Endocrinology Flashcards

1
Q

Most common cause of secondary adrenocortical insuffiency (pituitary failure of ACTH secretion)

A

Sudden exogenous glucocorticoid use cessation without a taper

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2
Q

Addison Disease definition

A

Primary chronic adrenocortical insufficiency, due to adrenal gland destruction causing lack of cortisol and aldosterone, most commonly autoimmune in origin, will see hyponatremia, hyperkalemia, appetite loss, weight loss, nausea, vomiting, hypotension, salt craving, diarrhea

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3
Q

What causes hyperpigmentation in addison’s disease?

A

Excess ACTH release trying to stimulate non responsive adrenal glands

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4
Q

Screening for addison disease

A

High dose ACTH Cosyntropin stimulation test demonstrating an insufficient or absent rise in serum cortisol in response to administration

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5
Q

Most common cause of addisonian crisis

A

Abrupt withdrawal of glucocorticoids without taperring

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6
Q

Cortisol levels should increase to what levels in response to stress?

A

3x basal limits

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7
Q

cushing’s syndrome definition

A

Signs and symptoms related to cortisol excess due to 1 of 4 main causes

1) long term high dose glucocorticoid therapy (most common cause overall)
2) cushing’s disease (most common endogenous cause, pituitary gland ACTH overproduction)
3) Ectopic ACTH producing tumor like small cell lung cancer or medullary thyroid cancer
4) Adrenal tumor

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8
Q

Most specific screening test for cushing’s syndrome

A

24 hr urinary free cortisol

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9
Q

Screening test to differentiate cushing’s syndrome from cushing’s disease?

A

Overnight Dexamethasone suppression test demonstrating suppression of cortisol defines cushing’s disease

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10
Q

Cushing disease definitive management

A

Transsphenooidal surgical resection

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11
Q

Primary hyperaldosteronism as a secondary cause of hypertension

A

Suspected in patients who develop hypertension at extremes of age (<30 or >60 year) or are not controlled on 3 blood pressure meds, may see triad of hypertension plus hypokalemia plus metabolic alkalosis (H+ ions and K+ ions being lost while retaining Na+)

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12
Q

Screening test for primary hyperaldosteronism

A

Plasma renin and aldosterone levels

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13
Q

Drugs to manage primary hyperaldosteronism (2)

A

Spirinolactone, ACE inhibitors

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14
Q

Most common clinical manifestation of a pheochromocytoma

A

Hypertension, may also see headache (most common symptom)

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15
Q

Lab testing for pheochromocytoma

A

Plasma fractionated metanephrines confirmed by 24 hour urinary fractinated catecholamines

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16
Q

Preop management for a pheochromocytoma

A

Non selective alpha blockade PHEnoxybezamine or PHEntolamine 1-2 weeks followed by B blockers or Ca2+ channel blockers to control blood pressure prior to surgery

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17
Q

Hypertensive crisis due to pheochromocytoma immediate management

A

Phentolamine, nitroprusside, or nicardipine

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18
Q

Definitive management of pheochromocytoma

A

Complete adrenalectomy after 1-2 weeks of medical pre op management

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19
Q

TSH receptor Ab vs anti thyroid peroxidase Ab

A

Speciic for graves vs specific for hashimoto’s thyroiditis

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20
Q

2 thyrotoxic medications

A

Lithium and amiodarone

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21
Q

Menstrual flow and thyroid disorders

A

Menstrual flow is decreased in hyperthyroidism (contrary to what you might think), and increased in hypothyroidism

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22
Q

Cretinism definition

A

Untreated congenital hypothyroidism, often due to lack of maternal iodine intake in developing countries or dysgensis of thyroid gland in developed countries, see mental developmental delays, symptoms of hypothyroidism, goiter symptoms, macroglossia, congenital malformations, managed with levothyroxine replacement

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23
Q

Subclinical hypothyroidism definition

A

Isolated increased TSH with normal T4/T3 in patients with few or no symptoms of hypothyroidism, managed conservatively with observation or low dose levothyroxine

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24
Q

Euthyroid sick syndrome definition

A

Abnormal thyroid funciton tests in patients with normal thyroid function, most commonly seen in severe non thyroidal illness, management focused on treating the underlying illness, thyroid hormone replacement usually not indicated

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25
Q

Myxedema coma management

A

IV thyroid hormone replacement plus supportive care and ICU admission, IV glucocorticoids often given

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26
Q

Manifestations of subacute thyroiditis

A

Viral illness followed by hyperthyroidism symptoms initial presesntation, followed by euthyroidism, followed by hypothyroidism, followed by return to baseline, painful thyroid gland aggravated with movements or swallowing (acute neck pain)

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27
Q

Diagnosis of subacute thyroiditis, what about the management?

A

High ESR with negative thyroid antibodies, managed with supportive care as self limiting

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28
Q

Most common therapy to treat graves disease (toxic diffuse goiter)

A

Radioactive iodine to ablate thyroid

29
Q

Purpose of methimazole or propylthiouracil in graves disease***

A

May be used prior to more definitive treatment like thyroidectomy or radioactive iodine, methimazole preferred unless PREGNANT OR THYROID STORM*** then propylthiouracil preferred

30
Q

Toxic adenoma definition

A

Multiple functioning autonomous nodules of the thyroid that can cause signs of hyperthyroidism and can be diagnosed with a radioactive iodine uptake scan demonstrating hot nodules, managed definitively with radioactive iodine ablation

31
Q

Suppurative thyroiditis definition

A

Bacterial infection of the thyroid gland, very rare and usually occurs in children and demonstrates thyroid pain and tenderness, fever, chills, pharyngitis, overlying erythema of skin, leukocytosis on labs and FNA yielding gram stain findings, managed wih antibiotics or surgical drainage

32
Q

Thyroid storm management

A

Propranolol, propylthiouracil, IV glucocorticoids

33
Q

Most common type of thyroid cancer and how is it treated?

