Tubular Disease Flashcards

1
Q

What cell does acute tubular necrosis affect?

A

Renal tubular epithelial cells.

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2
Q

What happens to renal tubular epithelial cells during acute tubular necrosis?

A

Results in the destruction of the renal tubular epithelial cells.

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3
Q

What are the two ways acute tubular necrosis can occur?

A

(1) Ischemia condition (obstruction of blood flow)
(2) Toxic processes

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4
Q

What are the three causes of ischemic acute tubular necrosis?

A

(1) Sepsis
(2) Shock
(3) Trauma

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5
Q

Ischemic acute tubular necrosis effects what parts of the nephron?

A

The basement membrane and the tubules.

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6
Q

Toxic acute tubular necrosis can either result in what two processes?

A

Endogenous or Exogenous.

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7
Q

What is the endogenous process for a patient with toxic acute tubular necrosis?

A

These solutes or substances are when the concentration in the blood becomes too high, becoming toxic.

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8
Q

Give an example of an endogenous process for a patient with toxic acute tubular necrosis.

A

Hemoglobin or myoglobin after a trauma or hemolytic episode.

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9
Q

What is the exogenous process for a patient with toxic acute tubular necrosis?

A

Chemicals or substances that we take into the body.

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10
Q

Give an example of an exogenous process for a patient with toxic acute tubular necrosis.

A

Antibiotics, anesthetics, and radio contrast media.

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11
Q

What would you expect to find on a urinalysis chemical test for a patient with acute tubular necrosis?

A

Positive blood and protein; low specific gravity.

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12
Q

What would you expect to find on a urinalysis microscopic test for a patient with acute tubular necrosis?

A

Renal tubular cells present; renal tubular, waxy, broad, granular casts present.

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13
Q

How do hereditary and metabolic tubular dysfunction affect the tubules?

A

Via a build-up of metabolic by-products that the tubules can no longer reabsorb.

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14
Q

What causes Fanconi syndrome?

A

A build-up of amino acids as well as glucose, phosphate, sodium, and potassium that can be found in the urine.

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15
Q

What is Fanconi syndrome?

A

A proximal tubular dysfunction where substances cannot be reabsorbed and get excreted into the urine.

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16
Q

Fanconi syndrome can be an inherited disorder or the result of what?

A

Toxin exposure, metabolic disease, or secondary to renal disease.

17
Q

Cystinosis and cysinuria affects which functional part of the kidney?

A

Can affect the tubular function.

18
Q

Cystinosis and cysinuria is an autosomal recessive disorder that results in what condition?

A

Tubular dysfunction causing an excess amount of cystine to be excreted into the urine.

19
Q

Renal glucosuria is a benign inherited condition that does what?

A

Have lower tubular reabsorptive capacity resulting in glucose being present in the urine.

20
Q

Renal phosphaturia is an inherited disorder that effects what part of the kidney?

A

Distal tubules.

21
Q

Renal phosphaturia is an inherited disorder does what?

A

Causes a dysfunction of the distal tubules where it does not allow for organic phosphorous to reabsorbed.

22
Q

What are some clinical symptoms a patient may have who has renal phosphaturia?

A

May range from being asymptomatic to having shunted growth.

23
Q

What occurs with a patient with renal tubule acidosis?

A

In this inherited autosomal disorder, patients are unable to adequately secrete hydrogen ions or reabsorb bicarbonate ions in the proximal tubules.