Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
142 Cards in this Set
- Front
- Back
MEN 1
|
Pituitary, pancreas, parathyroid
|
|
MEN 2A
|
Pheo, parathyroid, medullary thyroid
|
|
MEN 2B
|
Pheo, medullary thyroid, marfanoid, mucocutaneous neurofibromas
|
|
The recurrent laryngeal nerve innervates all laryngeal muscles except ____
|
Cricothyroid (sup. laryngeal n.)
|
|
Thyroid follicles store enough T4 to last ____
|
2-3 months
|
|
Tx: Graves’
|
Meds, radioiodide ablation
|
|
Dx: tachycardia, diarrhea, lower extremity edema, weight loss, amenorrhea
|
Hyperthyroid
|
|
Management of thyroid storm
|
Beta blockers, antithyroid meds, corticosteroids, sodium iodide
|
|
Effect of glucocorticoids on thyroid homeostasis
|
Block peripheral T4 conversion
|
|
Dx: fatigue, low mood, constipation, neck pain, menorrhagia
|
Subacute thyroiditis
|
|
Define: Riedel’s thyroiditis
|
Fibrous replacement of thyroid
|
|
Which nodules are likely benign, hot or cold?
|
Hot
|
|
__% of thyroid nodule FNAs will show a benign lesion
|
65%
|
|
MC presentation of thyroid cancer
|
Painless mass
|
|
Possible associated symptoms of thyroid cancer
|
Dysphonia, hoarseness, dysphagia, dyspnea
|
|
Amyloid on thyroid FNA is diagnostic of ____ cancer
|
Medullary cancer
|
|
Parathyroid embryology
|
3rd pouch: Inferior glands; 4th pouch: superior glands
|
|
The only thyroid cancer that undergoes hematogenous metastases
|
Follicular
|
|
Principal parathyroid cell
|
Chief cell
|
|
Tx: acute hypercalcemia
|
Aggressive IVF, Lasix, and bisphosphonates
|
|
GI sx of hypercalcemia
|
Nausea, vomiting, constipation, PUD, pancreatitis
|
|
Rare electrolyte cause of hypoparathyroidism
|
Chronic hypomagnesemia
|
|
Adrenal arterial supply
|
Aorta, inferior phrenic, and renal arteries
|
|
Adrenal venous drainage
|
Right drains to IVC, left drains to L renal vein
|
|
¾ of the mass of the adrenals comes from the ___ layer
|
Fasciculata
|
|
Categorization of adrenal masses by size
|
<6 = observe, >6 resect
|
|
MC paraneoplastic syndrome associated with adrenocortical carcinoma
|
Cushings
|
|
Define: Nelson’s syndrome
|
Post-adrenalectomy pituitary hyperplasia: hypersecretion of ACTH, mass lesion, hyperpigmentation, amenorrhea
|
|
Dx: weight gain, loss of muscle mass, bruising, acne, fatigue
|
Cushing’s
|
|
Suppression with high-dose dexamethasone confirms cortisol of ____ origin
|
Adrenal or ectopic
|
|
Classic symptoms of Addisonian crisis
|
Abdominal pain, altered mental status
|
|
Sx of Addison’s
|
Fatigue, nausea, vomiting, abdominal pain, weight loss, hyperpigmentation
|
|
Dx: diastolic hypertension without edema
|
Primary hyperaldosteronism
|
|
Blueberry muffin sign
|
Subcutaneous blue tumor nodules in neuroblastoma
|
|
MC extraadrenal site for pheochromocytoma
|
Organ of Zuckerkandl (level of aortic bifurcation)
|
|
Intraoperative management of pheochromocytoma
|
Alpha blockade FIRST, and then beta blockade
|
|
Size classification: pituitary micro- vs. macroadenoma
|
<1 cm: micro-; >1cm macro-
|
|
Two MC indications for splenectomy
|
Trauma and ITP
|
|
Conditions associated with splenic rupture
|
EBV, malaria, trauma, abscess
|
|
Breast arterial supply
|
Internal mammary, axillary, and intercostals
|
|
The majority of venous drainage of the breast is accomplished by the ___ vein
|
Axillary
|
|
The smallest breast mass detectable by physical exam is ___
|
1 cm
|
|
Damage to the medial and/or lateral pectoral nerves during axillary node dissection will leading to what deficit?
|
Pectoral weakness.
|
|
Damage to the thoracodorsal nerve during axillary node dissection will leading to what deficit?
|
Latissimus weakness
|
|
Damage to the long thoracic nerve during axillary node dissection will leading to what deficit?
