Nephro/GU Flashcards

1
Q

An 18 month old girl has periorbital swelling. Her albumin is 26. Her urine is negative for protein. What do you do for diagnosis?

a) Serum trypsin
b) Stool alpha anti-trypsin
c) Urine creatinine excretion
d) ECHO

A

b) Stool alpha anti-trypsin

Other potential causes of hypoalbuminemia include liver disease (reduced production) and inadequate protein intake. Very rarely hypoalbuminemia can result from an extensive skin disorder causing protein loss via the skin. Measurement of stool α1-antitrypsin is a useful screening test for protein-losing enteropathy.

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2
Q

What is important to know in order to determine if BP is within normal range?

a) Weight
b) Ethnicity
c) Height
d) Age

A

age, sex, and height percentile.

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3
Q

11 year old boy who has never been dry at night. Father had nocturnal enuresis until age 10. Having difficulty and not able to spend time at his friends’ houses for sleepovers. What is the best advice regarding management?

a. Alarm
b. Imipramine
c. DDAVP
d. Oxybutynin

A

DDAVP
Synthetic analogue of ADH. Not curative. Desmopressin acetate’s greatest value may be for short-term treatment, in settings such as camp or sleepovers, rather than as an attempt at a cure

Alarm - Alarm therapy requires a commitment from parents and other siblings because the alarms are sufficiently loud that often all members of the household are wakened when the alarm goes off. Alarms are impractical for ‘sleepovers’ and camp.

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4
Q
A child is receiving high dose prednisone for nephrotic syndrome. He is due for his DPTP-Hib. When can you give it?
Today
1 month
6 months
11 months
A

today
NON LIVE
Inactivated vaccines and toxoids can be administered to all immunocompromised patients in usual doses and schedules, although the response to these vaccines may be suboptimal.

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5
Q

16 year old girl comes to your office. Her BMI is 27 and she has stage 1 hypertension. No protein present on urinalysis. What is the next step in managing her high blood pressure?

1) Beta blocker
2) Calcium channel blocker
3) Lifestyle
4) ACEi

A

lifestyle
The mainstay of therapy for children with asymptomatic mild hypertension without evidence of target-organ damage is therapeutic lifestyle modification with dietary changes and regular exercise. Weight loss is the primary therapy in obesity-related hypertension.

Indications for pharmacologic therapy include symptomatic hypertension, secondary hypertension, hypertensive target organ damage, diabetes (types 1 and 2), and persistent hypertension and STAGE 2 HTN (>99th) -despite nonpharmacologic measures.

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6
Q

Which of the following is seen in distal RTA?

a. Hyperkalemia
b. Hyponatremia
c. Hypophosphatemia
d. Hypercalciuria

A

d. Hypercalciuria
can also get hypokalemia
Renal tubular acidosis is characterized by non-anion gap (hyperchloremic) metabolic acidosis in the setting of normal GFR. There are 4 types:
Type I - classic distal RTA- cant secrete H
Type II - proximal RTA - cant absorb bicarb
Type III - combined proximal and distal
Type IV - hyperkalemic RTA

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7
Q

Most common renal stone in children

a) Calcium oxalate
b) Cystine
c) Urate
d) Struvite

A

calc oxalate

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8
Q

4 year old girl with glomerulonephritis, hypertension, and vomiting x3 days. Most probable test to determine diagnosis

a) C3
b) Renal Biopsy

A

C3
GN with Low C3:
Systemic diseases: Lupus nephritis, subacute bacterial endocarditis, shunt nephritis, essential mixed cryoglobulinemia, visceral abscess
Renal disease: Acute post-infectious GN, membranoproliferative GN type I

GN with Normal C3
Systemic diseases: Polyarteritis nodosa, hypersensitivity vasculitis, granulomatosis with polyangitis, HSP, goodpasture
Renal: IgA nephropathy, idiopathic rapidly progressive GN (type I - anti GBM, type II - immune complex, type III - pauciimmune), postinfectious GN (non-strep)

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9
Q

15 yo with 3+ proteinuria.

a) Check Protein twice each am

A

check three times in a row

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10
Q

What is the result when you have a diagnosis of central DI post water deprivation test?

a) Decreased Urine osmolality
b) Increased urine osmolality
c) Decreaed Serum osmolality
d) Increased serum osmolality

A

increased serum osmolality

and urine will stay LOW as u keep spilling water

with ADH deficiency, high serum osmolality and low urine osmolality

this just diagnosis DI- next step give DDAVP to determine central vs peripheral

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11
Q

Boy with enuresis, what is a good non pharm way to treat it

a) Positive reinforcement
b) Bed Alarm
c) Ddavp
d) Bladder training

A

bed alarm

DO not reward them

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12
Q

Children with turners have which renal abnormality at rates higher than healthy population?
a -horseshoe kidney
b -MCDK
c -Vesicoureteral reflux

