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
Q

reflux of urine from the bladder ( vesicourectal reflux)

a. cystitis
b. acute pyelonephritis
c. chronic pyelonephritits

A

acute pyelonephritis

26
Q

allergic inflammation of the renal interstitium in response to medication

a. acute tubular necrosis
b. acute interstitial nephritis
c. chronic pyelonephritis

A

AIN

27
Q

increase in eosinophil

a. acute tubular necrosis
b. acute interstitial nephritis
c. chronic pyelonephritis

A

AIN

28
Q

hematuria, proteinuria, wbc, wbc casts, no bacteria

a. acute tubular necrosis
b. acute interstitial nephritis
c. chronic pyelonephritis

A

AIN