Endocrine Flashcards

1
Q

Most common cause hyperpituitarism

A

adenoma ant lobe
GNAS1 most common mutation

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2
Q

Morphology pituitary adenoma

A

cellular monomorphism
absence reticulin network

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3
Q

Percentage loss for symptomatic hypopituitarism

A

75% parenchyma

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4
Q

main cause ectopic ADH secretion

A

small cell carcinoma lung

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5
Q

Most common cause hyperthyroid

A

85% graves - diffuse hyperplasia
multinodular goitre
thyroid adenoma

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6
Q

Hashimotos

A

10x more women
autoimmune destruction thyroid gland
assoc other autoimmine and marginal zone b cell lymphoma thyroid

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7
Q

granulomatous (de quervians) thyroiditis

A

painful
triggered by viral infection
multinucleate giant cells
transient hyperthyroid
no radioiodine uptake

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8
Q

Graves

A

most common cause hyperthyroid
90% have thyroid stimulating immunoglobuln
Anti tsh ab

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9
Q

diffuse non toxic goitre

A

enlarged follicles filled with colloid
main cause iodine deficiency
euthyroid

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10
Q

Signs of thyroid neoplasm

A

solitary nodule
young male
previous radiation head / neck
takes up radioiodine

capsular and vascular invasion

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11
Q

Most common thyroid cancer

A

papillary > follicular > medullary > anaplastic

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12
Q

hypercalcaemia in malignancy

A

more likely to be symptomatic
from rankl activating osteoclasts
PTHrP from squamous cell carcinoma

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13
Q

main cause hypercalcaemia

A

primary hyperthyroid - adenoma

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14
Q

Cause of death DM

A

MI then renal

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15
Q

T1DM immunological and genetic

A

destruction of beta cells by T lymphocytes
Class II MHC on chormosome 6
95% have HLA DR3 or DR4
viruses - cocksackie B, MMR, CMV, mono

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16
Q

MEN1 syndrome

A

Pancreas Pituitary Parathyroid
assoc insulinoma and zollinger ellison (ulcers inc jejenum)

17
Q

Main causes hypercorisolism

A

main exogenous - steroids
non exogenous 70% pituitary microadenoma (cushings disease)
10 ectopic ACTH e.g. small cell carcinoma lung
10 adrenal adenoma
10 adrenal carcinoma

18
Q

Dexamethasone suppression test

A

in cushings disease small dose makes no difference, large dose suppresses ACTH and thus urinary steroids decreased

19
Q

Causes primary hyperaldosteonism

A

60% bilateral idiopathic
35% adenoma (conns)
or carcinoma

20
Q

CAH

A

autosomal recessive
main cause 21 hydroxylase deficiency
ciculatory collapse and virulisation

21
Q

waterhouse friedrichson syndrome

A

bilateral adrenal haemarrhage
caused by sepsis normally n meningitides
DIC and widespread purpura
circulatory collapse and death witout steroids

22
Q

Main causes addisons

A

autoimmune adrenalitis with ABs against IL17, 21 and 17 hydroxylase
TB
Aids
Metastatic Ca

23
Q

secondary adrenocortical insufficiency

A

pituitary
decreased sex hormones an cortisol but aldosterone maintained
no change in skin pigmentation

24
Q

Syndromes assoc adrenocortical neoplasms

A

li fraumeni 9TP53), beckwit wiedermann

25
Q

Phaeochromocytoma rule of 10s

A

10% extra adrenal
10% of sporadic bilateral
10% malignant
10% not assoc increased BP

26
Q

Acidophil cells

A

progenitors for both GH-producing somatotrophs and prolactin-producinglactotrophs

27
Q

Twin concordance T2DM

A

Up to 80%