A

A horseshoe kidney

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13
Q

What glomerular disease is associated with a low C3?

          	a. Membranous nephropathy
          	b. Alports
          	c. IgA nephropathy
          	d. Membranoproliferative glomerulonephritis
A

MPGN
GN with Normal C3
Systemic diseases: Polyarteritis nodosa, hypersensitivity vasculitis, granulomatosis with polyangitis, HSP, goodpasture, Alports (hematuria, sensorineural hearing loss)
Renal: IgA nephropathy, idiopathic rapidly progressive GN (type I - anti GBM, type II - immune complex, type III - pauciimmune), postinfectious GN (non-strep)

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14
Q

A child presents with hypertension, urine dip shows blood and protein, creatinine and urea are elevated, C3 and C4 are normal. What is the most likely diagnosis?

a. SLE
b. Membranoproliferative glomerulonephritis
c. Post-infectious glomerulonephritis
d. IgA nephropathy

A

d. IgA nephropathy

LOW C3- SLE, MPGN, Post infectios

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15
Q
4 year old child with nephrotic syndrome on steroids. Presents with a swollen and tender abdomen. Looks septic. What test would give you the diagnostic:
a. Paracentesis
b. CT scan
c. MRI
D. Laparotomy
A

parecentesis

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16
Q

Child with distal RTA who doesn’t take his meds. 2 months after last visit, presents with bilateral leg weakness and doesn’t want to walk. What does he have?

a. Chronic acidosis
b. Hypokalemia
c. Hypocalcemia
d. Hypomagnesemia

A

hypokalemia - gives bilat weakness

severe metabolic acidosis, urine pH cannot be reduced < 5.5, hyperchloremia (because of loss of HCO3-), hypokalemia (because of inability to secrete H+), hypercalciuria, hypocitraturia (chronic metabolic acidosis leads to impaired urinary citrate excretion, which worsens hypercalciuria)

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17
Q

7 y.o boy presents with left-sided night time flank pain. An US reveals left-sided hydronephrosis. what do you do next?

a. VCUG
b. Nuclear scan with lasix washout
c. DMSA scan
d. CT abdomen with contrast

A

nuclear scan with lasix washout

MAG-3 administered with lasix - looks at differential renal function to assess for obstruction

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18
Q

chool aged child with pH 7.15, HCO3 9, Na 138, Cl 121, PO4 0.7, K 3.0. Also has urine pH of 5 and glucose in urine. What do you check? Which test is most likely to reveal the diagnosis?

a. Leukocyte for cystine
b. Urine ca/cr ratio

A

leukocyte for cysteine

metabolic acidosis, non-aniongap
either RTA or diarrhea
distal RTA DO NOT have acidic urine.

RTA with pH <5.5, glucosuria = proximal RTA
Proximal RTA almost always = fanconi
Most common cause of fanconi = cystinosis

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19
Q

RTA proximal vs distal

A

proximal - acidic urine,
distal
pRTA presents with polyuria, dehydration, anorexia, vomiting, constipation, hypotonia and FTT in first year of life. Non-anion gap metabolic acidosis, normal urinalysis (except in Fanconi), urine pH < 5.5 because distal acidification mechanisms are intact, +/- renal failure.

severe metabolic acidosis, urine pH cannot be reduced < 5.5, hyperchloremia (because of loss of HCO3-), hypokalemia (because of inability to secrete H+), hypercalciuria, hypocitraturia (chronic metabolic acidosis leads to impaired urinary citrate excretion, which worsens hypercalciuria)

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20
Q

You are asked to assess a 10 day old baby with weak abdominal muscles and cryptorchidism. The baby is also found to have bilateral flank masses. What is the most likely association with this picture to explain the flank masses?

a. polycystic kidneys
b. multicytic dysplastic kidneys
c. hydronephrosis
d. bilateral wilms tumors

A

hydronephrosis

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21
Q

Shows picture of genitalia (looks labial adhesions) in an 18mo girl. What to do?

