U World questions 2 Flashcards
Pt states they have severe back pain for last 3 hours. Had intermittent back pain for last 3 wks. Has had trouble walking and urinating for last three weeks. Currently have increased DTRs and loss of sensation on LE. States pain is worse when lying down at night. PE pt’s vitals are WNL , point tenderness over T10.
Dx and Tx?
Dx: Spinal cord compression
Tx: IV glucocorticoids
*seen in pts with advanced prostate cancer
Pt presents and dx with TB. He has had wt loss, fatigue, fever and cough. Your attending states the TB has disseminated. What electrolyte abnormalities would you expect if it went to the adrenal gland?
Hyperkalemia, hyponatremia, hypoglycemia
See borderline hypotension as well.
*Adrenal insufficiency leads to decreased cortisol, sex hormones and aldosterone (Saves Sodium) and secretes potassium and H ions. Low aldo–> Na loss, retain K and H+ === normal anion gap metabolic acidosis
Conditions leading to elevated anion gap
Ketoacidosis (alcohol, starvation, diabetic), intoxicatin ( methanol, salicylate, ethylene glycol, isoniazide, metformin), tissue hypoxia (ischemia, CO or CN poison_ and renal fail or uremia
Excessive vomitting, hyperaldo and excessive volume contraction (thiazide or loops) lead to the acid base disturbance
Metabolic alkalosis
What leads to respiratory acidosis?
Conditions causing improper ventilation
What conditions cause hyperventilation?
What acid/base disturbance results?
Pulmonary parenchymal disease–> respiratory fail. you see tachypnea and dyspnea
Causes respiratory alkalosis
Vit deficiency/toxicity: angular cheilosis, stomatitis, glossitis with normocytic anemia and seborheic dermatitits
Riboflavin or B2 deficiency
Vit deficiency/toxicity causes cheilosis, stomatitis and glossitis with irritability, confusion and depression?
Pyridoxine or B6
Patient comes in with cold intolerance, wt gain, oligomenorrhea. Labs show low T4 and elevated TSH with +TPO antibodies. What cancer is she at increased risk for?
Hashimoto thyroiditis
60 times higher chance of developing thyroid lymphoma
What is the classic triad seen in renal cell carcinoma?
What are other signs of RCC?
What test do you order to dx?
flank pain, hematuria, palpable abdominal mass
*hematuria= tumor in collecting system
Scrotal varicoceles that fail to empty is sign
*may have ectopic production of EPO–> polycythemia
Test: get Abdominal CT!!!
PSVT is the most common paroxysmal tachycardia in people w/out structual heart dx. Attacks start abruptly–> HR btwn 160-220 with palpitations. OFten d/t re-entry into AV node. What can people do to end the attacks?
Vagal maneuvers: valsalva, carotid sinus massage or immersion in cold water
Works by increasing vagal tone and decreasing conduction through AV node.
Otherwise use Adenosine; short acting AV node blocker
Pt comes in and you suspect acromegaly. What test do you order first?
If that test is abnormal, what is the next step?
And the last step?
- IGF-1 level; if ELEVATED then get next test
- Oral glucose suppression test; if adequte GH suppression order it’s NOT acromegaly.
Inadequate suppresion–> next test - MRI of brain; may see pituitary mass
If NO mass eval for extra-pit causes of acromegaly
Pt comes in with left arm weakness… several months ago she experienced vertigo that went away after a few weeks. On PE she is asked to close her eyes and stretch her arms out with palms up. Seconds later the left arm drifts down with palm facing the floor. Why? Where is the lesion?
Pyramidal tract disease (Pronator drift is very specific for Upper motor neuron dx)
Pt likely has MS ( neurodeficiets disseminated in space and time)
What happens to cortisol, ACTH and Aldosterone in Chronic glucocorticoid therapy (Central Adrenal insufficiency)?
Decrease Cortisol
Decrease ACTH
normal Aldosterone (however, may see low Na d/t elevated ADH)
What happens to cortisol, ACTH and Aldosterone in Primary Adrenal insufficiency?
all will be DECREASED
see hyperpigmentation, hyperK, hypoNa, hypotension
What is the inheritance pattern for myotonic dystrophy?
What about for Becker dystrophy?
Duchenne?
Myotonic is Auto.Dominant (CTG repeat); onset 12-30 yo w /facial weakness, hand grip myotonia and dysphagia. see cataracts, balding, testicular atrophy
Becker: X-link Recessive del of dystrophin; less severe–onset age 5-15 with death at 40-50 HF
Duchenne: Xlink Recessive; del of dystrophin; onset 2-3 w/ Gower sign death from heart or respiratory fail
Common findings of PE:
Less common findings of PE:
RF of PE
Dyspnea, tachypnea, tachycardia
less common: hemoptysis from peripheral pulm artery by thrombus–> pulmonary infarct. lead to pleuritic chest pain
RF: immobilizatin, hx PE,
When do you see elevated oligoclonal bands in CSF?
In MS!
Condition in new moms holding their babies with thumb outstretched; abducted and extended; abductor pollicis longus and extensor pollicus longus are affected
De Quervain tenosynovitis
Tx of choice for pregnant or lactating women or children under the age of 6 with Lyme’s disease?
Tx w/ Amoxicillin (doxycycline contraindicated in preggers d/t teeth staining)
What is the gold standard to dx Duchenne muscular dystrophy?
Genetic Testing; XLR
Patient presents with BP of 97/50, distant heart sounds and JVD. Likely dx
cardiac tamponade
Mg is excreated by the ____
kidneys!
if elevated creatinine in patient, may need less Mg then expected or can lead to Mg toxicity
Tx: calcium gluconate
What meds can you give pt suffering from migraine + nausea and photophobia?
IV antiemetics; chlorpromazine, prochlorperazine or metoclopramide
*amitriptyline better for prophylaxsis
Recurrent infections in little kids. Have low platelets and dry, scaly skin. Likely dx?
Cause?
Tx?
Dx: Wiskott- Aldrich syndrome
Cause: X linked recessive defect in WAS gene–> issue w/ hematopoetic cells and cytoskeleton dysfnx
Tx: hematopoietic stem cell transplant
What are the Sx of Waldenstroms macroglobulinemia?
how do you dx it?
Sx: hepatospelnomegaly and enlarged LN, night sweats, peripheral neuropathy, anemia, headach and dizzy with vision problems
Issue with terminally dif B cells –> spike in IgM and hyperviscocity of blood!
What do the immunoglobulins look like in multplile myeloma?
Either elevated IgA or IgG
Hemolysis leading to hemoglobinuria
Cytopenias leading to fatigue and dyspnea
Hypercoaguable state–acute abdominal pain form severe hemolysis or portal vein thrombosis
usually apreas by 4th decade. Pt have ELEVATED bilirubin and LDH with LOW haptoblobin
Dx and mechanism?
Paroxsymal nocturnal hemoglobinuria
autoimmune hemolytic dx w/ intra and extravascular hemolysis. Genetic defecct of cell surface anchor making them vulnerable to MAC and complement