Endocrinology SA Flashcards
Addisons
Pituitary - lose ACTH
Immune mediated adrenal destruction (glomerulosa)
Hyperthyroidism
Common for cats over 12
Aet - adenomatous hyperplasia of both lobes
Underlying cause not well defined
Hyperthyroidism cats CS, Dx
CS -
Progressive
Weight loss
Hyperactive
PU/PD, tachycardia
Dx -
Palpation
Erythro and macrocytosis
More heinz bodies
Increased ALP, ALT, AST, LDH
Total T4 >90% of cases and to monitor
Free T4 (early cases, less sensitive)
T3 suppression test
Scintigraphy
Hyperthyroidism Tx
Thiamazole - Inh. thyroid hormone synthesis
- check total T4 every 3 months
Carbimazole - Prodrug
Meds - reversible, don’t stop hyperplasia, pre op euthyroidism
Rapid recurrence if not compliant
Sx - uni/ bilateral thyroidectomy
Radioiodine- [] in thyroid hormone cells (best choice normally
SHIM RAD
Severe hyperthyroidism
Huge thyroid tumour size
Intrathoracic Tumour
Multifocal Dz
Resistant to Antithyroid Drug
CKD + Hyperthyroidism
Norm creatinine due to msc loss
Glomerular hyperfiltration
Tx can mask CKD
Thyroid storm - acute thyrotoxicosis
homeostasis overwhelmed with excess thyroid hormone
Dogs hyperthyroidism
Functional tumour
Most common cause -
Iatrogenic 2° to oversupplementation (raw food)
Thyroid hormone
Thyroid produces all T4, 40% T3
T3 and T4 plasma bound (99%)
Unbound thyroid hormone is active
T3 is more potent c.f. T4
Hypothyroidism dogs
T3 and 4 deficiency
Mid-old age
Congenital - thyroid hypoplasia/ aplasia
1°-lymphocytic thyroiditis, idio atrophy
2°-pituitary/ hypothalamus defect, neoplasia/ iatrogenic
Hypothyroidism Dx
Bio+Haemology-
Mild anaemia, hypercholoesterol, Mild up CK,
-increased ALP and ALT
Hrm-
Total/ free T4
Antibody measurement
Dynamic function tests (TSH stim)
Hypothyroidism Tx
Levothyroxine - not with food or v. low bioavailability
CS clear-
Metabolic - weeks
Derm - months
Endocrinopathies
Pituitary dwarfism
Acromegaly
Diabetes insipidus
Hyper/hypo PTH
Insulinoma (Panc)
Gastrinoma (Panc)
Phaeochromocytoma (adrenal)
Hyperaldosteronism (adrenal)
PU/PD Ddx
DI - central, primary, secondary
Osmotic diureses- DM, 1°renal glycosuria, Fanconi’s syndrome, Post-Obst diuresis
Iatrogenic- glucocorticoids, diuretics, levothyroxine, phenobarbitone
Renal medullary wash out- loss of medullary hypertonicity
1° PD - Psychogenic
Def- PD >100ml/kg/day
PU/PD work up
History (rule out iatrogenic)
Physical examination (evidence of renal dz, pyometra…)
Haematology (evidence of pyometra / pyelonephritis?)
Biochemistry (hyperCa? hypoNa? renal disease? diabetes?)
Bile acids (liver disease?)
T4 (hyperthyroidism?)
Urinalysis (diabetes, Faconi’s, renal glucosuria?. Culture to rule out pyelonephritis)
If none of above-
Hypercortisolism, Central DI, Primary NDI, 1° polydipsia
Rule out HAC then do water deprivation test
Pituitary gland hormones
FSH
LH
ACTH
TSH
prolactin
Endorphoins
GH
Pituitary dwarfism
GSD congenital lesion
Failure GH secretion
Proportionate dwarfism
-puppy coat, delayed dentition and growth plate closure
-immature gonads
Dx - routine testing, rule out other causes, IGF-1
Tx- progestagens- induce mammary GH secretion
-Adv effects
Don’t breed from
Acromegaly
Excess GH
Cat- Old male pituitary tumour
Dog- FE, Mammary tissue response to progesterone
Acromegaly pathogenesis
Chronic excess GH
Insulin antagonism-> DM
Anabolic effects (IGF-1)-> Organs, Cartilage, Bone
Acromegaly Clinically, Dx, Tx
Clinical features-
Insulin resistant DM, Prognathism
Excess extremity growth
Dx-
Raised liver Ez, DM, Elevated IGF-1
Tx-
Bitch- OVH/ stop progestagens (bone change irreversible)
Cat- Control DM, hypophysectomy, Radiation of mass
Central DI
Complete or partial deficiency in ADH (arginine vasopressin)
So collecting ducts are impermeable to water
Cause- neo/ trauma/ hypophysectomy sequelae
1°Hyper PTH
Functional parathyroid tumour
So Hyper CA, PU/PD, dystrophic calcification
Dx- High total Ca, high PTH, mass detected
Tx- restore norm Ca levels, Sx mass removal
2° Hyper PTH
Renal 2° Hyper PTH
Nutritional 2° Hyper PTH
Pseudohyper PTH
PTH-rp secreting tumour
-Anal sac adenocarcinama
-lymphoma
-multiple myeloma
Hypo PTH
Failure to produce PTH
1° - immune mediated
2° - Sx
CS- HypoCa signs
-Anxiety, muscle twitch, ataxia, tachycardia, weakness
Dx - low Ca, high PO4, low PTH
Tx-
Emergency- IVFT, IV Ca gluconate (slow, ECG)
Maintenance - Oral Ca and Vit D