Estrogen cream to the affected area

b. Abdo US
c. Call CAS
d. Refer to urology

A

estrogen cream to affect area

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22
Q

6 yr American African girl presented with blood in underwear. She has some trouble urinating, no fever, no other symptoms. On exam there is a red mass coming out of vagina..

a. Urethral prolapse
b. Cancer

A

black + blood spotting
it is URETHRAL PROLAPSE
and give estrogen cream 2-3 times daily

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23
Q

Patient presents with edema, abdominal distension, and proteinuria. Patient also has fever and is found to have spontaneous bacterial peritonitis. What is the MOST likely pathogen causing the SBP.

a. Steptococcal pneumoniae
b. E. Coli
c. Enterococcus
d. Listeria

A

strep pneumo

e coli #2

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24
Q

Patient with history of sore throat. Urine shows microscopic hematuria. What is the natural course?

a. It will resolve over time
b. Progress to chronic renal disease
c. microscopic hematuria
d. proteinuria and hypertension

A

resolve over time

Progress to chronic renal disease - very rare

c. microscopic hematuria - can last up to a year
d. proteinuria and hypertension - in acute phase

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25
Q

Antenatal diagnosis of hydronephrosis. What to do before d/c?

a. VCUG
b. MAG scan
c. Ultrasound

A

ultrasound at 48 hours

if persistent then VCUG and nephro referal

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26
Q

A 14 year old boy presents with an acutely painful scrotum. You suspect testicular torsion. Which of the following is true?

a. absence of the cremasteric reflex is common
b. blue discoloration of the scrotum is pathognomonic
c. you have 36 hours to treat before losing the testes

A

absence of crem reflex ommon

non viable after 24 hours

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27
Q

he reason we do orchidopexy?
a. reduce the chance of testicular cancer
b. allow better testicular examination
c. increase fertility potential - JELD says best as per their lecture
ALL technically correct

A

increase fertility

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28
Q

A 10 month old boy comes to ER. Acute onset of scrotal swelling. Parents have noted on and off swelling in the past few days. Today a bit irritable. VSS stable. On exam, swollen scrotum, does not reduce; transilluminates well, testicle palpable separately. Likely diagnosis?

a. epididmytis
b. testicular torsion
c. acute hydrocele
d. incarcerated hernia

A

acute hydrocele

not super upset

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29
Q

Smooth, firm, tubular mass in scrotum that transilluminates, not febrile, irritable for a week. Discomfort with examination, testes palpable and are distinct from this mass. Not reducible, no vomiting.

a. incarcerated inguinal hernia
b. acute non-communicating hydrocoele
c. epididymitis
d. testicular torsion

A

acute non-communicating hydrocoele

as it transilluminates

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30
Q

3 mo baby boy with right inguinal mass. Anorexia and irritabiliy x 3days. Mass transilluminates, soft and separate from testes. Diagnosis:

a. acute non-communicating hydrocele
b. incarcerated inguinal hernia
c. Tumor
d. torsion of testes

A

INCARCERATED INGUINAL HERIA - could also be hydrocele

tunica vaginalis communicates, maybe they have hydrocele and inguinal hernia

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31
Q

Which of the following is important in measuring blood pressure:

a. height
b. weight
c. Tanner stage

A

height

BP varies with age, sex, and height in children

ABPM uses a portable automated device that records blood pressure (BP) over a specific time period (usually 24 hours).

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32
Q

Kid with hypertension confirmed by ambulatory blood pressure monitoring. Has BP 121/86. What do you do?

a. start him on captopril
b. observe and repeat an ambulatory blood pressure test
c. renal ultrasound

A

renal u/s

ABPM if positive over 24 hours that is diagnostic

if its by visits 3x
consider starting amlodipine

DONT do ace inhibitor/pril - with renal artery stenosis, causes hyperK, aki, and inc cr

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33
Q

Periorbital swelling with no tenderness, no fever and normal blood pressure. What do you do?

a. reassure
b. check for proteinuria
c. start antibiotics

A

check for proteinuria

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34
Q

tests for hypertension?

A

RENAL lytes and renal function
uurinalysis, renal ultrasound

HEART fasting glu and lipids

END ORGAN echo, acr, retinal exam

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35
Q

Periorbital swelling with no tenderness, no fever and normal blood pressure. What do you do?

a. reassure
b. check for proteinuria
c. start antibiotics

A

check proteinuria

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36
Q

Which of the following is a presentation of HUS?

a. Coombs + anemia
b. Thrombocytopenia
c. Myoglobinuria

A

thromboycypeona

Characterized by the triad of microangiopathic hemolytic anemia, thrombocytopenia and renal insufficiency.
2 major categories of disease:
Infection associated (E. coli O157:H7, Shigella dysenteriae type 1, HIV, neuraminidase producing Strep pneumo)
Genetic (atypical HUS)

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37
Q

Recurrent hematuria in a young male with a speech delay

a. IgA nephropathy (usu occurs within 2 days of getting ill)
b. Alport syndrome
c. PSGN
d. MPGN

A

alport

hematuria
often associated with sensorineural hearing loss and ocular abnormalities
C3 normal
xlinked

