Renal Flashcards

1
Q

Alports syndrome inheritance pattern

A

x linked dominant

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2
Q

AKI definition

A

a rise in serum creatinine of 26 micromol/litre or greater within 48 hours
a 50% or greater rise in serum creatinine known or presumed to have occurred within the past 7 days
a fall in urine output to less than 0.5 ml/kg/hour for more than 6 hours in adults and more than

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3
Q

Risk factors for squamous cell carcinoma of bladder

A

Schistosomiasis
Smoking

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4
Q

Risk factors for urothelial (transitional cell) carcinoma of the bladder include:

A

Smoking
most important risk factor in western countries
hazard ratio is around 4
Exposure to aniline dyes
for example working in the printing and textile industry
examples are 2-naphthylamine and benzidine
Rubber manufacture
Cyclophosphamide

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5
Q

three typical features of HUS

A

low HB, thrombocytopenia and renal failure in a child

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6
Q

minimal change biopsy findings

A

renal biopsy
normal glomeruli on light microscopy
electron microscopy shows fusion of podocytes and effacement of foot processes

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7
Q

Beckwith-Wiedemann syndrome

A

inherited condition associated with organomegaly, macroglossia, abdominal wall defects, Wilm’s tumour and neonatal hypoglycaemia.

Wiedemann = wide man = large tongue, organs, kidney tumour

Wilms MOAN(Wilm’s tumor, macroglossia ,organomegaly ,abdominal wall defect ,neonatal hypoglycemi

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8
Q

chromosome for wilms

A

11 (wilms tumour = 11 letters)

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9
Q

normal anion gap and how to calculate

A

8-15

(na + k) - (cl + HCO3)

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10
Q

IgA Nephropathy histology

A

mesangial hypercellularity and positive immunofluorescence for IgA & C3

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11
Q

Post Streptococcal glomerulonephritis histology

A

Subepithelial humps, granular deposits having ‘starry sky appearance

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12
Q

tolvaptan

A

Tolvaptan is recommended in selected cases of APCKD to prevent or slow the progression of renal failure. its a vasopressor 2 agonist

In ADPKD, there is an overproduction of cAMP in the kidneys in response to vasopressin.

The over production of cAMP leads to increased cell growth and division which leads to the cysts forming.

Hence, tolvaptan blocks vasopressin 2 receptors, which prevents the formation of cAMP, which prevents the excessive cell division, which prevents cysts forming.

They will pee alot as a result though.

Maybe can remember it as Tol-Tap-Tan. Cause when you take it, the ‘tap’ keeps on running.

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13
Q

HIV-associated nephropathy (HIVAN) 5 features

A

massive proteinuria resulting in nephrotic syndrome
normal or large kidneys
focal segmental glomerulosclerosis with focal or global capillary collapse on renal biopsy
elevated urea and creatinine
normotension

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14
Q

positive cyanide-nitroprusside test

A

cysteinurria

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15
Q

Antibody associated with idopathic membranous glomerulonephritis

A

Idiopathic membranous glomerulonephritis is related to anti-phospholipase A2 antibodies

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16
Q

Causes of Fanconis syndrome

A

cystinosis (most common cause in children)
Sjogren’s syndrome
multiple myeloma
nephrotic syndrome
Wilson’s disease

Fanconi syndrome describes a generalised reabsorptive disorder of renal tubular transport in the proximal convoluted tubule resulting in:
type 2 (proximal) renal tubular acidosis
polyuria
aminoaciduria
glycosuria
phosphaturia
osteomalacia

17
Q

membranoproliferative glomerulonephritis Which type of complement is likely to be low

A

C3

18
Q

calciphylaxis

A

rare complication of end-stage renal failure. These painful necrotic skin lesions are linked with hypercalcaemia and hyperphosphataemia

Calciphylaxis lesion are intensely painful, purpuric patches with an area of black necrotic tissue that may form bullae, ulcerate, and leave a hard, firm eschar

19
Q

Atypical heamolytic syndrome Mx

A

atypical haemolytic syndrome - if complement-mediated - responds to eculizumab.

20
Q

Acute interstitial nephritis triad

A

AIN is characterised by a triad of rash, fever and e. especially in the setting of arthralgia, sterile pyuria and white cell casts. White cell casts are caused by an acute inflammatory state, either by active infection such as pyelonephritis or an immune nephritic process, which involves cells sloughing in the tubular lumen.osinophilia.

21
Q

most common histological pattern seen in lupus nephritis

A

diffuse proliferative glomerulonephritis.

22
Q

Stag horn calculus is made of?

A

STruvite

23
Q
A