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103 Cards in this Set

  • Front
  • Back
what immunosuppresant matches the following:

Derivative of 6-MP:
Nephrotoxic in 75% of pts:
Inhibits dihydrofolate reductase:
Derivative of 6-MP: Azathropine
Nephrotoxic in 75% of pts: Cyclosporine (prevent with mannitol)
Inhibits dihydrofolate reductase: MTX
what enzyme is deficient in the following dz's?

Fructose intolerance:
essential fructosuria:
classic galactosemia:
Fructose intolerance: aldolase B
essential fructosuria: fructokinase
classic galactosemia: galactose-1-phosphate uridyltransferase
what might you see in a first trimester ultrasound of a fetus with Downs
increased nucal translucency
which protozoa fits the following:

Ixodes tick is the vector:
Sodium stibogluconate is the tx:
Maltese cross seen in RBC:
severe diarrhea in AIDS:
Ixodes tick is the vector: bebesia
Sodium stibogluconate is the tx: Leschmania
Maltese cross seen in RBC: Babesia
severe diarrhea in AIDS: cryptosporidium

note: babesia is often a co-infection of Lyme and gives malaria like sx
what is the result of a glycolytic enzyme def? What is the result of a def in pyruvate dehydrogenase
RBC hemolysis

Neurologic defects
what is responsible for the release of renin?
JG apparatus, specifically the JG cells secrete it, while the macula densa senses the amount of Na
give the breakdown of your % body water
60% total body water
40% ICF
20% ECF
what is the water under the bridge idea?
ureters pass under the uterine artery or ductus deferens
CL=
UV/P

u-urine conc of X
p=plasma conc of X
v=urine flow rate
FF=?
GFR/RPF
GFR can be estimated with?

RPF?
GFR--creatinine

RPF--PAH
what segment of the renal tubule matches the following statement

reabsorbs 67% of fluid and electrolytes filtered by the glomerulus:

segment responsible for concentrating urine:

site of secretion of organic anions and cations:

always impermeable to water

permeable to water only in the presence of ADH
reabsorbs 67% of fluid and electrolytes filtered by the glomerulus: Prox tub

segment responsible for concentrating urine: Collecting duct

site of secretion of organic anions and cations: Prox

always impermeable to water: ascending loop

permeable to water only in the presence of ADH: collecting duct
what segment of the renal tubule matches the following statement

site of Na/2Cl/K cotransport:

site of isotonic fluid reabsorption:

site responsible for diluting urine:

only site where glucose and amino acids are reabsorbed:

water reabsorption in the loop of henle:
site of Na/2Cl/K cotransport: ascending loop

site of isotonic fluid reabsorption: prox tub

site responsible for diluting urine: thick ascending

only site where glucose and amino acids are reabsorbed: prox tub

water reabsorption in the loop of henle: thin descending
where are Ca and Mg reabsorbed? What happens with water here
Thick ascending limb

water cannot get in
where in the kidney does PTH have its effect on Ca?
leads to calcium reabsorption in the early distal tubule
what is the role of principle cells and intercalated cells? where does this occur
Principle: reabsorb H2O/Na, secrete K

Intercalated cells: secrete H/HCO3, reabsorb K

collecting duct
What are the 2 types of intercalated cells
Alpha: secrete Acid

Beta: secrete bicarb
what affect does aldosterone have on the intercalated cells and principle cells of the collecting duct?
intercalated: stimulates H secretion

principle: Na reabsorption and K secretion
tx for hyperkalemia?
Insulin to shift K into cells

must also give glucose to prevent hypoglycemia
what diuretic would you use for a woman with HTN and osteoporosis?
Thiazide

saves Ca
what is the acid base disorder

pH: 7.42
HCO3: : 32
pCO2: 64
Mixed

normal pH: 7.35-7.4
normal pCO2: 35-45
normal HCO3: 22
what is the acid base disorder

pH: 7.66
HCO3: 36
pCO2: 30
combined alk

normal pH: 7.35-7.4
normal pCO2: 35-45
normal HCO3: 22
what is the acid base disorder

pH: 7.10
HCO3: : 15
pCO2: 50
Combined acidosis

normal pH: 7.35-7.4
normal pCO2: 35-45
normal HCO3: 22
what is the acid base disorder

pH: 7.34
HCO3: : 31
pCO2: 62
resp acid with compensation

normal pH: 7.35-7.4
normal pCO2: 35-45
normal HCO3: 22
what is the acid base disorder

pH: 7.39
HCO3: : 12
pCO2: 22
mixed

normal pH: 7.35-7.4
normal pCO2: 35-45
normal HCO3: 22
what is the equation of anion gap?
Na - (Cl + HCO3)
what are the causes of increased anion gap
MUDPILES