IF a GIRL - consider IgA nephropathy

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38
Q

6 y.o. girl with a history of bilateral VUR and recurrent UTIs, including two febrile illnesses. Has been off antibiotics and infection-free for two years. Repeat u/s and VCUG show normal kidneys, but grade 1-2 reflux bilaterally. What do you recommend:

a. consider operative repair
b. repeat cystogram every 2 years
c. restart prophylactic antibiotics
d. continue non-interventional observation

A

continue non-interventional observation

if put on abx, reasses 3-6 mo

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39
Q

12y old with diabetes Type I since the age of 5 with microalbuminuria despite optimum control of his diabetes. What should you start him on :

a. hydrochlorothiazide
b. nifidepine
c. enalapril

A

enalapril

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40
Q

Diabetic with microalbuminuria. What would you prescribe?

a. Enalapril
b. Hydrochlorothiazide
c. Nifedipine
d. Salt and water restriction

A

enalapril

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41
Q

14 year old boy in office for pre-camp physical, 3+ protein in urine x2, exam is normal, what is most likely cause?

a. exercise induced -
b. IgA nephropathy -
c. nephritic syndrome -
d. Orthostatic

A

a. exercise induced - also possible but less common
b. IgA nephropathy - persistent microscopic hematuria more common
c. nephritic syndrome - would have other symptoms
d. Orthostatic

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42
Q

Patient to ER with following labs: Na 135, K 2.3, Cl 116, Bicarb 9, pH 7.14, most likely cause?

a. RTA
b. DKA
c. lactic acidosis
d. Vomiting

A

RTA
Non- anion gap metabolic acidosis, hypokalemia, normal sodium, hyperchloremia
Anion gap = Na - HCO3 - Cl = 10 (normal)
RTA: RTA is a disease state characterized by a normal anion gap (hyperchloremic) metabolic acidosis

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43
Q

RTA 1

A

DISTAL
Impaired distal acid secretion
Severe metabolic acidosis with high urine pH (>5.5)
Loss of bicarb → hyperchloremia
Hypokalemia from inability to secrete H+
Hypercalciuria + nephrocalcinosis usually present

44
Q

RTA 2

A

PROX
Impaired proximal bicarbonate reabsorption
Usually occurs as part of global proximal tubular dysfunction or Fanconi syndrome
Non-anion gap hyperchloremic metabolic acidosis
Urine pH <5.5 because distal H+ secretion intact
Glucosuria, aminoaciduria, phosphaturia
Hypophosphatemia (can cause rickets), hypokalemia
Patients can have FTT, polyuria, anorexia, vomiting, constipation

45
Q

A child with recent Group A strep infection, normal C3, C4, slightly increased creatinine, Platelets and low hemoglobin, with blood in the urine

a. HSP -
b. HUS -
c. Post strep GN -
d. IgA nephropathy -

A

HUS
usu caused by strep pneumo

NOT GAS

a. HSP - need other sx to make diagnosis
b. HUS - if they meant both Plts and Hgb low, but no diarrhea?
c. Post strep GN - C3 would be low
d. IgA nephropathy - possible, but no anemia usually

46
Q

Teenager found to have struvite stone. What would be next investigation?

a. Urine calcium/Po4
b. Urine culture
c. 24 hour urine ca

A

urine culture

klebsiella
ecoli and pseudomonas

47
Q
  1. Asymptomatic renal cyst 2 cm
A

monitor

48
Q

Distal RTA (type 1), what is the electrolyte abnormality?

a. Glycosuria -
b. Hypercalciuria
c. Increased anion gap

A

HYPERCALCURIA

a. Glycosuria - this is proximal RTA w/ Fanconi syndrome
b. Hypercalciuria
c. Increased anion gap acidosis - anion gap is normal

49
Q

7 year old girl with BP 140/80 with sx of ?PSGN & no signs given in history of end-organ damage. Management?

a. IV labetolol
b. PO nifedipine
c. Salt/H2O restriction

A

salt h20 restrict

50
Q

Which is a factor in determining what a child’s mean BP should be:

a. Height
b. Weight
c. Tanner stage
d. Ethnicity

A

height

age, sex and height.

