Endocrine Flashcards

1
Q

Hypothyroid: Hashimotos Thyroiditis

A
  • increased risk of Non Hodgkins Lymphoma (if suspected Large needle biopsy)
  • moderately enlarged non tender thyroid
  • may be hyperthyroid prior to hypothyroid
  • ***Antimicrosomal antibodies- (Anti-TPO) **
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2
Q

Hypothyroid: Subacute Thyroiditis

A
  • self limited following flu like illness/viral illness
  • findings: elevated ESR, jaw pain and very tender thyroid.
  • due to release of preformed hormones (low radioiodine uptake) therefore antithyroid drugs will not work
  • Raiu is low, t4 high, TSH low
  • Tx: NSAIDS and Bblockers
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3
Q

Hyperthyroid: Graves

A
  • autoimmune hyperthyroidism with thyroid stimulation TSH receptor antibodies
  • findings: enlarged smooth non tender thyroid,
  • increased radioiodine uptake
  • Tx: radioactive iodine ablasion
    if opthalmoplegias then pretreat with glucocorticoids to prevent worsening
    in pregnancy use PTU (1st Trimester) Methimazole (2nd Trimester)
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4
Q

Hyperthyroid: Thyroid Storm

A
  • stress induced catecholamine surge
  • dx is clinically made
  • glucocorticoids decrease T4–>T3 transition
  • Other TOC: methimazole, PTU, propanolol
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5
Q

Hypothyroid: Postpartum

A
  • painless
  • release of preformed thyroid hormone
  • decrease radioactive uptake of thyroid hormone
  • may have positive Anti TPO antibodies
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6
Q

Thyroid Cancer: Papillary

A
  • MC and excellent prognosis
  • Tx: total thyroidectomy + radioactive iodine uptake followed by total body imaging to check for uptake
  • levothyroxine is used to suppress TSH to below normal levels
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7
Q

Thyroid Cancer: Follicular

A
  • good prognosis, slow progressing and palpable nodules
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8
Q

Thyroid Cancer: Medullary

A
  • from parafollicular c-cells which produce calcitonin,
  • Associated with MEN2 (link with pheo therefore measure metanephrine)
  • associated with RET protooncogene
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9
Q

Thyroid Cancer: lymphoma

A
  • RF is Hashimotos
  • rapid enlargement is seen
  • Pemberton Sign: presence of facial plethora or neck vein distention when arms are raised which confirms enlarged thyroid gland as cause of eosphageal obstructive symptoms.
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10
Q

Pheochromocytoma:

A
  • associated with MEN 2 and medullary thyroid cancer
  • look for urine metanephrine
  • tx with phenoxybenzamine (alpha blocker) for 10-14 days prior to surgery
  • also encourage increase intravascular compartment
  • hypotension during surgery is common and responds to NS bolus followed by NS infusion
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11
Q

MEN II:

A
  • RET proto-oncogene mutation

* ** medullary thyroid cancer, pheochromocytoma, hyperparathyroidism***

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12
Q

MEN I:

A
  • hyperparathyroidism, gastrinoma, pituitary tumor**
  • mutation of tumor suppressive Menin I
  • gastrinoma (zollinger ellison)
    tx: parathyroidectomy (3.5 glands)
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13
Q

Hyperparathyroid: Primary

A

Primary hyperparathyroid: adenoma, hyperplasia at level of paraythyroid hormone

  • moans, groans and stones ( kidney stones, constipation and bone pain)
  • inc. Ca, dec. Phosp, Inc. PTH
  • indications for surgery: Symptomatic patient, asymp and ca>1 over upper limit of normal, Cr<2.5.
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14
Q

Hyperparathyroid: Secondary

A

Secondary Hyperparathyroidism: due to chronic hypercalcemia, kidney dysfunction, vitamin D deficiency

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15
Q

Hypercalcemia

A

Causes: 1. primary Hyperparathyroid 2. Malignancy (PTHrP)(generally very high Ca levels) 3. Vitamin D induced
Parathyroid Dependant: prim or tert hyperparathyroid, lithium dep, famil hypocalc, hypercalce.
Parathyroid Independant: maligna, vit D tox, granulom disease, milk alkali syndrome

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16
Q

Hyperaldosterone:

A

Primary: due to hyperplasia or adenoma
( elevated aldosterone, low renin)
Secondary: Renal artery stenosis
(High aldosterone and high renin)