NEPHROLOGY Flashcards

1
Q

What is seen on EM for Minimal change disease?

A

Fusion of podocytes
Effacement of foot processes

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2
Q

What are the features of minimal change disease?

A
  • Nephrotic syndrome 2ndry to low albumin
  • Normotension
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3
Q

What is the most common renal manifestation of SLE?

A

Diffuse profilerative glomerulonephritis

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4
Q

What are the findings on renal biopsy in Diffuse proliferative glomerulonephritis?

A

Wire loop appearance - endothelial and mesangial proliferation
Immune complex deposition

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5
Q

What are the findings on EM in diffuse proliferative glomerulonephritis?

A

Subendothelial immune complex deposits

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6
Q

What is the MoA of Tolvaptan?

A

Vasopressin V2 receptor antagonist
Rx for ADPKD

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7
Q

Which chromosome is the ADPKD 1 located on?

A

Chromosome 16

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8
Q

Which chromosome is the ADPKD 2 located on?

A

Chromosome 4

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9
Q

What is the triad of Haemolytic Uraemic Syndrome?

A
  • AKI
  • Microangiopathic haemolytic anaemia
  • Thrombocytopenia
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10
Q

What are the causes of secondary HUS?

A
  • E.coli - most common cause in children
  • Pneumococcal infection
  • HIV
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11
Q

What are the blood film findings in HUS?

A
  • Schistocytes
  • Thrombocytopenia
  • Anaemia
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12
Q

What is the MoA of Eculizumab?

A

C5 inhibitor monoclonal antibody

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13
Q

What medication is given to prevent calcium renal stones?

A

Thiazide diurectics - Increases Ca reabsorption

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14
Q

What medication is given to prevent Oxalate stones?

A
  • Cholestyramine - reduces urinary oxlate excretion
  • Pyridoxine
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15
Q

What medication is given to prevent uric acid stones?

A

Allopurinol

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16
Q

What is the MoA of MMF?

A

Blocks purine synthesis –> inhibits proliferation of B and T cells

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17
Q

How does alcohol cause polyuria?

A

ADH suppression in the posterior pituitary –> reduced aquaporin insertion –> reduced water reabsorption

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18
Q

What are the features of nephritic syndrome?

A
  • Haematuria
    Proteinuria
    HTN
    Oligouria
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19
Q

What are the causes of rapidly progressive glomerulonephritis?

A
  • Goodpasture’s syndrome
  • Wegener’s granulomatosis
  • SLE
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20
Q

What are the findings on renal biopsy in progressive glomerulonephritis?

A

Crescenteric glomerulonephritis

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21
Q

Alports syndrome is due to a defect in which collagen type?

A

Type 4 - defect resulting in abnormal GBM

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22
Q

What is seen on renal biopsy in Alports syndrome?

A

Splitting of the lamina densa - basket weave appearance

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23
Q

What are the features of Alport’s syndrome?

A
  • Microscopic haematuria
  • Renal failure
  • B/l sensorineural deafness
  • lenticonus - protrusion of lens
  • retinitis pigmentosa
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24
Q

How does Lithium cause nephrogenic diabetes insipidus?

A

lithium desensitizes the kidney’s ability to respond to ADH in the collecting ducts