A

Papillary thyroid carcinoma, treated with thyroidectomy followed by post op levothyroxine replacement

34
Q

Medullary thyroid carcinoma definition

A

Thyroid tumor derived from calcitonin synthesizing parafollicular C cells, sees increased calcitonin and decreased blood Ca2+ level, managed with total thyroidectomy

35
Q

If TSH is normal or high in a patient with a thyroid nodule, what is indicated? What if TSH is low?

A

FNA with biopsy, radioactive iodine uptake scan with cold nodules being biopsied to rule out malignancy

36
Q

Most common presentation of type I diabetes

A

Hyperglycemia without acidosis (polyuria, polydypsia, polyphagia)

37
Q

Second most common presentation of type I diabetes

A

Diabetic ketoacidosis

38
Q

Greatest risk factor for type II DM

A

Obesity

39
Q

Gold standard for diagnosing DM

A

Fasting plasma glucose > or = 126 blood sugar fasting at least 8 hours on 2 occasions

40
Q

Normal HbA1c vs prediabetic vs diabetic

A

5.6 or or = 6.5

41
Q

Screening for diabetes

A

All adults >45 years every 3 years or any adult with BMI >25 and one additional risk factor every 3 years

42
Q

Name a biguanide

A

Metformin

43
Q

Metformin side effects

A
  • Diarrhea and GI upset

- Lactic acidosis

44
Q

Sulfonyureas mechanism of action and name

A

Stimulate insulin release from pancreatic beta cells, Gly- or Gli-

45
Q

Meglitinide mechanism of action and name

A

Stimulate insulin release from pacnreatic beta cells, -glinide

46
Q

What blood sugar agent is safest in patients with chronic renal disease

A

Repaglinide (metformin is metabolized by liver and kidneys so contraindicated in severe disease of either)

47
Q

Thiazolidinediones mechanism of action and name

A

Increase insulin sensitivity at peripheral receptor sites leading to increased glucose absorption and utilization, no impact on pancreatic beta cells, -glitazone

48
Q

GLP-1 receptor agonist mechanism of action and name

A

Mimics incretin effect leading to increased glucose dependent insulin secretion from beta pacnreas cells, administered via injection except semaglutide (rybelsus), associated with weight loss, -tide

49
Q

DPP4 inhibitors mechanism of action and name

A

Increase GLP-1 levels which therefore mimic incretin effect leading to increased glucose dependent insulin secretion from beta pancreas cells, -gliptin

50
Q

Somogyi phenomenon definition

A

Nocturnal hypoglycemia followed by rebound hyperglycemia in the morning, see night sweats and nightmares and such

51
Q

Dawn phenomenon

A

Rise in serum glucose levels between 2am and 8am requiring reduction of early morning hyperglycemia to control levels consistently

52
Q

Hypoglycemia blood glucose level

A

<70 mg/dL

53
Q

Way to differentiate between endogenous insulin overproduction causing hypoglycemia vs exogenous insulin over administration?

A

C peptide levels which only are elevated with endogenous insulin production

54
Q

Kussmaul respirations

A

Deep rapid continuous respirations

55
Q

Management of DKA and HHS

A

Saline, insulin, K+ repletion, when glucose <250 add D5 saline to prevent hypoglycemia

56
Q

DKA serum glucose vs HHS

A

DKA is between 250-600, HHS will be greater than 600

57
Q

Most common type of diabetic neurpathy

A

Symmetric polyneurpathy involving progressive distal sensory loss in a stocking glove pattern involving distal lower extremities first

58
Q

Most common cause of end stage renal disease

A

Diabetic nephropathy

59
Q

First sign of diabetic nephropathy

A

Microalbuminuria

60
Q

Management of mild vs severe SIADH

A

Mild water restriction, severe IV hypertonic saline plus furoseminde

61
Q

Rapid correction of SIADH can lead to what condition

A

Central pontine myelinolysis

62
Q

SIADH leads to ___natremia while Diabetes insipidus leads to ___natremia

A

Hypo, hyper

63
Q

Lab to diagnose diabetes insipidus

A

Fluid deprivation test, desmopressin stimulation test distinguishes central from nephrogenic

64
Q

Management of central DI vs nephrogenic DI

A

Desmopressin DDAVP first line vs HCTZ

65
Q

Management of moderate hypercalcemia (most often caused by hyperparathyroidism)

A

IV fluids initially, IV loop diuretics can be added to promote calcium excretion, bisphosphonates

66
Q

Chvostek and trousseau’s sign indicate….

A

hypocalcemia

67
Q

Management of severe or symptomatic hypocalcemia

A

IV calcium gluconate

68
Q

Most common type of pituitary adenoma and what are the manifestations and what is the management

A

Prolactinoma, manifests in women with oligomenorrhea, amenorrhea, infertility, galactorrhea rarely, and hypogonadism in med, inferitlity, decreased libido, erectile dysfunction, dopamine agonists like cabergoline or bromocriptine, watchful waiting employed if asymptomatic, transphenoidal surgery possibly

69
Q

Metabolic syndrome 3 of 5 diagnostic criteria

A
  • Decrease HDL
  • Increased blood pressure
  • Elevated fasting triglyceride levels
  • Elevated fasting blood sugar
  • Abdominal obesity