|
Scapula winging
|
|
Evaluation of a breast mass in most women
|
Diagnostic mammography +/- US +/- FNA
|
|
Evaluation of a breast mass in young women under 30
|
US +/- FNA
|
|
Define: hidradenitis suppurativa
|
Chronic infection of apocrine sweat glands, often manifesting on the areola in women
|
|
Classic benign breast lesion that feels just like cancer
|
Fat necrosis
|
|
Diagnostic evaluation of suspected fibroadenoma
|
FNA
|
|
Define: Mondor’s disease
|
Superficial thrombophlebitis of lateral thoracic veins
|
|
Presentation of Mondor’s disease
|
Acute axillary/lateral breast pain with a palpable tender cord
|
|
Natural history of Mondor’s disease
|
Self-limiting over the course of several weeks with NSAIDs
|
|
Typical cause of Mondor’s disease
|
Local trauma or surgery
|
|
Most likely diagnosis: 35-year-old woman with bilateral, nodular breast tenderness and straw-colored nipple discharge that is worst during menses
|
Fibrocystic change
|
|
Dx: non-cyclic breast pain with lumps under the areolar-nipple complex
|
Ductal ectasia
|
|
MCC of bloody nipple discharge
|
Intraductal papilloma
|
|
Which breast process is clinically indistinguishable from fibroadenoma but tends to happen in old rather than young women?
|
Phyllodes tumor (smooth, well-marginated, mobile, painless)
|
|
Dx: tender, itchy nipple with bloody discharge
|
Paget’s disease of the breast
|
|
Three genetic conditions associated with breast cancer
|
Li Fraumeni, BRCA, Peutz-Jeghers
|
|
Contraindications to breast lumpectomy
|
Previous radiation, multicentric disease, and connective tissue diseases
|
|
Initial lab work for burn patients
|
ABG, CBC, electrolytes, carboxyhemoglobin
|
|
Rule of 9s for burns
|
9% each arm, 9% head, 18% chest, 18% back, 18% each leg, 1% perineum
|
|
Parkland formula for adult burns
|
4 mL/kg/% body surface area burned; five first half over 8 hours, give second half over 16
|
|
When is resuscitation adequate in burn management?
|
UOP > .5 cc/kg/hr in adults, 1 in kids
|
|
MC complication of inhalational injury
|
Pneumonia
|
|
Key management point for victims of electrical burns
|
Continuous cardiac monitoring
|
|
What kind of injury does alkaline material cause?
|
Liquefactive necrosis
|
|
What kind of injury does acidic material cause?
|
Coagulative necrosis
|
|
Define: Marjolin’s ulcer
|
“Burn cancer”; aggressive squamous cell carcinoma with nodal mets
|
|
Define: coronary artery “dominance”
|
Which coronary artery gives rise to the posterior descending artery (90% of the time, the RCA)
|
|
Flow through a vessel is significantly impedes when atherosclerotic plaque occupies >__% of the cross sectional area of the lumen
|
75%
|
|
Two groups of patients who have “atypical” MI symptoms
|
Women, diabetics, and the elderly
|
|
Conduits used for CABG
|
Internal mammary artery, radial artery, inferior epigastric artery, saphenous vein,
|
|
Generalized CABG indications by degree of coronary stenosis
|
Left main > 60% stenosis, or proximal LAD and circ >70% stenosis.
|
|
MCC of mitral stenosis
|
Rheumatic heart disease
|
|
Dx: mid-diastolic murmur with opening snap
|
Mitral stenosis
|
|
How can ischemic heart disease cause mitral insufficiency?
|
Papillary muscle dysfunction
|
|
MCC of mitral insufficiency
|
Mitral valve prolapse (myxomatous degeneration)
|
|
Dx: holosystolic murmur radiating to the axilla
|
Mitral insufficiency
|
|
Principles of medical management for mitral insufficiency
|
Reduce afterload (lower BP) to reduce the volume of regurgitant blood
|
|
MCC of aortic stenosis
|
Calcific changes to native or bicuspid valve
|
|
MCC of aortic insufficiency
|
Aortic root dilation, endocarditis
|
|
Dx: decrescendo diastolic murmur on the R
|
Aortic insufficinency
|
|
Which worsens with inspiration, tricuspid or mitral stenosis?
|
Tricuspid stenosis
|
|
Most small cell lung cancers are ___ located, whereas most non-small cell lung cancers are ___ located
|
Centrally; peripherally
|
|
Small cell lung cancers are treated with ___, while non-small cell cancers are treated with ___.
|
Chemotherapy, surgery.
|
|
Small cell lung cancer paraneoplastic syndromes
|
Cushings, SIADH
|
|
Squamous lung cancer paraneoplastic syndrome
|
Hypercalcemia PTH-rP
|
|
Dx: acute, stabbing chest pain and neurologic signs
|
Thoracic aortic dissection involving one or more head/neck vessels
|
|
Acute medical management of thoracic aortic dissections
|
Labetalol, nitroprusside
|
|
Blood supply to penis
|
Internal pudendal artery
|
|
How does management of a torsed appendix epididymis differ from that of a torsed testicle?
