renal disorders Flashcards

1
Q

this renal disorder is formed in the conjunction with GROUP A STREPTOCOCCUS

a. acute glomerulonephritis
b. rapidly progression glomerulonephritis
c. good pasteur’s syndrome

A

acute glomerulonephritis

  • GROUP A STREPTOCOCCUS
  • ASO
  • ANTI - GROUP A STREPTOCOCCUS
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2
Q

attachment of cytotoxic antibody formed during viral respiratory infections

a. acute glomerulonephritis
b. rapidly progression glomerulonephritis
c. good pasteur’s syndrome

A

good pasteur’s syndrome
- -attachment of CYTOTOXIC ANTIBODY formed during viral respiratory infections to glomerular and ALVEOLAR BASEMENT MEMBRANES

- ANTI GLOMERULAR BASEMENT MEMBRANE ANTIBODY
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3
Q

ANTI GLOMERULAR BASEMENT MEMBRANE ANTIBODY

a. acute glomerulonephritis
b. rapidly progression glomerulonephritis
c. good pasteur’s syndrome

A

c. good pasteur’s syndrome

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4
Q

ANTINEUTROPHILIC cytoplasmic autoantibody binds to NEUTROPHILS in vascular walls

a. wegener’s granulomatosis
b., henoch schonleinpurpura
c, IgA nephropathy

A

wegener’s granulomatosis
!!! neutrophil!!!

-antineutrophilic cytoplasmic antibody (ANCA)

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5
Q

occurs primarily in CHILDREN ; a DECREASE IN PLATELETS disrupt the vascular integrity

a. wegener’s granulomatosis
b., henoch schonleinpurpura
c, lipid nephrosis

A

henoch schonleinpurpura
- !!decrease platelets!!!!!!!!!!!!!!!!!!!!!

-stool occult blood

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6
Q

this disease required to performthe test STOOL OCCULT BLOOD

a. burger’s disease
b. henoch scholeinpurpura
c. wegener’s granulonephritits

A

henoch schonleinpurpura

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7
Q

thickenng of the glomerular membrane following IgG immune complex deposition associated with systemic disorders

a. IgA nephropathy
b. membranous glomerulonephritis
c. wegener granulomatosis

A

membranous glomerulonephritis

- IgG

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8
Q

tram truck of pattern of the glomerulus

a. membranous glomerulonephritis
b. membranoproliferative glomerulonephritis
c. chronic glomerulonephritits

A

membranoproliferative glomerulonephritis

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9
Q

MARKED DECREASE IN RENAL FUNCTION resulting from glomerular damage

a. membranous glomerulonephritis
b. membranoproliferative glomerulonephritis
c. chronic glomerulonephritits

A

chronic glomerulonephritis

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10
Q

disruption of electrical charges that produces tightly fitting podocytes

a. nephrotic syndrome
b. alport syndrome
c. diabetic nephropathy

A

nephrotic syndrome

- disruption of electrical charges  or called shield of negativity
- tightly fitting podocytes
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11
Q

disruption of podocytes occurs primarily in CHILDREN following ALLERGIC REACTIONS AND IMMUNIZATION

a. lipid nephrosis
b. focal segmental glomerulosclerosis
c. alport syndrome

A

minimal change disease ( Lipid Nephrosis)

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12
Q

disruption of podocytes in CERTAIN AREAS OF GLOMERULI ASSOCIATED WITH HEROIN AND ANALGESTIC ABUSE and acquired immunodeficiency disease

a. lipid nephrosis
b. focal segmental glomerulosclerosis
c. alport syndrome

A

focal segmental glomerulonephritis

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13
Q

significant test for focal segmental gloemerulosclerosis

a. drug of abuse
b. triglycerides
c. hiv tests
d. fta-abs

A

focal segmental glomerulosclerosis

 - drug of abuse
 - hiv tests

membranous gloemrulonephritis

  - FTA ABS
  - antinuclear  antibody
  - hepatitis surface antigen
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14
Q

genetic disorder showing LAMELLATED AND THINING OF GLOMERULAR BASEMENT MEMBRANE

a. focal segmental glomerulosclerosis
b. lipid necrosis
c. alport syndrome

A

alport syndrome

- lamellated and thining membrane

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15
Q

most common End stage renal disease

a. alport syndrome
b. chronic glomerulonephritis
c. diabetic nephropathy

A

diabetic nephropathy (kimmelstiel wilson disease)

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16
Q

damage in renal tubular cells caused by ischemic or toxic agents

a. acute tubular necrosis
b. fanconi syndrome
c. diabetes insipidus

A

acute tubular neccrosis

17
Q

this disorders has a odorless urine

a. diabetes insipidus
b. acute tubular necrosis
c. cystitis

A

acute tubular necrosis

Findings: 
  rte cells
  rte casts
  odorless urine
  isosthernuria
hyaline granular waxy and broad cast
18
Q

(+) granular dirty brown cast

a. chronic pyelonephritis
b. cytitis
b. ATN

A

acute tubular necrosis

19
Q

(+) phosphaturia

a. diabetic insipidus
b. fanconi syndrome
c. nephrotic syndrome

A

fanconi syndrome

20
Q

failure of the hypothalamus to produce ADH

a. nephrotic syndrome
b. neurogenic D.I
c. nephrogenic D.I

A

neurogenic Diabetes insipidus

21
Q

low in specific gravity

polyuria

a. cystitis
b. ATN
c, diabetic insipidus

A

diabetic insipidus

22
Q

normal to increase ADH

a. neurogenic D.I
b. nephrogenic D.I

A

nephrogenic D. I

23
Q

normal blood glucose
increase in urine glucose

a. diabetic insipidus
b. renal glycosuria
c. acute interstitial nephritis

A

renal glycosuria

24
Q

ascending bacterial infection in urinary bladder

a. cystitis
b. acute pyelonephritis
c. chronic pyelonephritits

A

cystitis ( lower uti)

25
reflux of urine from the bladder ( vesicourectal reflux) a. cystitis b. acute pyelonephritis c. chronic pyelonephritits
acute pyelonephritis
26
allergic inflammation of the renal interstitium in response to medication a. acute tubular necrosis b. acute interstitial nephritis c. chronic pyelonephritis
AIN
27
increase in eosinophil a. acute tubular necrosis b. acute interstitial nephritis c. chronic pyelonephritis
AIN
28
hematuria, proteinuria, wbc, wbc casts, no bacteria a. acute tubular necrosis b. acute interstitial nephritis c. chronic pyelonephritis
AIN