51
Q

6 yo female with prior history of recurrent UTI, 2 of them afebrile, known bilateral reflux. Last VCUG shows ongoing low grade reflux. She has been off antibiotics and infection free for 2 years. What to do next?

a. Restart antibiotics
b. Observe only
c. VCUG every 2 years

A

observe

52
Q

15 yo female with 2+ protein on routine exam. What to do?

a. 24 hr urine protein
b. first morning urine analysis x 2
c. Renal function tests

A

FIRST MORRNING URINE X2

53
Q

11 year old girl with gross hematuria. She has a history of 3 prior episodes, all associated with upper respiratory infections. Her gross hematuria resolves in one day, but she continues to dip positive for microscopic hematuria. What test would give you the diagnosis?

a. C3, C4
b. ASOT
c. Immunoglobulins

A

C3 AND C4

if normal then it would be IgA

54
Q
6mm pelicalviceal dilatation noted on antenatal and postnatal u/s. What should be done next?
start prophylactic antibiotics
 VCUG
DMSA
repeat U/S in 2 months
A

rpt in 2 mo

likely uou would do nothing

55
Q

Description of testicular torsion. How can this diagnosis be confirmed?

a. testicular ultrasound
b. nuclear scan

A

testicular u/s

56
Q

What is the most common etiology of hypertension in adolescents?

a. essential hypertension
b. renal artery stenosis
c. congenital renal disease
d. coarctation of the aorta

A

essential

57
Q

5 day old infant in nursery has low urine output. Creatinine is 120. Renal ultrasound shows absent left kidney. The right kidney is at the low end of normal for size, and has consistent/uniform echodensity throughout. Which of the following is most likely?

a. Prognosis depends on liver and lung status
b. Likely will progress to end stage renal disease in childhood
c. Likely will progress to end stage renal disease in mid adulthood
d. He will have normal renal function

A

likely progress to ESRD

When one kidney absent/nonfunctioning, other should compensate by hypertrophy. The fact that this one is normal for size and already showing signs of renal failure (ie low U/O, high Cr) would think he will progress to ESRD -

58
Q

3 month old boy with UTI and grade 2 VUR on Right side. Which is the most clinically relevant way to detect renal scarring.

a. IV pyelography
b. nuclear renal scan (MAG or DMSA)
c. Renal excretion scan (DTPA)
d. VCUG

A

MAG nuclear renal scan

59
Q

All of the following about Alport’s are true except:

a. Girls have worse prognosis
b. Bad prognosis is with gross hematuria in childhood
c. Progressive sensorineural hearing loss in childhood
d. 15% have end stage renal disease before age 15
e. 2-3% of all end stage renal disease is due to Alport’s

A

girls have worst prognosis

60
Q

7 year old with microscopic hematuria most likely dx?

a. IgA nephropathy
b. alports
c. idiopathic

A

idiopathic

61
Q

Child with HUS following E coli enteritis, admitted in renal failure. How do you treat/screen her two siblings who are having bloody diarrhea?

a. admit them, do CBC, BUN/Cr, start antibiotics
b. do CBC, BUN/Cr, follow them clinically
c. do CBC, BUN/Cr, start antibiotics
d. do nothing unless they develop signs or symptoms of HUS

A

b. do CBC, BUN/Cr, follow them clinically

abx not recommended

62
Q

What is true about primary nephrogenic DI

a. female predominance
b. mental retardation
c. growth deficiency

A
growth def
are cause of DI
defect in receptors for ADH - so resistant to ADH - AVPR2 gene
gene for receptors is X linked - so more likely in males
present with: 
massive polyuria (very wet diapers)
volume depletion
hyperNatremia
hyperthermia
irritability
crying
constipation
poor weight gain
multiple episodes of hypernatremic dehydration causes developmental delay and mental retardation
63
Q

A child with multicystic dysplastic kidney. What is the likely association?

a. severe hypertension
b. vesico-uretero reflux
c. cataracts
d. brain aneurysm

A

VUR

Contralateral hydronephrosis is present in 5-10% and 15% have contralateral VUR, of patients with MCDK

64
Q

Previously well 10yo boy presents with microscopic hematuria. Renal ultrasound reveals 1 cm stone in pelvic basin. Likely:

a. oxaluria
b. idiopathic hypercalciuria
c. aminoaciduria
d. cystinuria

A

idiopathic hypercalciuria is most common cause of stones
most common metabolic urine abnormality found in kids:
Hypercalciuria, 50 %
Hyperoxaluria, 10 to 20 %
Hyperuricosuria, 2 to 8 %
Cystinuria, 5 %
Hypocitraturia, 10 %
Most urinary calculi are either calcium oxalate and/or calcium phosphate.

