Endocrine Disorders Flashcards

(54 cards)

0
Q

Hx of neck radiation w/ nodule –> next step?

A

Appropriate to move straight to thyroidectomy

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1
Q

Important factors in H&P of thyroid nodule?

A

Radiation hx, family hx, voice and airway, sx, thyroid nodule pattern

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2
Q

Which type of thyroid cancer is inherited? Dx?

A

Medullary (MEN syndromes - RET gene - AD trait)

Calcitonin levels

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3
Q

Signs/sx concerning for thyroid malignancy?

A

Hoarseness, hard/fixed nodule, dyspnea, dysphagia, cervical LN enlargement, vocal cord paralysis

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4
Q

Risk of solitary nodule vs dominant nodule in multinodular gland

A

15% vs 5%

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5
Q

T/F: radioactive iodine scanning is appropriate initial eval of solitary thyroid nodule

A

F

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6
Q

Usefulness of US in thyroid eval?

A

Distinguishing cyst from nodules, following the size or recurrence of cysts following FNA

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7
Q

FNA shows psammoma bodies?

A

Papillary cancer

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8
Q

FNA shows amyloid deposits

A

Medullary cancer

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9
Q

FNA shows Hurthle cells? Tx

A

Adenoma or low-grade cancer –> lobectomy, total thyroidectomy

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10
Q

FNA shows lymphocytic infiltrate? Dx, Tx

A

Lymphoma or chronic lymphocytic thyroiditis

Flow cytometry

Radiosensitive –> radiation appropriate

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11
Q

Risks of thyroid surgery?

A

Recurrent laryngeal nerve injury, ex branch of superior laryngeal nerve injury (alters high-pitch singing), parathyroid

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12
Q

MC type of thyroid cancer?

A

Papillary

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13
Q

Papillary cancer w/ prior head/neck radiation

A

Total thyroidectomy

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14
Q

Papillary cancer w/ no hx of radiation

A

lobectomy and isthmusectomy

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15
Q

thyroid cancer more prevalent in iodine-deficient areas?

A

Follicular

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16
Q

Follicular < 4 cm and > 4 cm (microinvasive)

Clear follicular cell carcinoma

A

Lobectomy/isthmusectomy vs total thyroidectomy

total thyroidectomy > 1 cm

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17
Q

Route of spread of follicular cancer?

A

Vascular

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18
Q

Medullary cancer cell type?

A

C cell hyperplasia (parafollicular cells) w/ amyloid

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19
Q

Papillary carcinoma prognosis

A

High survival in well-differentiated (100% at 10 years) and low in high-risk pts (20%)

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20
Q

Post-op management of papillary cancer

A

thyroid suppression w/ TH and maybe Iodine ablation

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21
Q

Follicular cancer prognosis and post-op tx

A

80% v 60%

Iodine ablation

22
Q

Medullary prognosis and post-op tx

A

80% vs 45%

NOT iodine/TH (wrong cells) –> CEA and calcitonin

23
Q

Most common met site of anaplastic thyroid cancer?

24
Hyperparathyroid localization?
Sestamibi scan
25
MC location for missing inferior parathyroid gland?
Thymus
26
Chvostek's sign
tapping facial nerve near the ear results in spasm of orbicularis oris (hypocalcemia)
27
Common malignant cause of hypercalcemia?
Metastatic carcinoma (breast), multiple myeloma, sarcoidosis, vitamin A intoxication, thiazides, renal cell carcinoma, SqCC of lung (PTHrP), familial hypocaliuric hypercalcemia
28
Acute tx of hypercalcemia?
Results in an osmotic diuresis --> dehydration 1. rehydrate w/ NS 2. Lasix 3. bisphosphonates 4. mithramycin, calcitonin, glucocorticoids
29
Surgical indications in Secondary Hyperparathyroidism
Bone pain, fx, intractable pruritis, ectopic calcifications in soft tissues (calcium tachyphylaxis)
30
Hyperparathyroidism and HTN in same pt? Tx?
Possible pheochromocytoma. Combo alpha/beta blocker (never beta alone as unopposed alpha stimulation can be fatal)
31
Test for Pheochromocytoma?
10% tumor; 10% malignant, extra-adrenal, epinephrine producers, and bilateral --> MRI T2 weighted, octreotide scan, MIBG scan (last resort) selects for chromaffin tissue
32
Pheochromocytoma tx?
Alpha blockade - Phenoxybenzamine (10-14 days) prior to surgery Beta blockade Resection
33
Resection of pheochromocytoma? Important step?
Resect w/ MINIMAL manipulation to avoid catecholamine surge. Ligate all venous drainage before manipulation
34
Acute tender neck mass
Painful thyroiditis --> de Quervain's thyroiditis
35
de Quervain's course?
Early = hyperthyroidism due to acutely injured follicles releasing TH
36
de Quervain's histology?
Giant cell granulomas
37
de Quervain's tx?
Analgesics, aspirin, steroids
38
Is surgery appropriate in some cases of acute thyroid inflammation?
Bacterial infection (acute suppurative thyroiditis); Strep, Staph, Pseudomonas --> drainage
39
PAINLESS thyroid mass w/ hypothyroidism
Hashimoto's (chronic lymphocytic thyroiditis)
40
Management of Hashimoto's: Labs? Tx?
T3/T4, TSH ; Thyroid replacement, bx
41
Higher incidence of malignancy w/ Hashimoto's or de Quervain's
Hashimoto's (papillary, lymphoma)
42
Hx of hyperparathyroidism (3 gland resection) and intractable duodenal ulcers. Next steps?
1. r/o H. pylori | 2. Serum gastrin level (> 600 suspect Zollinger-Ellison, > 1000 dxic)
43
Sx of gastrinoma; Dx? Anatomy?
PUD, Diarrhea, esophagitis ; Serum gastrin, Secretin stimulation test ; Duodenum and head of pancreas (gastrinoma triangle)
44
Two types of ZE?
Sporadic, familial (MEN-1)
45
Pituitary sx from MEN-1?
Vision changes (local compression), hypersecretion (lactation)
46
Surgery for gastrinoma?
Yes. Endoscopy to localize, US to isolate --> surgical enucleation or Whipple depending on location
47
Medical management of gastrinoma?
Streptozocin.
48
What is the Whipple triad?
fasting hypoglycemia (< 60), sx hypoglycemia, relief by admin of glucose --> elevated insulin secretion (C peptide measurement)
49
MEN-2a
Medullary thyroid cancer, parathyroid hyperplasia, pheochromocytoma
50
MEN-2b
Similar to MEN-2a w/ exception of associated MARFANoid habitus and ganglioneuromas
51
Incidental adrenal mass: size suspicious of cancer?
> 5 cm
52
Adrenal carcinoma: where might it be a met from?
Lung cancer, others (adrenals common met location)
53
Incidental adrenal mass workup?
Catecholamines, Cortisol, Potassium --> if functional mass = removal Nonfunctional --> serial CT observation