PATH RENAL Flashcards

1
Q

RBC cast indicate

A

Glomerulonephritis, hypertensive emergency

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2
Q

WBC cast indicate

A

Tubulointerstitial inflammation, acute pyelonephritis and transplant rejection

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3
Q

Granular cast indicate

A

Acute tubular necrosis- muddy brown appearance

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4
Q

Fatty cast indicate “ oval fat bodies”

A

Nephrotic syndrome- Associated with Maltase cross” sign

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5
Q

Waxy cast indicate

A

End stage renal disease/ chronic kidney disease

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6
Q

Hyaline cast indicate

A

Can be normal

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7
Q

What is thrombotic thrombocytopenic purpura (TTP)?

A

A condition characterized by deficiency of ADAMTS13, leading to platelet aggregation triggered by accumulation of large multimers of vWF.

TTP can be inherited or acquired.

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8
Q

What triggers platelet aggregation in TTP?

A

Accumulation of large multimers of vWF.

vWF stands for von Willebrand Factor.

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9
Q

What are the key clinical features (C/F) of TTP?

A

PENTAD:
* Neurologic symptoms
* Fever
* Thrombocytopenia
* Hemolysis (microangiopathic hemolytic anemia)
* Kidney failure

The mnemonic for remembering these features is ‘nasty fever torched his kidneys’.

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10
Q

What does the term ‘thrombocytopenia’ refer to?

A

A condition characterized by low platelet count.

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11
Q

What type of anemia is associated with TTP?

A

Microangiopathic hemolytic anemia.

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12
Q

What is a common renal complication in TTP?

A

Kidney failure, cortical necrosis, and sub-capsular petechia.

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13
Q

What is the characteristic appearance of the basement membrane in TTP?

A

Double contour or tramtrack appearance.

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14
Q

What metalloprotease is deficient in TTP?

A

ADAMTS13.

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15
Q

What happens to ‘ultralarge’ TTP multimers in the presence of ADAMTS13?

A

They are normal and not degraded.

Ultralarge multimers of vWF are typically associated with increased platelet aggregation.

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16
Q

Where are microthrombi found in TTP?

A

In glomerular and interstitial capillaries.

17
Q

What is diffuse cortical necrosis?

A

A complication seen in TTP characterized by widespread death of kidney cortex tissue.

19
Q

What is the typical form of hemolytic uremic syndrome (HUS) associated with?

A

Diarrhea-positive Escherichia coli strain 0157:H7 intestinal infection

Typical HUS is also known as epidemic or classic HUS.

20
Q

What toxin does the typical HUS strain elaborate?

A

Shiga-like toxin (stx)

This toxin is responsible for the pathogenesis of typical HUS.

21
Q

What receptor does Stx bind to in the pathogenesis of typical HUS?

A

Globotriasylceramide GB3 receptor

This receptor is primarily found on the renal endothelium.

22
Q

What are the consequences of Stx binding to the GB3 receptor?

A
  • Damage to the endothelium
  • Platelet activation and vasoconstriction
  • Formation of microthrombi
  • Vascular obstruction & tissue ischemia
  • Shearing of RBCs
  • Schistocytes and thrombocytopenia

These processes contribute to the symptoms observed in HUS.

23
Q

What characteristic appearance is associated with the basement membrane in HUS?

A

Rouble contour or tramtrack appearance

This appearance is noted in the context of endothelial damage.

24
Q

What defines atypical HUS?

A

Non-epidemic, diarrhea-negative

Atypical HUS has different underlying mechanisms compared to typical HUS.

25
What causes the impaired function of complement regulatory proteins in atypical HUS?
Inherited conditions or autoantibodies ## Footnote This impairment can lead to atypical HUS.
26
What deficiency is associated with atypical HUS?
Factor H deficiency ## Footnote Factor H is a regulatory protein involved in the complement system.
27
What conditions are associated with atypical HUS?
* Antiphospholipid antibody syndrome * Nephrosclerosis ## Footnote These conditions can contribute to the development of atypical HUS.
28
What is the prognosis for atypical HUS?
Relatively bad ## Footnote Atypical HUS tends to have a poorer prognosis compared to typical HUS.
29
What is observed in the capillaries in atypical HUS?
Microthrombi ## Footnote These microthrombi can be identified using fibrin staining.