65
Q

What is the management of 10 yo male with nocturnal enuresis (normal u/a)?

a. conditioning alarm
b. DDAVP
c. TCA
d. diapers

A

conditioning alarm

66
Q

In SIADH you DO NOT have:

a. serum hypouricemia
b. urine hyperkalemia
c. high urine sodium excretion
d. urine/serum osm ratio >1.5

A

urine hyperkalemia

urine/serum osm ratio >1.5 - expect really low serum osm with high ADH

67
Q

Patient with HSP. What would you monitor

a. urinalysis
b. IgA
c. stool for O/P
d. AXR

A

urinalysis

68
Q

What condition is not associated with low complement levels?

a. MPGN
b. HSP
c. Shunt nephritis
d. Lupus nephritis
e. Post strep GN

A

HSP -

shunt and lupus causes secondary MPGN

Low complement GN:
Systemic: SLE, endocarditis, cryoglobulinemia, shunt nephritis
Isolated renal: post-infectious GN, MPGN

Normal complement GN:
Systemic: HSP, ANCA-associted (Wegener’s, PAN), Goodpasture’s syndrome, hypersensitivity vasculitis
Isolated renal: IgA nephropathy, anti-GBM disease, RPGN

69
Q

51/2 boy with recent URTI, now has respiratory distress and BP150/110, most likely

a. anxiety
b. pneumonia
c. Henoch-schonlein purpura
d. post strep GN

A

post strep GN

70
Q

11y old presents with a 4 day hx of tea colored urine. He had an upper respiratory tract infection 10 days ago. There is no hx of urgency or dysuria. Normal PE. Blood pressure 110/75 (not hypertensive). Urine analysis: red blood cells, 0-2 WBC and 1+ protein.

a. cystitis
b. Hypercalcuria
c. IGA nephropathy
d. Post infectious GN

A

post infectious GN

nephritis
proteinrua
Hemuatira
Azotemia
Renal inusff
Oliguria
HTN

ystitis - ?could they mean hemorrhagic cystitis, could be secondary to adenovirus, should present with LUTS.

b. Hypercalcuria - idiopathic hypercalciuria can cause gross hematuria, should have pain, LUTS, diagnosed by 24 hour urine calcium excretion > 4mg/kg, spot calcium/creatinine ratio.
c. IGA nephropathy - shorter latency period, should be 1-2 days after URTI, M>F
d. Post infectious GN - would be helpful to distinguish from IgA nephropathy if C3 levels were given. Low C3 in post infectious GN and normal C4 in IgA nephropathy.

71
Q

A 17 y adolescent male complains of several weeks of swelling above his left testicle. He does not have any pain in the area. He is sexually active and states that he uses condoms. On PE: he has a mass along the spermatic cord that feels like a bag of worms. Which of the following is the most effective management?

a. ceftriaxone and doxycyclin po
b. Doppler flow studies of testis
c. Radionucleide scan of testis
d. reassurance and education only at that time

A

reassurance and education only at that time

ultrasound - only if R side to r/o abdo mass

72
Q

During the first year of infant’s life, which of the following remains essentially unchanged?

a. GFR
b. nephron number
c. renal blood flow
d. Ability to concentrate urine

A

nephron #

73
Q

5 yo male with fever and rhinorrhea presents with gross hematuria one day later. He has had a previous similar episode 3 months ago. What is the most likely diagnosis?

a. chronic glomerulonephritis
b. post-Strep GN
c. postinfectious GN
d. IgA nephropathy
e. nephrotic syndrome

A

IgA nephropty

74
Q

14 mos male with FTT and vomiting, labs pH 7.31, bicarb 17, K3.5, Na 140, Cl 118, and urine pH 6.3.

a. distal RTA
b. Bartter’s syndrome
c. organic acidopathy
d. nutritional deprivation

A

distal RTA

Renal tubular acidosis = non-anion gap hyperchloremic metabolic acidosis
if urine pH >5.5 + potassium is NOT high = type 1 RTA; distal RTA

Bartter syndrome = hypochloremic metabolic alkalosis
Organic acidopathy = anion-gap metabolic acidosis

75
Q

A newborn infant has a left sided abdominal mass. A renal ultrasound demonstrates multicystic kidney disease. Which of following would this be associated with:

a. ipsilateral hydroureter
b. posterior urethral valves
c. sensorineural hearing loss
d. cataracts
e. risk of malignancy

A

risk of malignancy for life

The risk of associated hypertension is 0.2-1.2%, and the risk of Wilms tumor arising from an MCDK is approximately 1 in 1,200. Because neoplasms arise from the stromal rather than the cystic component, even if the cysts regress completely, the likelihood that the kidney could develop a neoplasm is not altered.

you get CONTRAlateral hydroureter

76
Q

Which of the following is associated with a low C3:

a. Alport’s syndrome
b. nephrotic syndrome
c. post-streptococcal glomerulonephritis
d. hemolytic uremic syndrome
e. Henoch-Schonlein purpura -

A

post strep glomerulopehritis

77
Q

An 8-year-old boy has recurrent episodes of asymptomatic gross hematuria triggered by intercurrent illnesses. Between illnesses, dipstick shows microscopic hematuria. Best test to determine etiology: ***Q

a. immunoglobulins (as per Consensus)
b. C3 and C4 levels (as per Nelson’s)
c. 24-hour urine protein
d. abdominal ultrasound
e. DMSA scan

