Pituitary disease in small animals Flashcards
Hypersomatotrophism (‘Acromegaly’) - Pathogenesis
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
Hypersomatotrophism - Hx + clinical signs
PU/PD & polyphagic with weight gain
‘thick-set’ facial features
incr interdental spaces
some signs d/t poorly controlled diabetes mellitus -hepatomegaly & cataracts (dogs)
Hypersomatotrophism - diagnostic aids
serum GH estimation
serum IGF1 estimation - useful for dogs, not cats
serum progesterone levels + abdominal ultrasound in dogs
CAT or MRI scan in cats
Hypersomatotrophism - therapy
dogs - remove progesterone influence
cats - dopamine agonists, local irradiation, somatostatin analogues
Hyposomatotrophism (‘Dwarfism’) - pathogenesis
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
Hyposomatotrophism - Hx + clinical signs
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
Hyposomatotrophism - diagnostic aids
serum GH estimation - relatively unavailable
serum IGF1 estimation – possibly valuable in dogs
delayed growth plate closure
Hyposomatotrophism - therapy
none required
consider progestin therapy
Diabetes insipidus - pathogenesis
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
Diabetes insipidus - Hx + clinical signs
marked and unremitting PU/PD
otherwise unremarkable both on history and PE
Diabetes insipidus - diagnostic aids
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
Diabetes insipidus - therapy
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