Clinical questions - Endocrinology Flashcards

1
Q

Subacute (de Quervain) thyroiditis

A

Painful goiter

mechanism: granulomatous inflammation of the thyroid presents initially with thyroid pain and hyperthyroidism with release of preformed hormone then becomes transiently hypothyroid before return to euthyroid.

Radioactive iodine uptake scan shows decreased uptake
Initial labs decreased TSH, elevated T4. At 6 months out will be elevated TSH or normal.

Tx with NSAIDs for acute inflammation
Hyperthyroid sis (palpitations, fine tremor in hands): b-blocker (propranolol, atenolol) for a few weeks

No indication for methimazole or propylthiouracil as this is preformed hormone and these block synthesis.

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2
Q

Treatment for Cushing syndrome secondary to exogenous glucocorticoid administration

A

Most common cause

Taper off glucocorticoids

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3
Q

Treatment for Cushing syndrome secondary to Corticotroph pituitary adenoma

A

Elevated ACTH - True Cushings

Transsphenoidal resection +/- irradiation of pituitary

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4
Q

Treatment for Cushing syndrome secondary to hyperfunctioning adrenal adenoma

A

Primary hypercortisolism

Unilateral adrenalectomy

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5
Q

Treatment for Cushing syndrome secondary to ectopic ACTH production from a non-pituitary site

A

i.e. small cell lung cancer

Surgical resection and treatment of underlying tumor
Ketoconazole - suppresses adrenal steroid synthesis
Mitotane - kills adrenal glands
B/l adrenalectomy

followed by hormone replacement if resecting adrenal glands

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6
Q

Management of lactotroph adenoma aka prolactinoma

A

Medical management:
-Dopamine agonist to inhibit secretion of prolactin - can shrink the tumor
>Capergoline, bromocriptine

Surgical management:

  • Transphenoidal resection
  • Indicated if failed medical management or if female with adenoma >3 cm who desires pregnancy
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7
Q

Most appropriate first line treatment for newly diagnosed type 2 diabetes

A

metformin - always give at diagnosis

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8
Q

Risks of supratherapeutic doses of levothyroxine, and management of

A

accelerated bone loss
Arrhythmias - a fib

Mgmt:
Decrease dose
Re-evaluate labs in 6 weeks with appointment

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9
Q

Levothyroxine role in thyroid cancer

A

given after resection for replacement as well as to suppress TSH to keep cancer from growing

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10
Q

Most common cause of hypothyroid

A

Hashimoto thyroiditis - gradual decrease in thyroid hormone levels

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11
Q

Osteoporosis - at risk population and treatment

A

Increased risk: thin, post-menopausal women, whites > asians

Tx:
Bisphosphonates - need to take first thing in the morning with 8 oz of water, no laying down d/t risk of pill esophagitis
Ca + Vit D
Wt bearing exercise at least 3x/wk
fall prevention
avoid smoking and heavy alcohol use
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12
Q

Adrenal crisis - presentation and treatment

A

patient with primary adrenal insufficiency with acute illness, presents with hyponatremia, hyperkalemia (both 2/2 mineralocorticoid deficiency) and hypoglycemia (2/2 glucocorticoid deficiency), can present in shock

Tx:
ICU admission for hemodynamic monitoring
IV dexamethasone
IVF
IV glucose
elytes prn
Tx underling cause

Counsel about stress dose PO steroids during illness and have a vial of hydrocortisone on hand if acutely ill or unresponsive

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13
Q

Work up for a solitary, nontender thyroid nodule

A

1st: labs - TSH/Free T4, Thyroid U/S

If TSH low, T4 high = hyperthyroid
> radioactive iodine uptake scan
» If HOT it’s NOT cancer - treat hyperthyroid
» If Cold get FNA - 10% are cancer

If TSH is normal with T4 normal or TSH elevated with low T4 proceed with FNA
- It is not a hot nodule if the T4 is not high

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14
Q

Pheochromocytoma - preoperative treatment

A

alpha blockade - phenoxybenzamine or phentolamine

Can use labetalol

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15
Q

Diagnoses that should be considered with bilateral phenochromocytoma

A

MEN 2 or VHL disease (Von Hippel Lindau)

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16
Q

Adrenal gland disorders causing secondary hypertension

A

Cushing syndrome

Hyperaldosteronism

17
Q

Triad of findings associated with hyperaldosteronism

A

Hypertension - retaining sodium/water

Hypokalemia - K secretion

Metabolic alkalosis - lose H+ with the activation of the sodium-hydrogen exchange protein in the kidney (aldosterone effect), as well as H-K pump moving intracellular K to extracellular and H intracellularly to promote increased H+ secretion in the kidney to enable increased K+ reabsorption

18
Q

Paget disease of bone

A

Involves axial skeleton and long bones

Present with “hat too tight” due to increased skull thickness

XR with lytic lesions however normal Ca, Phos, Cr, Hgb to r/o multiple melanoma; elevate ALP

Dx: XR, radionuclide bone scan

Tx:
IV or PO bisphosphonate (Zoledronic acid most effective) - inhibits osteoclast activity