syd renal patho

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Last updated 4:05 AM on 7/30/26
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46 Terms

1
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How is Adult Polycystic Kidney Disease inherited?

Autosomal dominant

2
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How is Childhood Polycystic Kidney Disease inherited?

Autosomal recessive

3
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When do signs of renal failure manifest clinically in patients with Adult Polycystic Kidney Disease?

30s-40s

4
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When do signs of renal failure manifest clinically in patients with Childhood Polycystic Kidney Disease?

Newborn period

5
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What conditions are associated with Adult Polycystic Kidney Disease?

Berry aneurysms and liver cysts

6
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Which congenital kidney disorders can lead to a Potter's sequence?

Bilateral agenesis or cystic dysplasia

7
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What facial features are associated with the Potter sequence?

Prominent infraorbital folds, low-set ears, small receding chin, & flattened nose

8
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What extremity features are associated with the Potter sequence?

Redundant skin folds of the hands & abnormally bent lower extremities (club feet)

9
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What is the #1 cause of death in infants with Potter's sequence?

Pulmonary hypoplasia

10
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What is the most common cystic congenital renal disease?

Renal cystic dysplasia

<p>Renal cystic dysplasia</p>
11
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What is the most common non-cystic congenital renal disease?

Horseshoe kidney

<p>Horseshoe kidney</p>
12
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What are the 3 components of the glomerular filtration membrane?

Fenestrated capillary endothelium (CL), glomerular basement membrane (BM), & podocytes (US)

<p>Fenestrated capillary endothelium (CL), glomerular basement membrane (BM), &amp; podocytes (US)</p>
13
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What are the four types of kidney stones?

Calcium, Struvite, Uric Acid, and Cysteine

14
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What is the most common type of kidney stone?

Calcium stones

15
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What is another name for a struvite stone?

Triple stones

16
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Which of the types of kidney stones are associated with Proteus converting ammonia from urea?

Struvite stones (Staghorn Calculi)

17
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What term is used to describe dilation of the renal pelvis and calyces associated with progressive atrophy of the kidney due to obstruction to the outflow of urine?

Hydronephrosis

<p>Hydronephrosis</p>
18
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What are possible causes of hydronephrosis?

Kidney stones, BPH, tumors

19
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What happens to the transitional epithelium of the renal pelvis and calyces in hydronephrosis?

Becomes paper-thin

20
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What are urinalysis findings in acute cystitis and acute pyelonephritis?

Presence of bacteria, pus, and WBCs

21
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What causes the formation of WBC casts in the urine?

Stacking of neutrophils in the tubules

22
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Where are renal cell carcinomas located?

Upper or lower poles of the kidney

23
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What are transitional cell carcinomas located?

Hilus of the renal pelvis

24
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What is Wilms tumor?

A genetic, embryologic kidney cancer that occurs in children

25
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What is the prognosis for Wilms tumors?

Good if detected before metastasis

26
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How are Wilms tumors diagnosed histologically?

Metanephric blastic tissue must be present

27
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What is the most important risk factor for both RCC and transitional cell carcinomas?

Cigarette smoking

28
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Are RCC and urinary bladder cancers more common in men or women?

Men

29
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Between RCC and urinary bladder cancers, which is two times more common than the other, but accounts for the same number

of deaths?

Urinary bladder cancer

30
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What causes the yellow/orange color of RCC grossly?

Increased glycogen

<p>Increased glycogen</p>
31
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What is the classic triad of RCC clinically?

Hematuria, dull flank pain, & palpable abdominal mass

32
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What is the prototype glomerular nephritic syndrome?

Acute Post-Streptococcal Glomerulonephritis

33
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What characterizes a nephritic syndrome?

Spilling RBCs into the urine

34
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What characterizes a nephrotic syndrome?

Spilling protein into the urine

35
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What does granularity of the basement membrane on immunofluoresence microscopy indicate?

Presence of immune complexes

36
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What is the #1 immune complex nephritic syndrome?

Acute Post-Streptococcal Glomerulonephritis

<p>Acute Post-Streptococcal Glomerulonephritis</p>
37
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What is the most immune complex nephrotic syndrome in adults?

Membranous Glomerulonephritis

38
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What is another name for crescentic glomerulonephritis?

Rapidly Progressive Glomerulonephritis

<p>Rapidly Progressive Glomerulonephritis</p>
39
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Is what renal condition are RBC casts present in the urine?

Acute post-streptococcal glomerulonephritis

<p>Acute post-streptococcal glomerulonephritis</p>
40
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What is the most common cause of nephrotic syndrome in children?

Minimal Change/Nils Disease

41
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Which glomerular disease causes nephrotic syndrome without a nephritic syndrome as well?

Minimal Change/Nils Disease

42
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What are the characteristic histologic findings in membranous glomerulonephritis?

Thickening of the GBM with deposition of granular immune complexes

43
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What is the etiology of renal papillary necrosis?

Ischemia & infection

44
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In what patients is renal papillary necrosis usually seen?

Diabetics with acute pyelonephritis

45
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What is the only way to diagnose Minimal Change/Nils Disease?

Scanning EM

46
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What findings are present on scanning EM in Minimal Change/Nils Disease?

Flattening of podocyte foot processes, absence of immune deposits, & normal GBM