Methanol (formic acid)
Uremia
Diabetic ketoacidosis
Paraldehyde/phenformin
Iron tablets or INH
Lactic acidosis
Ethylene glycol (oxalic acid)
Salicylates
where do type 1, 2, and 4 RTA occur? what are K levels like
1: distal (collecting tubule can't excrete H); hypokalemia

Type 2: proximal (defect in prox tubule HCO3 reabsorption); hypokalemia

type 3: hypoaldosteronism or lack of collecting tubule response to aldosterone, hyperkalemic
what effect will a renal stone that obstructs the ureter have on GFR and FF?
decrease both
what is the maximal serum glucose conc at which glucose can be absorbed in the tubules
350micro grams/dL
what change in the metabolic panel might you see in a young pt on a B-agonist for status asthmaticus?
B-agonists will lead to hypokalemia
What diuretic can be used in the following situations:

Edema a/w nephrotic syndrome:
Increased intracranial pressure:
Edema a/w nephrotic syndrome: Loop

Increased intracranial pressure: Mannitol
what type of diuretic are the following

Bumetanide:
Metolazone:
Bumetanide: Loop
Metolazone: Thiazide
if you have casts in the urine what does this tell you in general
that the problem is in the kidney
most common glomerular dz in HIV pts
FSGS
EM shows tram-track. what is this and what is it associated with?
type I MPGN--associated with HBV and HCV

(also: SLE, subacute bacterial endocardititis, mixed cryoglobulinemia)
EM shows dense deposits. What is this an what is it associated with?
MPGN type II

C3 nephritic factor
what 3 things can lead to using up complement?
Post strep
MPGN type II
SLE
which glomerular dz causes the following:

IF: granular pattern of immune complex deposition; LM: hyperceullar glomeruli:

LM: Segmental sclerosis and hyalinosis:
IF: granular pattern of immune complex deposition; LM: hyperceullar glomeruli: Acute post strep

LM: Segmental sclerosis and hyalinosis: FSGS
GLomerular histology reveals multiple mesangial nodules. What is this indicactive of?
Diabetic glomerulonephropathy
4 yo with facial edema and proteinuria. Tx?
this is MC

Corticosteroids
proteus causes stag horn calculi, what is the content of these stones
Ammonium magnesium phosphate
pt with gout or leukemia is likely to get what kind of kidney stone
uric acid
what happens in acute interstitial nephritis? what will you see? what is it due to?
acute renal failure
will see eosinophillia

due to drugs (1-2 weeks after administration

kids: ABX
adults: NSAIDs

tx: 2 weeks corticosteroids
+4 blood in urine, no RBC on urine cell count...
Rhabdomyolysis / myoglobinuria
what causes prerenal azotemia? what will BUN/Cr be like?
decreased RBF (hypotension: dehydration,shock,renal vasoconstriction, hepatorenal syndrome)

BUN/Cr >20 (BUN is really high because you are trying to hang on to everything)
what causes intrinsic renal failure? BUN/cr lvls?
acture tubular necrosis or ischemia/toxins

<15
what causes post renal azotemia? what is BUN/Cr like?
outflow obstruction (stones, BPH, neoplasia, congenital anomalies)

>15 (10-20, this is in a normal range)
sorry, i couldn't help myself...

what are the 2 most common causes of chronic kidney dz
HTN

Diabetes
ADPKD vs ARPKD

leads to potters:
hepatic fibrosis:
polycystic liver dz:
Berry aneurysms:
death can be due to malignant HTN:
leads to potters: AR
hepatic fibrosis: AR
polycystic liver dz: AD
Berry aneurysms: AD
death can be due to malignant HTN: (i had a question on this, it was an adult, and this is what killed him, so I am saying AD for now)
U waves on ECG is due to what
Low K
disoreintation stupor, or coma is assoc with what ion?
Na
pt is getting an infusion with substance X. Later the pt has decreased DTRs, delirium, and cardiopulmonary arrest. What was substance X
Mg
most common tumor of the urinary tract system?

histological appearance of renal cell ca?

histological appearance of chronic pyelonehpritis?

