Lecture 3 - Pathology of neurohypophysis, pituitary insufficiency

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clinical manifestations diabetes insipidus

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1

clinical manifestations diabetes insipidus

polyuria, polydipsia, nocturia → chronic fatigue syndrome, bmd decrease

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2

hypertonic dehydration

fever, circ failure, coma

in case of water intake restriction

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3

paracllnical dm insipidus

thirst test - if polydipsia/polyuria

urine/plasma osmolarity

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4

nephrogenic di - forms

hereditary - mutations, in males

acquired - pyelonephritis (+ other kidney diseases), decreased aquaporin 2 (from drugs)

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5

evolution diabetes insipidus

bladder hypertrophy → hydroureter, triphasic evolution pituitary is postop or posttrauma (hyper → hypo → hypernatremia)

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6

treatment DI

desmopressin

adjuvant - in partial forms → carbamazepine, chlorpropamide, clofibrate, indomethacin

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7

treatment nephrogenic di

low salt, hydrochlorothiazide

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8

SIADH characteristics

hyponatremia, plasma hypoosmolarity, high urinary Na+

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9

causes siadh

ectopic production by tumor (carcinomas, thymomas)

drug-induced (drugs for DI like vasopressin, chlorpropamide)

injuries baroreceptor system by lung/cns disease

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10

treatment siadh

chronic - water restriction, correction hyponatremia slowly

hypertonic saline

tolvaptan

urea

slgt2i

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11

osmotic demyelination syndrome occurs due to

quick correction hyponatremia in siadh

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12

ighd causes

hereditary - hormonal deficiencies

anomalies of pituitary dev - septo optic dysplasia, pituitary hypoplasia/aplasia

tumoral - macroadenoma, germinoma, cysts

vasc - infarction pituitary (→ increase size) or sheehan’s (postpartum)

pituitary apoplexy

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13

lethargy, anorexia, weight loss and lack of lactation are signs of

sheehan’s syndrome

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14

clinical manifestations gh deficiency

thin smooth skin, wrinkles on face, overweight, adipose at visceral level, asthenia

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15

clinical manifestations acth deficiency - if acute

vasc collapse + death

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16

clinical manifestations tsh deficiency

signs of thyroxine defiiency

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17

clinical manifestations gonadotrophs deficiency

hypogonadism, infertility, no pubic hair

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18

paraclinicals for ighd

anemia, hypoglycemia, hyponatremia (+ no hyperkalemia), increase ldl, decreased bm density

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19

paraclinicals for acth deficiency

measure cortisol at 8am

insulin tolerance test

acth stimulation test

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20

paraclinicals in gonadotrope deficiency

men - basal testosterone dosage

women if amenorhea - estrogen, lh, fsh

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21

arginine test is for

gh deficiency

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22

treatment acute form of pituitary failure

hydrocortisone iv

levothyroxine

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23

treatment chronic form pituitary failure

hydrocortisone, prednison, l-thyroxine

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24

treatment women w/ gh defieincy

estradiol, progesterone

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treatment men w/ gh deficiency

testosterone

lh, fsh, gnrh for fertility

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26

treatment gh deficiency

recomb gh somatotropin (rhgh)

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27

se somatropin

dm

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28

__ can unmask di by increasing bp and renal flow

glucocorticoid replacement

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29

avp defiicency vs resistance

central di - deficiency

nephrogenic - resistance

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30

_______ has placental enzymes and associated w/ hepatic steatosis, preeclampsia and coagulopathy

gestational di

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31

wolfram syndrome

hereditary central di, optic atrophy and deaf

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32

etiologies central di

  1. tumour

  2. trauma/postop

  3. infilrative - histiocytosis

  4. infectious

  5. vasc

  6. hypophysitis

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