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51 Cards in this Set

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Look at thyroid anatomy
Superior thyroid arteries from external carotid
Inferior thyroid arteries from thyrocervical trunk
Thyroid IMA from Aorta
Veins drain into internal jugular
RLN relations and functions
What is foramen cecum
Point of attachment of the thyroglossal duct and is formed during embryological descent of thyroid gland.

Thyroglossal duct cysts can form anywhere along this descent.
What does the Recurrent Laryngeal Nerve do?
It is off of the vagus.

Provides motor and sensory to the larynx.
Function of the Thyroid?
Produces T3 and T4 in response to TSH.

It is the thermostat.

More T4, but activity is in T3.
Peripheral conversion of T4--> T3
What is hypothyroid?
Treatment?
Low T3, T4,
High TSH

Tx: Synthroid, Iodine.
No role for surgery!
MC hyperthyroid disease? Description?
Graves.

Goiter, exothalmos (from fat buildup behind eyes), wt loss, heat intolerance.
Diffuse I131 uptake.

Often self limiting, but can take up to 5 yrs.
Treatment for hyperthyroid?
I131,
Beta blockers,
Anti-thyroids (PTU),
Subtotal or total surgery.
What is toxic goiter?
2nd mcc hyperthyroid
Diffuse I131 uptake
Treatment for toxic goiter?
I131,
Beta blockers,
anti-thyroid meds,
Surgery
A few other causes of need for surgery due to hyperthyroidism?
Solitary Toxic Nodule: "hot" on I131 imaging.

Thyroiditis: Hashimotos, DeQuervain, Riedel's Struma

All need partial or subtotal thyroidectomy
Work up of a solitary nodule found on exam?
US - cyst or solid, fine needle aspiration.
I131 scan: hot or cold nodule? (hot-dark, prob ok. cold -ligther, usually bad, maybe cancer)
T4, TSH
Exploration w/ lobectomy AT LEAST.
Treatment for thyroid storm?
Beta blockers and PTU PREOP!!
MCC thyroid cancer?
Papillary carcinoma. 70% thyroid ca.
W>M. 30-40 age group.
Predominant type in kids w/ thyroid cancer and in pts w/ previous radiation to head and neck.
Relatively slow growing, not usually primary ca that kills, usually mets do.
Treatment of Papillary Carcinoma of thyroid?
Lobectomy is usually sufficient UNLESS;
Extremes age,
Tumor >2 cm
In those cases do complete thyroidectomy!

I131 ablation postop
Follicular Carcinoma of Thyroid
10% thyroid cancers.
Angioinvasive, spreads widely via circulatory system, as opposed to lymphatics.
CV much faster spread than lymph!
Treatment for follicular carcinoma of thyroid?
Total thyroidectomy.

I131 ablation postop
Medullary cancer of thyroid?
7%.
May be hereditary, MEN IIa: neural crest
Parafollicular C cells which make calcitonin (decreases calcium level). Not really thyroid, so NO I131 ablation!
Treatment for medullary cancer of thyroid?
Total thyroidectomy.
No chemo.
Check rest of family! If they have high calcitonin, possible they have the same cancer. Can also check Ret proto-oncogene.
What is Anaplastic Thyroid Cancer?
Aggressive cancer. Often invades surrounding areas like the trachea, so often end up doing tracheostomy.

Median survival is 4 months.
Look at parathyroid anatomy

Slide 16 shows embryologic origination of glands.
2 pairs, upper and lower.
Upper from 4th pharyngeal pouch,
Lower form 3rd pharyngeal pouch (longer descent, more variable location).

All arteries from inferior thyroid artery.
All veins drain into internal jugular.
Function of parathyroid glands
Produce PTh to regulate calcium and phos.
In response to LOW calc, PTh:
- releases calc from bones,
- increases calc absorption and phos excretion from kidneys.
- increases calc uptake from gut.
PTh is opposed by calcitonin.
Signs/Sx of HypERcalcemia
Moans,
Stones,
Groans: GI cramping, diarrhea, etc.
Psychic overtones.
Differential dx of hypercalcemia.
Use pneumonic.
MISHAP
Malignancy (PThr & mets),
Idiopathic,
Sarcoid,
Hyperpara, hyperthyroid,
Addisons, vit A intox,
Pagets, Parathyroid hyperplasia.