can assoc with schistosoma haematobium?
most common tumor of the urinary tract system: TCC

histological appearance of renal cell ca: Polygomal Clear Cell

histological appearance of chronic pyelonehpritis: Thyroidsim

can assoc with schistosoma haematobium: Bladder SCC
IF granular pattern of immune complex deposition; LM: diffuse capillary thickening
Membranous
IF granular pattern of immune complex deposition; LM: hypercellular glomeruli
Post strep glomerulinephritis
HYQ: CT scan reveals massively enlarged kidneys bilaterally. Diagnosis?
ADPCKD
what is responsible for the biconcave shape and flexibility of RBCs
spectrin
Anisocytos=

Poikilocytosis=
Anisocytos= varying RBC size

Poikilocytosis= varying RBC shape
survival time of RBCs?

platelets?
RBC=120

Platelets=8-10

days
what is the DNAAACP for eosinophils
Drugs
Neoplasm
Asthma
Allergic process
Addisons
Collagen vascular dz
Parasites
what type of cell are barr bodies in?
Neutrophils
What are the phagocytes for the following locations:

Brain:
Liver:
Joint:
Lung:
Brain: microglia
Liver: kupffer cell
Joint: A cells
Lung: Dust cells
what cell traditionally has memory and plays a role in immunizations

*
B lymphocyte
what is the bridge btw coagulation and complement pathway
factor XII
why do you get purple toes etc with starting Warfarin
while warfarin will eventually inhibit 10,9,7,2, they accutely inhibit C and S leading to hypercoaguability

give Heparin for first few days to prevent this
MOA of heparin
inhibits thrombin (factor II)

co factor of antithrombin

ACTIVATES ANTITHROMBIN WHICH IN TURN INHIBITS THROMBIN
warfarin or heparin

which if either can be used in pregnancy
Heparin
pt is on anticoagulant and develops thrombocytopenia which was it?

Tx? MOA?
heparin- Heparin induced thrombocytopenia (causes hypercoaguable state)

Lepiruidn or bivalirudin--directly inhibit thrombin
what drug inhibits ADP induced expression of GpIIb/IIIa
Clopidogrel

Ticlopidine
what are the following RBCs seen in

Basophilic stippling:

Bite Cells:

Schistocyte/helmet cell:

Target Cells:

Heinz bodies:

Howell-Jolly bodies:
Basophilic stippling: Lead

Bite Cells: G6PD

Schistocyte/helmet cell: DIC/TTP/HUS/traumatic hemolysis

Target Cells: HbC dz, Asplenia, liver dz, thalassemia (THAL)

Heinz bodies: G6PD def

Howell-Jolly bodies: asplenia (sickle cell, ITP, splenic trauma)
what is the change in the Hb of sickle cell
Glu-->Val in B chain
4 causes of microcytic hypochromic anemia...what is the MCV
MCV<80

Iron def
Thalassemia
Lead poisoning
sideroblastic

CKD -apparently starts normocytic
marrow hyperplasia leading to chipmunk facies and crew cut xray
B-thal major
tx for lead poisoning in adults/kid
adult: dimercaprol

kid: succimer
hypocellular bone marrow with fatty infiltration....
Aplastic anemia

(pancytopenia--anemia, neutropenia, and thrombocytopenia)
if you have sickle cell or hereditary spherocytosis, what can lead to aplastic crisis?
parvo B19
what can you use in the treatment of sickle cell anemia?
Hydroxyurea to increase HbF

bone marrow transplant is curative
what are the 5 causes of megaloblastic anemia
Methotrexate
AZT
Phenytoin
Liver dz
Ethanol

MAPLE
what is the cause of anemia given the following statement:

Microcytic anemia reversible with B6:

HIV positive pt with macrocytic anemia:

normocytic anemia and elevated creatinine :
Microcytic anemia reversible with B6: sideroblastic anemia

HIV positive pt with macrocytic anemia: Zidovudine

normocytic anemia and elevated creatinine : kidney failure
pt presents with painful abdomen, port red urine, polyneuropathy, and psychological disturbances. What is this and what drug might they be on? enzyme affected
Acture intermittent porphyria

Barbiturates

porphobilinogen deaminase
man presents with blisters on sun exposed areas of his body and he has darkening of his face with a large amount of hair. What does he have? affected enzyme?
Porphyria cutanea tarda

