Endocrine, Head & Neck Flashcards

1
Q

Management of septal hematoma

A

Early I&D (otherwise there can be fibrosis and necrosis of septal cartilage)

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2
Q

Cushing disease

A

ACTH-secreting pituitary adenoma

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3
Q

Diagnosis of gastrinoma

A

Serum gastrin >1000 or
Paradoxical increase in gastrin with secretin administration

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4
Q

Symptoms of glucagonoma

A

Anemia, diabetes, stomatitis, dermatitis, weight loss

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5
Q

Diagnosis of glucagonoma

A

Fasting serum glucagon >500-1000

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6
Q

Insulinoma symptoms

A

Anxiety, dizziness, confusion, personality changes, seizures (sx worse in the morning)

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7
Q

Diagnosis of insulinoma

A

72hr observed fast

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8
Q

Location of insulinoma

A

Evenly distributed throughout pancreas

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9
Q

Somatostatinoma symptoms

A

Steatorrhea, diabetes, hypochlorhydria, cholelithiasis

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10
Q

Somatostatinoma diagnosis

A

Fasting plasma somatostatin >100

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11
Q

VIPoma diagnosis

A

Serum VIP level 250-500

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12
Q

What cancers are Peutz-Jeghers at risk for

A

Pancreatic, breast

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13
Q

S-100 tumor marker - associated with?

A

Melanoma, neurofibroma, schwannoma

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14
Q

Vimentin tumor marker - associated with?

A

Melanoma, colon, esophageal, gastric

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15
Q

KRAS tumor marker - associated with?

A

Melanoma, colon

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16
Q

HER2 tumor marker - associated with?

A

Breast, ovarian, lung, gastric, oral cancers

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17
Q

Management incidentaloma - when to resect?

A

When >6cm (consider if 4-6cm)

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18
Q

Chemoprevention for patients with FAP after TAC + ileorectal anastomosis

A

Sulindac

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19
Q

VHL screening for which cancers

A

CNS and retinal hemangioblastomas, RCC, and pheochromocytomas

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20
Q

Most common location for undifferentiated spindle cell tumor

A

Proximal tibia and distal metaphysis of femur

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21
Q

Histology of undifferentiated spindle cell tumor

A

Fibroblasts in whirling patterns with multinucleated giant cells, inflammatory cells, and foamy mononuclear giant cells

22
Q

Management of spindle cell tumors

A

Neoadjuvant chemo -> surgery with wide margins

23
Q

Histology of pleomorphic adenoma (salivary gland tumor)

A

Stromal tissue with groups of epithelial and myoepithelial cells

24
Q

Most common mutation in PDAC

25
Only thyroid cancer that metastasizes hematogenously
Follicular
26
Management of follicular thyroid cancer
Partial thyroidectomy Total thyroidectomy only done if: radioactive iodine therapy is planned, nodule is >4cm, extrathyroidal invasion, or mets
27
Pathology of papillary thyroid cancer
Intranuclear inclusion bodies (Orphan annie eyes), Psammoma bodies
28
Follow-up for medullary thyroid cancer after resection
CEA & calcitonin q3-6mo [Neck US if any suspicion of recurrence]
29
MEN1 syndrome
Pituitary adenomas Hyperparathyroidism PNETs
30
MEN2A
Medullary thyroid cancer Hyperparathyroidism Pheochromocytoma
31
MEN2B
Medullary thyroid cancer Pheochromocytoma Mucosal neuromas Marfanoid habitus
32
MEN4 syndrome
Hyperparathyroidism Pituitary tumors Neuroendocrine tumors Uterine, testicular, colonic tumors
33
Gene mutation in MEN4 syndrome
CDKN1B
34
Maxillary torus
Benign osteoblastic tumor arising from the hard palate
35
What to give if hypertensive episode occurs intraop with pheochromocytoma
Nicardipine or nitroprusside (titratable agents)
36
What if you get Hurthle cells on thyroid FNA?
Non-diagnostic -> patient should get a diagnostic thyroid lobectomy
37
Gastrinoma triangle borders
CBD, neck of pancreas, and 3rd portion of duodenum
38
Most common location of an ectopic superior parathyroid gland
Tracheoesophageal groove
39
Boundaries of a central neck dissection
Hyoid bone (superior) Innominate artery (inferior) Carotid arteries (lateral)
40
Most common location for Ewing sarcoma
Pelvis (onion skin appearance)
41
What is the hypothesized reason for resistance to radiation therapy?
Tumor hypoxia and low levels of oxygen free radicals
42
When to FNA a thyroid nodule
>1cm Hypoechoic Solid Irregular margins Any calcifications Taller-than-wider shape
43
Bethesda criteria for thyroid cytopathology: I
Nondiagnostic Repeat FNA in 4-6wks
44
Bethesda criteria for thyroid cytopathology: II
Benign Observation with repeat US in 1-2yrs
45
Bethesda criteria for thyroid cytopathology: III
Atypia/follicular lesion of unknown significance Molecular testing or surgery
46
Bethesda criteria for thyroid cytopathology: IV
Follicular neoplasm Molecular testing or surgery
47
Bethesda criteria for thyroid cytopathology: V
Suspicious for malignancy Surgery
48
Bethesda criteria for thyroid cytopathology: VI
Malignant Surgery
49
Calcium-to-creatinine clearance ratio >0.02 with hypercalcemia
Primary hyperparathyroidism
50
Calcium-to-creatinine clearance ratio <0.01 with hypercalcemia
FHH
51
Monitoring for nonfunctioning adrenal tumor
Imaging in 6, 12, and 24 mo Annual hormone testing for 4yrs (If growth more than 1cm/yr or hormonal secretion: resect)