EOR endocrine part 2 Flashcards

1
Q

What is the MCC of hyperthyroidism?

A

Graves’ disease

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2
Q

What is Graves’ dz?

A

Diffuse goiter with hyperthyroidism, exophthalmos, and pretibial myxedema

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3
Q

Etiology of Graves’ dz

A

Caused by circulating antibodies that stimulate TSH receptors on follicular cells of the thyroid

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4
Q

Female to male ratio of Graves’ dz

A

6:1

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5
Q

What specific physical finding is associated with Graves’?

A

Exophthalmos

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6
Q

How is the dx made of Graves’ dz?

A

Increased T3, T4, and anti-TSH receptor antibodies
Decreased TSH
Global uptake of I131 radionuclide

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7
Q

Name tx option modalities for Graves’ dz

A

Medical blockade: iodide, propranolol, PTU, methimazole, Lugol’s solution (potassium iodide)
Radioiodide ablation: most popular therapy
Surgical resection: bilat subtotal thyroidectomy

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8
Q

What are the possible indications for surgical resection in Graves’ dz?

A
Suspicious nodule
If pt is noncompliant or refractory to medicines
Pregnant
A child
If pt refuses radioiodide therapy
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9
Q

What is the major complication of radioiodide or surgery for Graves’ dz?

A

Hypothyroidism

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10
Q

How does PTU work?

A

Inhibits incorporation of iodine into T4/T3 (by blocking peroxidase oxidation of iodide to iodine)
Inhibits peripheral conversion of T4 to T3

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11
Q

How does methimazole work?

A

Inhibits incorporation of iodine into T4/T3 only

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12
Q

Define primary hyperparathyroidism

A

Increased secretion of PTH by parathyroid gland(s); marked by elevated calcium, low phosphorous

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13
Q

Define secondary hyperparathyroidism

A

Increased serum PTH resulting from calcium wasting caused by renal failure or decreased GI calcium absorption, rickets, or osteomalacia; calcium levels are usually low

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14
Q

Define tertiary hyperparathyroidism

A

Persistent HPTH after correction of secondary hyperparathyroidism; results from autonomous PTH secretion not responsive to the normal negative feedback due to elevated calcium levels

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15
Q

What are the methods of imaging the parathyroids?

A
Surgical operation
U/s
Sestamibi scan
TI (technitium)- thallium subtraction scan
CT scan/MRI
A-gram (rare)
Venous sampling for PTH (rare)
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16
Q

What are the indications for a localizing preoperative study?

A

Reoperation for recurrent hyperparathyroidism

17
Q

What is MCC of primary hyperparathyroidism?

A

Adenoma (>85%)

18
Q

What are the etiologies of primary HPTH and percentages?

A

Adenoma (~85%)
Hyperplasia (~10%)
Carcinoma (~1%)

19
Q

What are the RFs for primary hyperparathyroidism?

A

FHx
Men-I
MEN IIa
Irradiation

20
Q

What are the s/sx of primary HPTH hypercalcemia?

A

Stones: Kidney stones
Bones: bone pain, pathologic fx, subperiosteal resorption
Groans: muscle pain and weakness, pancreatitis, gout, constipation
Psychiatric overtones: depression, anorexia, anxiety
Other sx: polydipsia, wt loss, HTN, polyuria, lethargy

21
Q

What is the 33-to-1 rule?

A

Most pts with primary HPTH have a ratio of serum chloride to phosphate greater than or equal to 33

22
Q

What plain XR findings are classic for HPTH?

A

Subperiosteal bone resorption

23
Q

How is primary HPTH diagnosed?

A

Labs- elevated PTH (hypercalcemia, decreased phosphorous, increased chloride)
Urine calcium should be checked for familial hypocalciuric hypercalcemia

24
Q

What is familial hypocalciuric hypercalcemia?

A

Familial (autosomal dominant) inheritance of a condition of asymptomatic hypercalcemia and low urine calcium, with or without elevated PTH
In contrast, hypercalcemia from HPTH results in high levels of urine calcium

25
Q

DDx of hypercalcemia

A
Calcium overdose
Hyperparathyroidism
Hyperthryoidism
Hypocalciuric hypercalcemia
Immobility/iatrogenic (thiazide diuretics)
Metastasis/milk alkali syndrome
Paget's disease
Addison's disease/acromegaly
Neoplasm
Zollinger-Ellison syndrome
Excessive vit D
Excessive vit A
Sarcoid
26
Q

What is the initial medical tx of hypercalcemia (primary HPTH)?

A

Medical- IVF, furosemide- NOT thiazide diuretics

27
Q

Although most recommend surgery for asymptomatic primary HPTH, when is it considered mandatory?

A

Renal insufficiency (CR decreased by 30%)
Osteoporosis
Age <50
Calcium >1 mg/dL above upper limit of nl
Hypercalciuria (>400 mg/day Ca excretion)

28
Q

What is the definitive tx for primary HPTH resulting from hyperplasia?

A

Neck exploration removing all parathyroid glands and leaving at least 30 mg of parathyroid tissue placed in the forearm muscles

29
Q

What is the definitive tx for primary HPTH resulting from parathyroid adenoma?

A

Surgically remove adenoma (send for frozen section) and bx all abnormally enlarged parathyroid glands

30
Q

What is the definitive tx for primary HPTH resulting from parathyroid carcinoma?

A

Remove carcinoma, ipsilateral thyroid lobe, and all enlarged LNs

31
Q

What is the definitive tx for secondary HPTH?

A

Correct calcium and phosphate; perform renal transplantation

32
Q

What is the definitive tx for tertiary HPTH?

A

Correct calcium and phosphate
Perform surgical operation to remove all parathyroid glands and reimplant 30-40 mg in the forearm if refractory to medical tx

33
Q

What must be ruled out in the pt with HPTH from hyperplasia?

A

MEN type I and MEN type IIa

34
Q

What carcinomas are commonly associated with hypercalcemia?

A
Breast CA metastases
Prostate CA
Kidney CA
Lung CA
Pancreatic CA
Multiple myeloma