All should have LOW PTh except hyperparathyroidism.
Workup of hyperparathyroidism?
Suspicion,
Blood work: Ca elevated, Cl:Ph >33 suggestive. Should "dump" CaCl.
Elevated PTh - diagnostic.
US, CT?
Surgery: single gland adenoma or 4 gland hyperplasia.
What should you do if in surgery you find a single gland enlargement (adenoma)?
(80%)
Remove enlarged gland.
What should you do if in surgery you find 4 gland hyperplasia?
MEN I
20% cases
Remove 3 1/2
or
Remove all 4 and re-implant 1/2 of one.
How does chronic renal failure PRE transplant cause hyperparathyroidism?
Pt holds onto phos and loses calc.
Low calc --> elevated PTh levels.
Normal compensation.
Causes 4 gland hyperplasia.
Surgery only if severe or if it's causing probs w/ phos, etc
How does chronic renal failure POST transplant cause hyperparathyroidism?
Parathyroid fails to reset and continues to hypersecrete.
High calcium now (because not losing via kidney) AND high PTh.
4 gland hyperplasia.
Do 3 1/2 gland removal.
Look at Adrenal Gland Vascular Anatomy and physical anatomy
Arterial supply from renal and phrenic arteries.
Adrenal arteries off of renal arteries.
L ven empties into L renal vein.
R vein empties into IVC directly!

Right adrenal looks bigger on CT because it is being squished down by the liver.
What hormones does the adrenal cortex secrete?
Outer layer: Aldosterone,
Middle: Cortisol,
Inner: Estrogen or Testosteron
What hormones does the adrenal medulla secrete?
Epinephrine, Norepi
Medical and surgical options for adrenal tumors?
Medical: suppress substance.

Surgical: remove tumor.
Symptoms of pheochromocytoma?
Sustained HTN or episodic HTN, tachycardia, headaches.

Vanillyl mandelic acid (VMA) and metanephrine in urine.

10% bilat.
What is a pheochromocytoma?
Tumor that secretes high amts of catecholamines, usually norepi, sometimes epi.

MEN II
Workup of pheochromocytoma?
CT to localize.

24 hr urine to look for VMA and metanephrine.
Treatment of pheochromocytoma?
Pre-op alpha THEN beta blockade.
Alpha blocker opens up vessels before giving beta blockers so w/ a lower BP, the blood can get through w/out resistence.
Remove tumor and adrenal gland.
ABCs of pheochromocytoma?
Alpha block and Agua (fluid).

Beta block.

Cut.
What is Conn's Syndrome?
Hyperaldosteronism from aldosterone producing adenoma.
High aldo from tumor, low renin from feedback loop.
Sustained HTN, hypernatremia and hypokalemia.
Workup and treatment of Conn's syndrome?
CT to localize tumor.

Excise gland/ adenoma.
What are the differences between Cushing's SYNDROME vs Disease 1 and Disease 2?
Syndrome: from exogenous steroids.

Disease 1*: pituitary adenoma causing increased ACTH causing increased cortisol.

Disease 2*: Lung Ca or adrenal tumor.
Signs/ symptoms of cushings syndrome and disease?
HTN,
Central obesity,
Stria,
DM,
Osteoporosis,
Hirsutism
What is the Dexamethasone Suppression Test?
A cortisol analog is given.
Normal pts will decrease cortisol production when challeneged w/ dexamethasone.
in pts w/ adrenal tumors, cortisol production remains high despite dexamethasone.
Give a low dose and high dose.
Treatment for Cushings?
Decrease exogenous steroids if that is the cause.
CT head AND abdomen.
Remove pit tumor or adrenal tumor or bilat adrenalectomy (in this case, need replacement therapy)
What is Addison's Disease?
Adrenal insufficiency, MC iatrogenic.
Also, autoimmune, TB, histoplasmosis, trauma, sepsis, surgery.
Presentation of Addisons?
Hypotension, low Na, high K, low gluc.

Usually cortisol part of gland is affected. If aldosterone, other things control BP, estrogen or testost affected, there are other places in the body that make these hormones and would prob go unnoticed. But if cortisol affected, no other place that makes cortisol and pt will be really sick.
Workup for Addisons?
Check gluc, lytes, and look at cortisol.
Look at these things if a pt has been acutely sick, should be getting better, but isn't.
They could be in adrenal crisis.
Treatment for Addisons?
Replace gluc and mineralcorticoids.

GIVE STEROIDS IF LIFE THREATENING!
What is an incidentaloma?
Adrenal mass found on CT.

If symptomatic, remove it after workup.
If asx, remove if >5 cm bc risk of cancer. If not, follow w/ serial CTs.
MEN: (Multiple Endocrine Neoplasia Syndromes) I:
3 ps
Pituitary Adenoma,
Parathyroid hyperplasia,
Pancreatic Islet Cell tumors (glucagonoma, insulinoma)
MEN IIa?
Parathyroid hyperplasia,
Medullary Ca,
Pheochromocytoma
Men IIb?
Medullary Ca,
Pheo,
Mucosal neuromas