A

c3 c4

78
Q

6-year-old girl with incidental finding of a 2 cm renal cyst. Appropriate management:

a. observe
b. CT abdomen
c. ultrasound liver
d. urology consult
e. full nephrologic workup

A

observe
Isolated renal cysts are commonly observed within the general population, and the prevalence rises with increasing age.
For both affected adults and children, the principle clinical concern is accurately distinguishing simple renal cysts from complex renal cysts that are associated with malignancy.
if complex CT

79
Q

A 6-year-old child has hypertension and persistent hypokalemia. Most likely diagnosis:

a. hyperaldosteronism
b. Bartter syndrome
c. Addison’s disease
d. renal vein thrombosis
e. aortic coarctation

A

hyperaldosterosnims

Primary hyperaldosteronism:
excessive aldosterone secretion causes hypertension, hypokalemia. Also high Na, low Cl, low Mg. Urine is neutral or alkaline. High urine potassium

Aortic coarctation = hypertension, without hypokalemia
Addison’s disease = hypocortisolism, hypoaldosteronism = hyperkalemia, hypotension
Renal vein thrombosis = hypertension, without hypokalemia
Bartter syndrome = hypotension, metabolic alkalosis, hypokalemia

80
Q

Child presents with failure to thrive, polydipsia, polyuria, and hypokalemic metabolic alkalosis.

a. hyperaldosteronism
b. Bartter syndrome
c. cystinosis
d. renal tubular acidosis
e. congenital adrenal hyperplasia

A

Bartter syndrome - like being on lasix all the time
hypokalemic hypochloremic metabolic akalosis with hypercalciuria, salt wasting
can manifest antenatally, perinatally, in infancy, or in childhood with FTT and history of recurrent dehydration

type4 is HYPOaldosteronisn

81
Q

5½-year-old child with a recent upper respiratory tract infection, now has respiratory distress and BP 150/110. Most likely:

a. anxiety
b. pneumonia
c. myocarditis
d. Henoch-Schonlein purpura
e. post-streptococcal glomerulonephriti

A

post strep glomeuerlonephritis

pulm edema cause resp distress

82
Q

The following are shared by cystinosis and renal tubular acidosis (distal) EXCEPT:

a. hypokalemia
b. nephrolithiasis
c. concentrating defect
d. aminoaciduria
e. hyperchloremic metabolic acidosis

A

b. aminoaciduria

-The main cause of fanconi syndrome is cystinosis
-Clinical features of proximal renal tubular acidosis (Type 2) include Polyuria, polydipsia and dehydration, Growth failure
Hyperchloremic metabolic acidosis
Hypokalemia

Fanconi syndrome (other features)
Glycosuria
Proteinuria/aminoaciduria
Hyperuricosuria

83
Q

Infant post cardiac surgery with poor urine output. BUN 25, Cr 177, urine (low Na, concentrated)

a. ATN
b. prerenal failure
c. anaesthetic injury to kidney
d. obstructive uropathy
e. renal vein thrombosis

A

pre renal

Urine Na <20 = prerenal
Urine Na >20 = renal

84
Q

In a newborn found to have a multicystic-dysplastic kidney, the following is likely:

a. hematuria
b. hypertension
c. ureteropelvic reflux

A

ureteropelvic reflux

85
Q

Child with nephrotic syndrome admitted with edema. Na=125. Best fluids:

a. D5W/0.2% saline
b. D5W/0.45% saline
c. normal saline
d. 3% saline
e. Nothing

A

Treatment of Nephrotic Syndrome:
· sodium restriction <1500mg daily
· water/fluid restriction

86
Q

An 8 year old female presents with microscopic hematuria. She has no symptoms. The most likely diagnosis is:

a. Alport’s
b. Wilms’ tumour
c. IgA nephropathy
d. nephrocalcinosis
e. post streptococcal glomerulonephritis

A

IgA neprhopathy

87
Q

A child is brought to the emergency department after an MVA. There has been a period with prolonged hypotension/hypovolemia. His urine output is now 0.3 ml/kg/hr. His mother states that he was evaluated for hematuria and proteinuria 1 year ago and was told that the child may have renal disease. What is the best way to detect parenchymal kidney disease:

a. Increased tubular reabsorption of urea
b. Decreased urinary creatinine
c. Urinary sodium <10 mmol/L
d. Fractional excretion of Na <3%
e. IVP

A

urinary sodium <10mmol/L

88
Q

You are assessing a 3 week old infant. The weight is 4 kg, the birth weight was 3.6 kg, the blood pressure is 90/55 (high). The mother states that the infant is feeding well. The labs show:
Na 142 (Normal), K 3.6 (low), Cl 113 (high), Cr normal, pH 7.25 (acidotic), urine pH 5.0. What is the most likely etiology
a. hyperaldosteronism
b. RTA, proximal
c. CF
d. Psychosocial failure to thrive

