Renal Path Flashcards

1
Q

What controlls blood flow into the bowmans capsule and how does NSAIDs change it (afferent)

A

controlled by PGE2 (vasodialater)

-NSAIDs reduce PGE2- lead to vasoconstriction of afferent arteriole and increased risk of ischemic damage to the medulla

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2
Q

What controlles effect of bowmans

A

Angiotensin type 2 (contractor)

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3
Q

Renal functions

A
Excrete harmful waste products
maintain acid base homeostasis 
reabsorb essential substances
Regulate water/sodium
maintain vascular tone
produce erythropoietin
calcium homeostasis
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4
Q

Generalized signs of kidney pathology (+mc)

A

blood in urine (mc)*

  • Abdominal swelling
  • stroke
  • fever
  • itching
  • thirst
  • tiredness
  • chest pain
  • weight gain
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5
Q

Major clinical manifestations of renal diseases

A

Proteinura

Azotemia (elevation of Blood Urea nitrogen and createin levels as a result of decreased GFR)

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6
Q

What is pre renal azotemia and cause

A

cause: decreased cardiac
- patient loses ability to perfuse kidney structures-> leads to decreased GFR

*There will be no intrinsic renal parenchymal disease (will return to normal once cause is treated)

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7
Q

What is post renal azotemia + causes

A

Urinary tract obstruction below the kidney (prostate hyperplasia, ureter block, tumor)

-initially no renal parenchymal disease, but over time will (causes increased tubular pressure causes back diffusion of urea into the blood)

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8
Q

What is renal azotemia

A

Caused by parenchymal to kidney (acute tubular necrosis, chronic renal failure)

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9
Q

What are other minifistations of renal diseases other than proteunuria and azotemia

A
  • Hematuria
  • urinary mucrospoic changes
  • hypertension
  • electrolyte disorders
  • casts
  • oliguria/anuria/polyyria
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10
Q

What is renal agenesis

A

-Absence of one or both kidneys (bilateral deadly)

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11
Q

What is renal hypoplasia

A
  • Usually unilateral

- presence of underdeveloped kidney unilat, other side is normall/fully developed kidney

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12
Q

What is horeshoe kidney and what is it associated with

A
  • one of the mc kidney abnormalities
  • kidney fusion of lower pole usually
  • associated with turners syndorme
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13
Q

What is ectopic kidney/renal ectopia- and what can the symptoms mimic/what are you predisposed to

A

birth defect where kidney develops normally but is located below or above or contralateral of its usual pos

  • symptoms may mimic urinary tract obstruction
  • predisposed to pyleonephritis
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14
Q

What is a duplex kidney

A

they duplex kidney has a single renal parenchyma that is drained by 2 pyelocaalceal systems

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15
Q

What is autosmal recescive polycystic kidney- age, cause

A

dx in infnacy

-disorder is linked to an abnormal fibrocystic protein produced by the PKHD1 gene

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16
Q

Autosomal dominant polycystic kidney- age, caue

A

Autosomal dominant inheritance

-mc polycystic kidney disease 1 (PKD1) gene mutation

17
Q

Clinical manisfitations of atosomal dominant kidney

A

Asymptomatic with norma; renal functins until middle age (delop slowly over time)

-hematuria, hypertension, abdominal mass (bilaterally) etc

18
Q

What is renal dysplasia- etiology, pathophysiology

A

genetic
iatrogenic- mutation cased by ACE inhibitors and angiotension receptor blockers

  • the tubules fail to branch out and urine has nowhere to go
  • the urine collects inside the kidney and forms cysts
19
Q

What is medullary sponge kidney kidney

A

Benign congenital disorder
-characterized by dialation of collecting tubules in 1 or more renal papillae affecting 1 or both kidneys

-usually asymptomatic (can rarely lead to chronic kidney disease/renal failure)

20
Q

Wht is acuired cystic kidney disease and how do u get it

A

consequence of hemodialysis

21
Q

3 stages of aquired cystic disease

A
  1. Tubue block- development of cysts is due to tubular abnormalities
  2. Compensatory growth- profound loss of renal tissue in endstage kidney disease promotes tubular cell hypertrophy and hyperplasia. Growth factors and activation of oncogenes
  3. Ishemia- kidney atrophy
22
Q

What is simple retention cysts

A

Arise from glands by retention of their secreteion due to obstruction or obliteration of the ducts

-obstruction of the urinary duct can cause a kidney retention cyst