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25
What is the MoA of Bicalutamide?
Androgen receptor blocker
26
Which antibody mediates hyperacute rejection?
IgG
27
What type of hypersensitivity reaction is Hyperacute rejection?
Type II
28
What are the features of acute graft failure?
* Rising creatine * Pyuria * Proteinuria
29
Which part of the renal tubule is affected in Fanconi syndrome?
Proximal convuluted tubule
30
What is seen on renal biopsy in membranous glomerulonephritis?
* Spike and dome appearance * Thickened basement membrane with subepithelial electron dense deposits
31
Which antibodies cause membranous glomerulonephritis?
Antiphospholipase A2
32
What are the causes of membranous glomerulonephritis?
* Idiopathic: antiphospholipase A2 * Infection: Malaria, syphillis, Hep B * Malignancy: Prostate, Lung, Lymphoma, Leukemia * Drugs: Gold,penicillamine, NSAIDs * SLE, RA
33
What is the management of membranous glomerulonephritis?
* ACE i * Steroids
34
What causes high plasma aldosterone/renin ratio?
Renal artery stenosis
35
What causes low plasma aldosterone/renin ratio?
Liddle's syndrome (L for Low)
36
What causes high aldosterone and low renin ratio?
Primary hyperaldosteronism
37
What causes raised PSA levels?
* BPH * Prostatitis/UTI * Ejaculation * Vigrous exercise * Urinary retention * Instrumentation of the urinary tract
38
What are the features of Goodpasture's syndrome (Anti - GBM disease)?
* Pulmonary haemorrhage * Rapidly progressive glomerulonephritis
39
What causes anti-GBM disease?
anti-GBM antibodies against Type IV collagen
40
Which HLA is associated with Goodpastures?
HLA DR 2
41
What are the renal biopsy findings in anti-GBM disease?
Linear IgG deposits along the basement membrane **(remember Gs) **
42
What is the management of anti-GBM disease?
* plasma exchange * steroids * cyclophosphamide
43
What are the causes of normal anion gap acidosis?
FUSEDCARS * Fistula * Ureterogastric conduit * Saline * Endocrine (Addison's, hyper PTH) * Diarrhoea * Carbonic anhydrase inhibitors * Ammonium chloride * Renal tubular acidosis * Spironolactone
44
How does IgA nephropathy (Berger's disease) present?
Macroscopic haematuria post URTI 1-2 days post infection
45
What is seen on renal histology in IgA nephropathy?
Mesangial hypercellularity Positive immunofluorescence for IgA and C3
46
What are staghorn (struvite) stones composed of?
Magnesium ammonium phosphate
47
What is the mode of inheritance in Alport's syndrome?
X-linked dominant
48
What is the MoA of Tamsulosin?
Alpha - 1 antagonist - decreases smooth muscle tone
49
What is the MoA of Finasteride?
5 - alpha reductase inhibitor - blocks conversion of testosterone to DHT
50
What are the complications of nephrotic syndrome?
* VTE - due to loss of antithrombin III * Hyperlipidaemia - increased risk of CVE, ACS * CKD * Hypocalcaemia due to loss of Vit D in urine
51
What cardiac abnormality is associated with ADPKD?
Mitral valve prolapse Aortic root dilation Aortic dissection
52
What is the common cause of nephrotic syndrome in young adults?
Focal segmental glomerulosclerosis
53
What are the causes of focal segmental glomerulosclerosis?
* Idiopathic * IgA nephropathy * HIV * Alports syndrome * Sickle cell
54
What are the findings of FSG on renal biopsy?
Effacement of foot processes
55
What is the management of HIV-associated nephropathy?
Antiretroviral therapy
56
What is the management of renal stones?
* 5-10mm - shockwave lithotripsy * 10-20 - shockwave lithotripsy / ureteroscopy * >20mm percutaneous nephrolithotomy
57
What type of stones are semi-opaque on Xray?
Cysteine stones
58
Which stones are radio-lucent?
Urate and xanthine stones
59
What are the features of Acute Interstitial nephritis?
Fever, rash, arthralgia Eosinophilia Mild renal impairment HTN
60
What is seen on urine microscopy in Acute interstitial nephritis?
Sterile pyuria White cell casts
61
Which drugs commonly cause Acute Interstitial nephritis?
Penicillin Rifampicin Antibiotics Furosemide NSAIDs Allopurinol
62
Which systemic diseases cause Acute Interstitial nephritis?
SLE Sarcoidosis Sjogren's
63
What is reabsorbed in the PCT?
Sodium, glucose and amino acids
64