|
Appendix epididymis is managed with NSAIDs, self-limited.
|
|
What muscle do the ureters lie upon?
|
Psoas
|
|
What is the anatomic landmark for where the ureters cross the iliacs?
|
Anterior to iliac bifurcation
|
|
Normal red cells per high powered field in urine
|
<3
|
|
Classic drug associated with priapism
|
Trazadone
|
|
Classic sign of epididymitis in patient with acute scrotum
|
Relief of pain with elevation of affected testis
|
|
Classic physical exam for testicular torsion
|
High-riding testicle with transverse lie and loss of cremasteric reflex
|
|
Most patients with torsion are ___; the opposite is true of patients with epididymitis
|
Afebrile
|
|
__ kidney stones are note visible of plain film
|
Urate
|
|
Most kidney stones less than ___ in size will pass spontaneously
|
< 5 mm
|
|
Places where a kidney stone might get stuck
|
Ureteropelvic junction, pelvic brim, iliac crossing, ureterovesical junction, vesical origin
|
|
Medical management of BPH
|
5α reductase inhibitors; α antagonists
|
|
Risk factors: RCC
|
Smoking
|
|
Possible paraneoplastic hormones of RCC
|
PTH-rP; ACTH; Prolactin; EPO
|
|
MC location for branchial cleft cyst
|
Anterior border of sternocleidomastoid
|
|
Define: cystic hygroma
|
Congenital lymphangioma
|
|
MC location for cystic hygroma
|
Oropharyngeal, particularly floor of the mouth
|
|
MC tracheoesophageal malformation
|
Blind esophageal pouch with distal TE fistula
|
|
Dx: baby with excessive drooling and no gastric air bubble
|
TE fistula
|
|
VACTERL association
|
Vertebral/anal/cardiac/TE fistula/renal/limb
|
|
MC form of congenital diaphragmatic hernia
|
Bochdalek (posterolateral)
|
|
Define: Morgagni hernia
|
Retrosternal congenital diaphragmatic hernia
|
|
Dx: neonate with respiratory distress and scaphoid abdomen
|
Congenital diaphragmatic hernia
|
|
Define: “pulmonary sequestration”
|
Nonfunctional cystic pulmonary unit that does not communicate with airways and directly receives its blood supply from the aorta
|
|
Classic CXR for pulmonary sequestration
|
Child with pulmonary mass lesion and air-fluid level
|
|
Define: “Congenital Cystic Adenomatoid Malformation”
|
Abnormal development of pulmonary tissue, replaced by nonfunctional cystic mass; often an entire lobe
|
|
Presentation of Congenital Cystic Adenomatoid Malformation
|
RDS or recurrent pulmonary infections
|
|
On CXR, congenital cystic adenomatoid malformation is often mistaken for ___
|
Congenital diaphragmatic hernia
|
|
How can you tell the difference between CCAM and congenital diaphragmatic hernia on CXR?
|
NG tube placement
|
|
Define: gastroschisis
|
Open midline herniation of abdominal contents
|
|
Common complication of gastroschisis
|
NEC
|
|
Define: omphalocele
|
Herniation of abdominal contents into umbilical sac
|
|
In addition to bowel, omphalocele often classically involves which organ?
|
Liver
|
|
Associated conditions: omphalocele
|
Beckwith-Wiedemann; trisomies 13 and 18
|
|
Define: “Littre’s hernia”
|
Hernia containing a Meckel’s diverticulum
|
|
MC hernia in children
|
Indirect inguinal 2/2 patent processus vaginalis
|
|
Inguinal hernias in kids are more common on the __ side
|
R side
|
|
Dx: baby with very acute onset bilious vomiting and distention
|
Malrotation with midgut volvulus
|
|
Dx: baby with chronic bilious vomiting and distention
|
Duodenal atresia
|
|
The “double bubble sign” is present in which two conditions?
|
Midgut volvulus and duodenal atresia
|
|
Classic triad: intussusception
|
Intermittent abdominal pain, bilious vomiting, currant jelly stools
|
|
Classic appendicitis mimic in kids
|
Meckel’s diverticulum
|
|
Dx gold standard for Meckel’s diverticulum
|
Scintigraphy: sensitive to ectopic gastric mucosa
|
|
MCC of lower GI obstruction in neonates
|
Hisrchsprung’s
|
|
MC presentation of Hirschsprung’s disease
|
Delayed passage of meconium
|
|
Dx: neonate with fever, lethargy, distention, hematochezia
|
NEC
|
|
MC intraabdominal malignancy in childhood
|
Wilm’s tumor
|
|
MC non-CNS solid tumor of childhood
|
Neuroblastoma
|
|
Wilm’s tumor triad
|
Flank pain, hematuria, HTN in a child
|
|
Presentation of neuroblastoma
|
Abdominal pain, constitutional symptoms, neurologic signs, HTN
|