Renal Pathology Flashcards

1
Q

What are the warning signs of kidney disease?

A

A Cr and BUN outside the normal range, GFR less than 60, blood and/or protein in the urine, HTN, more frequent urination particularly at night (difficult or painful urination), puffiness around the eyes, swelling of the hands and feet

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2
Q

What are the principle fluid and electrolyte manifestations of acute or chronic kidney dysfunction?

A

dehydration, edema, hyperkalemia, metabolic acidosis

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3
Q

What are the principle Ca, phosphate and bone manifestations of acute or chronic kidney dysfunction?

A

Hyperphosphatemia, hypocalcemia, secondary hyperparathyroidism, renal osteodystrophy

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4
Q

What are the principle hematologic manifestations of acute or chronic kidney dysfunction?

A

anemia, bleeding diathesis

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5
Q

What are the principle cardiopulmonary manifestations of acute or chronic kidney dysfunction?

A

HTN, CHF, cardiomyopathy, pulmonary edema, uremic pericarditis

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6
Q

What are the principle GI manifestations of acute or chronic kidney dysfunction?

A

N/V, bleeding, esophagitis/gastritis/colitis

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7
Q

What are the principle neuromuscular manifestations of acute or chronic kidney dysfunction?

A

myopathy, peripheral neuropathy, encephalopathy

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8
Q

What are the principle dermatologic manifestations of acute or chronic kidney dysfunction?

A

sallow color, pruritus, dermatitis

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9
Q

What is the ideal ratio of BUN to Cr?

A

Between 10 to 1 and 20 to 1

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10
Q

What is usually a manifestation of subtle or mild glomerular abnormalities?

A

asymptomatic hematuria or proteinuria, or a combination of these two

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11
Q

What causes pre-renal azotemia?

A

CHF, burns, hemorrhage in GIT, shock and stress, dehydration

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12
Q

What causes renal azotemia?

A

glomerulonephritis, pyelonephritis, DM, nephrotoxic drugs, renal failure, anabolic steroids use

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13
Q

What causes post renal azotemia?

A

urinary tract obstruction (stones, neoplasms, bladder or urethral abnormality, bladder outlet obstruction)

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14
Q

What are the 3 sites where constrictions in the ureters normally appear?

A

at the ureteropelvic junction, crossing the external iliac A and/or pelvic brim, as the ureter traverses the bladder wall

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15
Q

What can cause tubulointersitial nephritis?

A

Infections (acute or chronic bacterial pyelonephritis, other infections), toxins, metabolic disease (urate nephropathy, nephrocalcinosis, oxalate nephropathy), physical factors (chronic urinary tract obstruction, neoplasms, multiple myeloma), immunologic reactions, vascular diseases

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16
Q

What is the empiric treatment for an uncomplicated UTI caused by proteus?

A

outpatient treatment with either a 3 day course of trimethoprim/sulfamethoxazole (TMP/SMZ) or an oral fluoroquinolone (ciprofloxacin)

17
Q

What is the treatment for a pt presenting with complicated UTI (e.g. pt with an underlying condition that may increase the risk of failure of therapy)?

A

May be treated in an outpatient setting with oral abx for 10-21 days as log as they receive adequate follow up

18
Q

Acute uncomplicated pyelonephritis can be treated on an outpatient basis with what abx?

A

Fluoroquinolone although a regimen of 7-14 days is recommended; an alternative to this treatment is a one time dose of ceftriaxone or gentamicin followed by either TMP/SMZ, an oral fluoroquinolone or cephalosporin for 7-14 days

19
Q

What is the function of uromodulin (Tamm-Horsfall protein)?

A

Multifunctional protein critical for modulating renal ion channel activity, salt/water balance, renal and systemic inflammatory responses, intertubular bacterial adhesion

20
Q

Mutations in Tamm-Horsfall cause what?

A

a group of inherited kidney diseases and altered THP expression is associated with increased risks of UTI, kidney stones, HTN, hyperuricemia, and acute/chronic kidney disease

21
Q

What is hepatorenal syndrome?

A

A form of renal failure occurring in individuals with liver failure in whom there is no intrinsic morphologic or functional cause for kidney dysfunction

22
Q

The onset of hepatorenal syndrome is marked by what?

A

a drop in urine output and increasing levels of urea and Cr in the blood

23
Q

What is the triggering event of hepatorenal syndrome?

A

Portal HTN and secondary increased production of vasodilators such as NO by endothelial cells in the splanchnic vasculature which leads to systemic vasodilation and diminished renal perfusion which is sensed by the kidney provoking activation of RAAS –> renal failure