Endocrine, Head & Neck Flashcards
Management of septal hematoma
Early I&D (otherwise there can be fibrosis and necrosis of septal cartilage)
Cushing disease
ACTH-secreting pituitary adenoma
Diagnosis of gastrinoma
Serum gastrin >1000 or
Paradoxical increase in gastrin with secretin administration
Symptoms of glucagonoma
Anemia, diabetes, stomatitis, dermatitis, weight loss
Diagnosis of glucagonoma
Fasting serum glucagon >500-1000
Insulinoma symptoms
Anxiety, dizziness, confusion, personality changes, seizures (sx worse in the morning)
Diagnosis of insulinoma
72hr observed fast
Location of insulinoma
Evenly distributed throughout pancreas
Somatostatinoma symptoms
Steatorrhea, diabetes, hypochlorhydria, cholelithiasis
Somatostatinoma diagnosis
Fasting plasma somatostatin >100
VIPoma diagnosis
Serum VIP level 250-500
What cancers are Peutz-Jeghers at risk for
Pancreatic, breast
S-100 tumor marker - associated with?
Melanoma, neurofibroma, schwannoma
Vimentin tumor marker - associated with?
Melanoma, colon, esophageal, gastric
KRAS tumor marker - associated with?
Melanoma, colon
HER2 tumor marker - associated with?
Breast, ovarian, lung, gastric, oral cancers
Management incidentaloma - when to resect?
When >6cm (consider if 4-6cm)
Chemoprevention for patients with FAP after TAC + ileorectal anastomosis
Sulindac
VHL screening for which cancers
CNS and retinal hemangioblastomas, RCC, and pheochromocytomas
Most common location for undifferentiated spindle cell tumor
Proximal tibia and distal metaphysis of femur
Histology of undifferentiated spindle cell tumor
Fibroblasts in whirling patterns with multinucleated giant cells, inflammatory cells, and foamy mononuclear giant cells
Management of spindle cell tumors
Neoadjuvant chemo -> surgery with wide margins
Histology of pleomorphic adenoma (salivary gland tumor)
Stromal tissue with groups of epithelial and myoepithelial cells
Most common mutation in PDAC
KRAS
Only thyroid cancer that metastasizes hematogenously
Follicular
Management of follicular thyroid cancer
Partial thyroidectomy
Total thyroidectomy only done if: radioactive iodine therapy is planned, nodule is >4cm, extrathyroidal invasion, or mets
Pathology of papillary thyroid cancer
Intranuclear inclusion bodies (Orphan annie eyes), Psammoma bodies
Follow-up for medullary thyroid cancer after resection
CEA & calcitonin q3-6mo
[Neck US if any suspicion of recurrence]
MEN1 syndrome
Pituitary adenomas
Hyperparathyroidism
PNETs
MEN2A
Medullary thyroid cancer
Hyperparathyroidism
Pheochromocytoma
MEN2B
Medullary thyroid cancer
Pheochromocytoma
Mucosal neuromas
Marfanoid habitus
MEN4 syndrome
Hyperparathyroidism
Pituitary tumors
Neuroendocrine tumors
Uterine, testicular, colonic tumors
Gene mutation in MEN4 syndrome
CDKN1B
Maxillary torus
Benign osteoblastic tumor arising from the hard palate
What to give if hypertensive episode occurs intraop with pheochromocytoma
Nicardipine or nitroprusside (titratable agents)
What if you get Hurthle cells on thyroid FNA?
Non-diagnostic -> patient should get a diagnostic thyroid lobectomy
Gastrinoma triangle borders
CBD, neck of pancreas, and 3rd portion of duodenum
Most common location of an ectopic superior parathyroid gland
Tracheoesophageal groove
Boundaries of a central neck dissection
Hyoid bone (superior)
Innominate artery (inferior)
Carotid arteries (lateral)
Most common location for Ewing sarcoma
Pelvis (onion skin appearance)
What is the hypothesized reason for resistance to radiation therapy?
Tumor hypoxia and low levels of oxygen free radicals
When to FNA a thyroid nodule
> 1cm
Hypoechoic
Solid
Irregular margins
Any calcifications
Taller-than-wider shape
Bethesda criteria for thyroid cytopathology: I
Nondiagnostic
Repeat FNA in 4-6wks
Bethesda criteria for thyroid cytopathology: II
Benign
Observation with repeat US in 1-2yrs
Bethesda criteria for thyroid cytopathology: III
Atypia/follicular lesion of unknown significance
Molecular testing or surgery
Bethesda criteria for thyroid cytopathology: IV
Follicular neoplasm
Molecular testing or surgery
Bethesda criteria for thyroid cytopathology: V
Suspicious for malignancy
Surgery
Bethesda criteria for thyroid cytopathology: VI
Malignant
Surgery
Calcium-to-creatinine clearance ratio >0.02 with hypercalcemia
Primary hyperparathyroidism
Calcium-to-creatinine clearance ratio <0.01 with hypercalcemia
FHH
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)