Hyposecretion of anterior pit Flashcards

1
Q

What are the 5 anterior pituary hormones?

A

FSH/LH, TSH, GH, Prolactin, ACTH

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2
Q

In endocrine terms, explain the terms primary and secondary diseases?

A

The chain of command is Hypothallamus->Pit->Endocine gland
Problems with the gland-primary
Problems with the Pit-secondary
Problems with Hypothalamus-tertiary

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3
Q

What is Panhypopituarism?

A

Lose all pituary hormones

Rare to be born without a Ant Pit

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4
Q

What are the signs and causes of congenitale panhypoputuarism?

A

Usually genetic-caused by lack of GH and others in development
short stature and small pit gland on imagine

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5
Q

What are the causes of acquired panhypopituarism?

A
Tumours-hypothalamus/pituary
Radiations-damage (GH most vulnerable, TSH resistant)-can be caused by radiotherapy
Infections (eg:meningitis)
Traumatic brain injury
Infiltrative disease with stalk
Inflammatory-hypophytitis-AID
Piturary apoplexy (heamorrhage/infartion)
sheerans syndroms
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6
Q

What are the signs and presentations of panhypopituarism?

A

Occasionally Simmons disease-
Relevant to deficiency. If lack:
FSH/LH: Secondary Hypogonadism (low libido, erectile dysf, amenhorroa)
ACTH-Secondary hypoadrenalism (no cortisol)-fatigue, death
TSH-secondary hypothyroidism-tired and others
Sheehan’s syndroms

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7
Q

What is Sheehans syndrome?

A

Specifically describes post-partum hypopituitary damage secondary to hypotension after post partum haemorrhage
Pregnant women have bigger AntPit (need more blood) (for prolactin)-so if heamorrhage, not enough blood comes to the AntPit, and it dies off (infarction)
PostPit is usually fine
Causes: Lethargy, anorexia, weight loss, (TSH/ACTH/GH), failure of lactation, failure to resume periods

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8
Q

What is pituary apoplexy? Causes and signs?

A

Intrapituitary haemorrhage or infarction
Often patients have pre-existing Pit tumours
Can be 1st presentations of adenomas
Can be precipitated by Anti-coagulants
Excruciating Headache, visual field defect (compress optic chiasm->Bitemproal Hemianopia (lose exterior vision)
Can also squash cranial nerves

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9
Q

What are the biochemical and radiological diagnosis methods of Hypopituiarsim?

A

1) Basal plasma conc of pit/target endocrine gland hormones-but very limited because these vary during the day (like cortisol), or T4 has a long half live, FSH/LH are cyclical, etc
So prefer:
2) Stimulated pituary function tests
ACTH and GH-in response to stress (Like hypoglyceamia (<2.2 mM)-makes large amounts
TRH/GnRH also can be given to make TSH. FSH/LH
3) radio-Pituatary MRI-reveals pit pathology (hemorrrhage, adenoma, empty sella (long term hypopit)

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10
Q

What replacement hormones can you give for therapy of hypopit?

A

ACTH-Hydrocortisone (check serum cortisol)
TSH-Thyroxine-serum free T4
Women LH/FSH -HRT (E2 and progesteran)-symptoms
Men LH/FSH -Testosterone-symptom improvements
GH-GH-check IGF1 and growth (in children)
One issue is that drugs cant mimic the timing/modulations of these hormones-cant quite give them same QOL as before)

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11
Q

Describe causes and symptoms Somatotrophin deficiency

A

In children-pathologically short (2SD lower than the charts/or drastic stop of growth)
in adults, effects unclear
-> present with lean mass, increased adiposity, increase Waist/Hip ratio, reduced strength?, Cholesterol profile wrong Feel bad => should resolve with treatment

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12
Q

WHat are some causes of Short stature?

A

Causes: Genetic (down syndrome, turners, PW-affects hypothylamus/GHRH)
Emotional deprivation, Systemic disease (CF, arthiritis), Malnutrition, Malabsorption (coeliac), Endocinre-cushing, Hypothry, GH, dwarfism (different ones-can be bones, can be LARON-shit GH receptors)

All in all-impact the growth pathway (GHRH, GH, GHR)
In adults usually caused by trauma
Do provocative challenge (stimulated test (Insulin, or GHRH+Arg, Glucagon, Exercise) -Cut off is not reaching 3mcg/L

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