RENAL DISEASE Flashcards

1
Q

ETIOLOGY:
Cellular proliferation affects the
capillary walls or the glomerular
basement membrane, possibly immune-mediated

A

MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS

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2
Q

ETIOLOGY:
Marked decrease in renal function resulting from glomerular damage precipitated by other renal disorders

A

CHRONIC GLOMERULONEPHRITIS

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3
Q

SIGNIFICANT TESTS FOR CHRONIC GLOMERULONEPHRITIS:

A

BUN, SERUM, CREATININE, eGFR, ELECTROLYTES

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4
Q

ETIOLOGY:
Deposition of IgA on the glomerular membrane resulting from increased levels of serum, IgA

A

IMMUNOGLOBULIN A NEPHROPATHY (BERGER’S DISEASE)

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5
Q

ETIOLOGY:
Disruption of the shield of negativity and damage to the tightly fitting podocyte barrier resulting in massive loss of protein and lipids

A

NEPHROTIC SYNDROME

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6
Q

SIGNIFICANT TESTS FOR NEPHROTIC SYNDROME:

A

Serum albumin, Cholesterol, Triglycerides

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7
Q

ETIOLOGY:
Disruption of the podocytes occurs primarily in children following allergic reactions and immunizations

A

MINIMAL CHANGE DISEASE (LIPID NEPHROSIS)

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8
Q

ETIOLOGY:
Disruption of podocytes in certain areas of glomeruli associated with heroin and analgesic abuse and AIDS

A

FOCAL SEGMENTAL GLOMERULOSCLEROSIS

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9
Q

ETIOLOGY:
Damage to renal tubular cells caused by ischemia or toxic agents

A

ACUTE TUBULAR NECROSIS

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10
Q

ETIOLOGY:
Inherited in association with cystinosis and Hartnup disease of acquired through exposure to toxic agents

A

FANCONI SYNDROME

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11
Q

ETIOLOGY:
Genetic disorder showing lamellated and thinning glomerular basement membrane

A

ALPORT’S SYNDROME

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12
Q

ETIOLOGY:
Inherited defect of tubular response to ADH or acquired from medications

A

NEPHROGENIC DIABETES INSIPIDUS

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13
Q

TYPE OF NEPHROGENIC DIABETES INSIPIDUS:
- Failure of tubules to respond to
antidiuretic hormone (ADH), inherited sex-linked recessive or lithium and amphotericin B
exposure, polycystic kidneys and sickle cell
anemia

A

NEPHROGENIC

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14
Q

TYPE OF NEPHROGENIC DIABETES INSIPIDUS:
- Failure to produce ADH

A

NEUROGENIC

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15
Q

ETIOLOGY:
Inherited autosomal recessive trait
Other significant test: Blood Glucose

A

RENAL GLYCOSURIA

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16
Q
  • Formerly Tamm-Horsfal protein was the only protein produced by the kidney
  • Inherited disorder that results in an abnormal buildup of uromodulin in the
    tubular cells causing their destruction
A

UROMODULIN-ASSOCIATED KIDNEY
DISEASES (UMKD)

17
Q

ETIOLOGY:
Infection of the renal tubules and interstitium related to interference of urine flow to the bladder, reflux of urine form the bladder

A

ACUTE PYELONEPHRITIS

18
Q

ETIOLOGY:
Recurrent infection of the renal tubules and interstitium caused by structural abnormalities affecting the flow of urine

A

CHRONIC PYELONEPHRITIS

19
Q

ETIOLOGY:
Allergic inflammation of the renal interstitium in response to certain medications

A

ACUTE INSTERSTITIAL NEPHRITIS

20
Q

o Decreased blood pressure/cardiac output
o Hemorrhage
o Burns
o Surgery
o Septicemia

A

PRE-RENAL

21
Q

o Acute glomerulonephritis
o Acute tubular necrosis
o Acute pyelonephritis
o Acute interstitial nephritis

A

RENAL

22
Q

o Renal calculi
o Tumors
o Crystallization of ingested substances

A

POST-RENAL

23
Q

 Progression from original disorders to end-stage renal disease
 GFR <25 mL/min, 11 BUN and creatinine levels, electrolyte imbalance, isosthenuria, proteinuria, renal gycosuria; 1 granular, waxy, broad casts

A

CHRONIC RENAL FAILURE

24
Q

 Sudden onset, often reversible
 Decreased blood flow (prerenal), acute disease (renal), renal calculi and tumors (postrenal)

A

ACUTE RENAL FAILURE

25
Q

 Renal calculi (kidney stones) in calyces and pelvis of kidney, ureters, bladder
 Staghorn, round and smooth, barely seen
 Severe back pain radiating from lower back to legs when passing

A

RENAL LITHIASIS