usually adequate and posterior pituitary structure & function remain normal

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6
Q

Hyposomatotrophism - Hx + clinical signs

A

small stature and immature hair coat
changes evident at 6-8weeks - earlier with concurrent hypothyroidism
non chondrodystrophic dwarfism, generally less than 50% normal size
persistent oestrus
normal life expectancy

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7
Q

Hyposomatotrophism - diagnostic aids

A

serum GH estimation - relatively unavailable
serum IGF1 estimation – possibly valuable in dogs
delayed growth plate closure

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8
Q

Hyposomatotrophism - therapy

A

none required

consider progestin therapy

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9
Q

Diabetes insipidus - pathogenesis

A

decr vasopressin secretion from the posterior pituitary
Occasionally secondary to an expanding mass lesion or congenital abnormality - most commonly idiopathic
decr ADH = collecting tubules impermeable to water - urine is persistently & unremmitingly hyposthenuric

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10
Q

Diabetes insipidus - Hx + clinical signs

A

marked and unremitting PU/PD

otherwise unremarkable both on history and PE

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11
Q

Diabetes insipidus - diagnostic aids

A

urine sg < 1.008
biochemical screen to preclude other causes of PU/PD
an inability to concentrate urine with confirmed dehydration; documented by a water deprivation test
marked incr in urine sg after subcutaneous administration of desmopressin
low dose dexamethasone suppresion test to preclude hyperadrenocorticism

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12
Q

Diabetes insipidus - therapy

A

desmopressin nasal spray administered onto the ocular conjunctiva every 12 – 24 hours
injectable desmopressin given subcutaneously every 12 –24 hours
adjust dose on the basis of water consumption, urine conc and body weight

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