A

RTA

a. Hyperaldosteronism - should have hypokalemia, hypertension, high urine potassium, metabolic alkalosis due to H excretion (when K leaves too)
b. RTA, proximal - urine with pH < 5.5, non metabolic gap metabolic acidosis + hyperchloremic

c. CF - should have hypochloremic, hyponatremic metabolic alkalosis
d. Psychosocial failure to thrive - gained ~ 20g/day

89
Q

Photograph of Prune Belly Syndrome. Which of the following is a consistent association:

a. Posterior urethral valves
b. Progression to renal failure
c. Sex-linked inheritance
d. Polyhydramnios

A

progression to renal failure
in 50% and ESRD 30%
more common in males

usu oligohydramnios

90
Q

A 14 year old boy has hypertension. He is at the 99th percentile for height and weight. What are the THREE investigations you need to do to assess for effects of his hypertension, and what would you be testing for? (3 points)

A

ECHO - looking for LVH
Fundoscopy - looking for papilledema, retinal changes
ACR (albumin to Cr - renal function

91
Q

A boy with family history of renal stones, presents with 24-48h right flank pain. Passed a 5 mm stone determined to be calcium oxalate. Name 4 dietary interventions you would recommend to decrease the risk of further stones.

A

hydration
low Na diet
Low fat diet
limiting animal diet

92
Q

nephrotic syndrome

what vaccine they should get

A

Because children with nephrotic syndrome are at increased risk for serious complications and potentially death from pneumococcal infection, they should receive 23-valent polysaccharide (PPSV23) pneumococcal vaccine if not previously immunized. Pneumococcal vaccine is effective even in children receiving high doses of steroids and it is not associated with an increased risk of relapse

93
Q

What are four other possible causes of his testicular pain?

A

Epididymitis
Incarcerated inguinal hernia
Scrotal trauma
Orchitis

94
Q

What are 3 reasons to refer to a nephrologist?

A
Failure to respond to steroids
Gross hematuria
Hypertension
Renal insufficiency
<1 year >12 years
95
Q

Child with hemolytic uremic syndrome (you are told it is HUS)
What are the 3 characteristic laboratory features of HUS?

A

Microangiopathic hemolytic anemia
Thrombocytopenia
Renal insufficiency

96
Q

5yo nausea and confuse, then seizue 12 hours post tonsillectomy
labs Na 121
serum osm 260
a) urine osm higher than serum osm

A

SIADH

97
Q

child sick with vomitting and diarrhea
feeding sugar water
Na 108
Cr 95 urea 13

correct to 118/120 over 24 hours
3% correct over 4-6 hours
fluid restric
correct to 135-140 in 24 hurs

A

correct to 118/120 over 24 hours

98
Q

4 mo with FTT
gas 7.24, co2 30, HCO3 16
BW- Na 138, Cl 111, K5, P04 2.1, glu 4

A

RTA

Fanconi causes low p04 (its normal here)

99
Q

Distal RTA

a. hypercalcuria
b. hypokalemia

A

hpyercalcuria

100
Q

child with unilat gr 4 VUR, and has had resistance with 2 abx, what to do next

A

stop prophylaxis

101
Q
7yo M left sided night time flank pain, u/s L sided hydro
whats next
a-vcug
b-nuc scan with lasix washout
c-dmsa scan
d- CT with contrast
A

nuc scan with lasix as this diagnosis obstrcution

102
Q

four intervention decrease stones

A

low salt
high urine
more citrate - lemonade
more pho4 and magneisum

103
Q

14yo recurrent, painless hematuria, best test

a) IgA level
b) C3
c) renal us
d) hearing test

A

IGA level

no pain so not ultrasuond for stone
C3- recurrent so not PIGN
hearing test= males alport

104
Q

12 yo with 2 w fever, artharglia an dmaalgia
well but pale
blood and proitein urine
ESR 50 WBC 5, normal platelet

acute rheumatic fever
SLE
wegeners granulmatosis
JRA

A

SLE

105
Q

12 yo with 2 w fever, artharglia an dmaalgia
well but pale
blood and proitein urine
ESR 50 WBC 5, normal platelet

acute rheumatic fever
SLE
wegeners granulmatosis
JRA

A

SLE

usu pancytopenic

106
Q

3 ft of HUS

A

MAHA
thrombocytpenoa
renal abn

NO abx in HUS, do CBC BUN cr and follow clinically

107
Q

most common cause of htn in newborn

A

renovascular