L7: Endocrine disorders Flashcards

1
Q

most common cause for acromegaly :

A

benign pituitary GH-secreting adenoma —> elevated growth hormone —> would cause gigantism in adults

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2
Q

acromegaly is associated with which conditions ?

A

increased risk of :
-carpel tunnel syndrome

-obstructive sleep apnea

-type 2 DM or glucose intolerance

-heart disease and hypertension

-arthritis

-bitemporral hemianopsia __>resulting from compression of optic chiasm by pituitary adenoma

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3
Q

lab diagnosis for acromegaly :

A

measure IGF-1 (insulin like growth factor 1), usually increased in acromegaly

confirm diagnosis with oral glucose suppression test
(GH levels will remain elevated despite glucose administration so GH is NOT reliable test )

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4
Q

MRI on a patient suffering from acromegaly shows :

A

sellar lesion

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5
Q

treatment for acromegaly:

A

transphenoidal surgical resection or external beam radiation of the tumor

octreotide (somatostatin analog) is used to supress GH secretion

pegvisomant (GH receptor antagonist ) can be used to block peripheral actions og GH

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6
Q

What is the best test for screening of thyroid disease and for assessment of thyroid function?

A

TSH measurement

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7
Q

what is high TSH associated with ?

A

primary hypothyroidism

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8
Q

what is low TSH associated with ?

A

primary hyperthyroidism

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9
Q

why is total T4 measurement not an accurate screening for thyroid function and free T4 measurement is preferred ?

A

becasue 99% of circulating T4 is bound to thyroxine-binding protein and total T4 levels can be altered by changes in levels of binding proteins

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10
Q

most common cause of hyperthyroidism :

A

graves disease : autoimmune form of hyperthyroidism

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11
Q

clinical presentations of hyperthyroidism :

A

patient presents with :
-weight loss
- heat intolerance
-anxiety
-palpitations
-increased bowel frequency
-insomnia
-menstrul abnormalities

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12
Q

examination of patent with hyperthyroidism reveals :

A

moist skin
-goiter
-sinustachycardia
-atrial fibrillation
-fine tremor
-lid lag
-hyperactive reflexes

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13
Q

characteristic features of hyperthyroidisim of graves disease only ( not present in other type of hyperthyroidism)

A

exophthalmos

pretibial myxedema

thyroid bruits

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14
Q

treatment for hyperthyroidism :

A

symptomatic treatment :
- propranolol to manage androgenic symptoms

-anti-thyroid drugs :
-methimazole or propylthiouracil

-thyroidectomy (levothyroxine T4 replacement administered if this is the case )

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15
Q

how does thyroiditis affect thyroid hormone secretion ?

A

inflammation of thyroid gland causing release of previously synthesized thyroid hormone resulting in temporary hyperthyroidism phase followed by hypothyroidism

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16
Q

what is thyroid storm ?

A

acute life threatening form of thyrotoxicosis

-urgent treatment with IV propranolol ,PTU , and corticosteroid

high dose of potassium iodide (SSKI) is also effective

17
Q

most common cause for hypothyroidism :

A

Hashimoto’s thyroiditis (autoimmune hypothyroidism )—> associated with antithyroglobulin and ant microsomal (anti-TPO) antibodies that precipitate thyroid destruction

18
Q

clinical features of hypothyroidisim :

A

patient presenting with :
-weakness
-fatigue
-cold intolerance
-constipation
-weight gain
-depression
hair loss
-menstural irregularities

examination reveals:
-cold, puffy skin
-edema,
- bradycardia
-delayed relaxation of deep tendon reflexes such as ankle jerk

19
Q

what is a myxedema coma ?

A

severe hypothyroidism with decreased mental status , hypothermia , and other parasympathetic symptoms—-> treat with IV levothyroxine and IV hydrocortisone if adrenal insufficiency has not been excluded

20
Q

hyperactivity disorders of adrenal gland :

A

-Cushing’s syndrome
-hyperaldosteronism
-adrenogenital syndrome

21
Q

hypoactivity disorders of adrenal gland :

A

-chronic adrenal insufficiency (Addison’s disease )
-acute adrenal insufficiency
-congenital adrenal hyperplasia

22
Q

Cushing’s syndrome results from :

A

elevated serum cortisol levels
-most frequently from iatrogenic prolonged treatment with exogenous corticosteroids

23
Q

what is the most common endogenous cause of Cushing’s syndrome ?

A

hypersecretion of ACTH from pituitary adenoma

24
Q

presenting features of cushings syndrome :

A

patient pressents with :
-HTN
-T2DM
-depression
‘-weight gain
-muscle weakness
-easy bruisability
-increased susceptibility to infection
-psychological disturbances
-hirsutism
-central obesity
-moon face
-baffalo hump
-purple striae

25
Q

diagnosis of cushings syndrome :

A

1,) elevated 24 hour free urine cortisol

2.) elevated midnight salivary cortisol level on 2 separate night

3.) 1mg dexamthasone suppression test + is AM cortisol is persistently elevated the morning after administration of dexamethasone

26
Q

if lab tests suggest Cushing’s disease what should be ordered?

A

pituitary MRI

27
Q

How can you differentiae between ACTH dependent (pituitary/ectopic) and ACTH independent causes?

A

Measure morning (8:00am) cortisol and ACTH levels. If ACTH is elevated, Cushing’s disease or ectopic ACTH is likely.

28
Q

adrenal imaging should be ordered when :

A

only if the work up suggests ACTH-independent etiology (high risk of adrenal incdentalomas)

29
Q

treatment for cushings syndrome :

A

surgical resection of source

inhibitors of adrenal steroigogenesis in case of bilateral adrenal hyperplasia

permenant hormone replacment therapy

30
Q

destruction of adrenal cortex leading to glucocorticoid (cortisol)
and mineralocorticoid (aldosterone) deficiency :

A

addisons disease(usually autoimmune)

-other causes:
TB
adrenal metastases
lymphoma
HIV
adrenal hemorrhage

31
Q

adrenal disease cauing hyperpigmentation:

A

addisons disease

32
Q

diagnosis of addisons diseas:

A

-hyponatremia
-esionophillia
-hyperkalemia
-hypercalcemia
-confirmed by 8 am plasma cortisol level test and synthetic ACTH stimulation test

failure of cortisol to rise >18ug/dl following ACTH administration confirms diagnosis

33
Q

primary treatment of Addison’s disease:

A

glucocorticoid and mineralocorticoid replacement therapy

34
Q

secondary / tertiary treatment of Addison’s disease:

A

only glucocorticoid replacement is necessary (mineralocorticoid production is not ACTH dependent )

35
Q

treatment of adrenal crisis :

A

IV steroids to correct electrolyte abnormalities

50% dextrose to correct hypoglycemia and initiate aggressive volume resuscitation

36
Q

how should chronic steroid therapy be stopped ?

A

tapered slowly to avoid secondary / tertiary Addison’s disease

37
Q

subacute forms of thyroditis present with :

A

tender thyroid , malaise , URI symptoms

all others are associated with painless goiter

38
Q

treatment for thyroditis :

A

beta blockers for hyperthyroidism

levothyroxine for hypothyroidism

for severe cases : NSAID or oral corticosteroid