Uroporphyrinogen decarboxylase
decreased Gp1b-->defect in platelet to collagen adhesions
Bernard soulier dz
GpIIb/IIIa antibodies-->peripheral platelet destruction
Idiopathic thrmobocytopenic purpura (ITP)
decreased GpIIb/IIIa -->defect in platelet to platelet aggregation
Glanzmann's thrombasthenia
pt has neurologic and renal sx, fever, thrombocytopenia, and microangiopathic hemolytic anemia...what does he have? what is deficient?
Thrombotic thrombocytopenic purpura (TTP)

def of ADAMTS 13 (vWF metalloprotease)-->degrades vWF thrombosis
what are some of the causes of DIT
STOP Making New Thrombi

Sepsis (G-)
Trauma
Obstetric
Pancreatitis
Malignancy
Nephrotic syndrome
Transfusion
What is the rate-limiting step in heme synthesis
aminolevulinic acid synthase
what are the following tests associated with:

Hams:
DEB:
Heinz body:
D-Dimer:
Basophilic stippling:
Osmotic fragility test:
(+) ristocetin test:
Hams: Paroxsymal nocturnal hemoglobinuria
DEB: Fanconi's anemai
Heinz body: G6PD
D-Dimer: DIC
Basophilic stippling: Thalassemia, ACD, Iron def, LEAD POISONING
Osmotic fragility test: hereditary spherocytosis
(+) ristocetin test: vWF dz
Hodgkin vs Non-Hodgkin

Reed-Sternberg Cells
Bimodal distribution:
Assoc with HIV
B symptoms:
Mostly involves B cells:
Peripheral nodes, noncontiguous spread:
Local nodes: contiguous spread:
Reed-Sternberg Cells: H
Bimodal distribution: H
Assoc with HIV: NH
B symptoms: H
Mostly involves B cells: NH
Peripheral nodes, noncontiguous spread: NH
Local nodes: contiguous spread: H
what is the most common type of AML and the translocation associated?
M3 type

t(15,17)
Leukemia buzzwords:

Smudge cell:
Children:
TRAP:
Philadelphia chromosome:
Auer Rods:
Smudge cell: CLL
Children: ALL
TRAP: Hairy cell
Philadelphia chromosome: CML
Auer Rods: AML
What is most likely to cause progression to AML
CML
What drug targets the Philadelphia chromosome? what is this treating?
Imatinib

CML
what leukemia/lymphoma is most likely to cause bone pain
ALL
Birbeck granules ("tennis rackets" on EM)
Langerhans cell histiocytosis
woman says she itches when she is in the shower. She says she has pain in her hands/fingers that is relieved with aspirin. what does she have
polycythemia vera
give the hematological dz that matches the following:

AML assoc with Downs:

Leukemia with more mature cells and less than 5% blasts:

PAS + acute leukemia:
AML assoc with Downs: M7 AML (ALL is most common)

Leukemia with more mature cells and less than 5% blasts: Chronic leukemia

PAS + acute leukemia: ALL
give the hematological dz that matches the following:

Greater than 20% blasts in marrow:

myleodysplastic/proliferative disorders may progress to:

numerous basophils, splenomegaly, and negative for leukocyte alkaline phosphatase (LAP):
Greater than 20% blasts in marrow: acute leukemia

myleodysplastic/proliferative disorders may progress to: AML

numerous basophils, splenomegaly, and negative for leukocyte alkaline phosphatase (LAP): CML
give the hematological dz that matches the following:

most common neonatal leukemia:

associated with the BCR-ABL genes:

assoc with sjogren, hashimoto's thyroiditis, and h pylori:
most common neonatal leukemia: M7 AML

associated with the BCR-ABL genes: CML

assoc with sjogren, hashimoto's thyroiditis, and h pylori: Marginal cell MALToma
give the hematological dz that matches the following:

acute leukemia positive for peroxidase:

solid sheets of lymphoblasts in marrow:

PAS (-) acute leukemia:
give the hematological dz that matches the following:

acute leukemia positive for peroxidase: AML

solid sheets of lymphoblasts in marrow: ALL

PAS (-) acute leukemia: AML
describe the following in DIC

BT:
PT:
PTT:
Platelet count:
BT: increase
PT: increase
PTT: increase
Platelet count: decrease
HYQ: 11 year old child presents with a chronic non-healing ulcer on his foot and imaging shows a small calcified spleen. What drug can improve his sx?
This is sickle cell

Hydroxyurea