Renal / Urology Flashcards

1
Q

Benign prostatic hyperplasia (BPH) - def? Sx? Ix? Mx?

A

Def: slowly progressive hyperplasia of periurethral (transition) zone of prostate gland –> urinary outflow obstruction

  • Common - occuring primarily in elderly men

Sx: lower urinary tract symptoms (FUND HIPS)

Ix: urinalysis (UTI), PSA (cancer) ± US/CT (abdo/pelvis)/cystoscopy

Mx:

  • Acute retention = CATHETERISE
  • Conservative - watchful waiting
  • Medical:
    • Alpha-blocker (relax sm muscle around prostatic urethra) e.g. tamsulosin
    • 5-alpha-reductase inhibitor (reduce conversion of testosterone –> dihydrotestosterone - reducing androgenic stimulation of prostate) e.g. finasteride
  • Surgical: TURP (transurethral resection of the prostate - shave extra prostate), open prostatectomy
    • NOTE: TURP not curative - will continue to grow
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2
Q

Urinary tract calculi - def? presentation? Stone types? Ix? Mx? When to ADMIT/what to do if managed @home?

A

Def: crystal deposition within the urinary tract

Presentation: severe loin to groin pain (ureteric colic - starts around back and moves towards groin)

Stone types:

  • Ca oxalate (80%)
  • Mg Ammonium Phosphate (struvite) - likely staghorn calculi
    • Associated with proteus mirabilis inf
  • Urate
  • Cysteine

Ix:

  • Bedside - urine dip (microscopic haematuria)
  • Bloods - U&E (post-renal AKI)
  • Imaging - gold standard non-contrast CT KUB (kidneys, ureters, bladder)
    • Contrast is excreted by kidneys - looking for bright white light of Ca –> if you give contrast it will mask the finding

Mx:

  • Infected & obstructed = pyonephrosis –> URGENT decompression via NEPHROSTOMY (or retrograde w/ JJ stent)
    • Opening between kidney & skin w/ nephrostomy bag for external collection
    • Nephro (kidney) stomy (opening)
  • <5mm (on CT) - allow spontaneous passing, retain stone for analysis
  • >5mm (on CT):
    • Ureteroscopic lithotripsy - endoscope into ureter & using mechanical force/laser to destroy stone
      • Uretero (through ureter) scopic (camera) Litho (stone) tripsy (crush)
    • Extracorporeal shockwave lithotripsy - external USS to destroy stone
      • Extra (outside) corporeal (body) shockwave (USS) Lithtripsy (crushing stone)
    • Percutaneous nephrolithotomy - ONLY if stone in kidney (e.g. staghorn calculi), extract stone through skin in back
      • Percutaneous (through skin) Nephro (kidney) lith (stone) otomy (cutting)

When to ADMIT:

  • Pain not controlled
  • Significantly impaired renal function
  • Single kidney
  • Pyrexia/sepsis
  • Stone >5mm

If managed at home:

  • High fluid intake + return if pain worsening/develop temperature
  • OPA in 4 weeks with CT-KUB on arrival –> if stone still present need lithotripsy/nephrolithotomy
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3
Q

Scrotal masses - ddx?

A

DDx:

  • Testicular torsion - EMERGENCY & TIME-URGENT
    • Elevated testis, loss of cremasteric reflex, very tender
    • Tx: bilateral orchidopexy (orchidectomy - if necrotic)
  • Can you feel above swelling?
    • YES - swelling separate from testis?
      • YES - Epididymal cyst OR Varicocele
      • NO - Tender?
        • YES - Epididymo-orchitis (<35 - chalmydia, >35 - E.coli)
        • NO - Hydrocele OR Tumour (raised AFP/b-hCG)
    • NO - Inguinal hernia
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4
Q

Hydrocele - def? Ix?

A

Def: collection of fluid in tunica vaginalis

Ix: US, testicular tumour markers (AFP & bHCG - secreted by tumour, LDH - necrosis), urine culture (inf)

Causes: idiopathic, inf, trauma, tumour

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5
Q

Varicocele - def? What side is more common? What is it associated with x2? How can I reduce swelling?

A

Def: distended veins of pampiniform plexus

Key points:

  • More common on left (the way left testicular vein drains into left renal vein)
  • Assoc w/ infertility, renal cancer
  • Swelling may reduce when lying down
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6
Q

Testicular cancer - Epidemiology & mets? Ix? Mx?

A

Epidemiology & mets:
* Mets to para-aortic LNs
* Most common malignancy in males 20-40yrs

PC: painless mass (30% painful), dragging sensation

Ix:
* Blood testicular tumour markers: alpha-fetoprotein, beta-hCG, LDH (necrosis, others secreted by tumour itself)
* Testicular US –> CT-CAP for staging (would likely do orchidectomy before CT)
* Urine dip (look for infection) –> culture

Mx:
* Orchidectomy – take inguinal approach (scrotal approach risks mets and inguinal is coming out the same way the testicle drops) - only time would not do this first is when respiratory compromise then would do chemo first
* BEP chemotherapy follow-up = very good response typically
* Very good prognosis - good/intermediate prognosis groups have >90% 5-yr survival

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7
Q

Bladder cancer - presentation? Ix? Mx?

A

Most common = transitional cell carcinoma (urothelial)

Presentation:

  • Painless visible haematuria (or asymptomatic non-visible haematuria)
  • Irrigative LUTS (urgency, suprapubic pain)
  • Recurrent UTIs
  • Pain, weight loss, lymphoedema

Ix:

  • Initial:
    • Urine dip (blood, leucocytes)
    • MC&S (use MSU - RBCs & WBCs, no bacterial growth)
    • Bloods - FBC
  • Flexible cystoscopy (lower urinary tract) + CT-urogram (upper urinary track if visible haematuria –> if non-visible low-risk use US)
  • Dx & staging = Transurethral Bladder Tumour Resection (TURBT) - resects full tumour + histology
    • Intravesical therapy:
      • Bacillus Calmette-Guerin (BCG) instilled into bladder –> reduces superficial bladder cancer recurrence (causes immune response to remaining tumour cells, same substance as in BCG vaccine)
      • Mitomycin - cytotoxic chemo agent

Mx: 2wk wait urology

  • Muscle invasive = cystectomy (young people) or radiotherapy/chemotherapy (older)
  • Superficial = surveillance cystoscopies, intravesical chemo
  • Mets = systemic therapy
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8
Q

AD Polycystic Kidney Disease (ADPKD)

Presentation? Associations? Screening?

A

ADPKD - Most freq genetic cause of renal failure in adults (abn chr 16)
* Cysts in kidneys and other organs (liver/pancreas/spleen)
* Associations - hepatic cysts, berry aneurysms (risk of ICH), mitral valve prolapse
* PC: haematuria (cyst rupture), flank pain (growing cyst), HTN (cysts prod renin), FHx - ICH
* Imaging including family screening - renal USS
* Tx: supportive

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9
Q

Testicular torsion - presentation? Tx?

A

Presentation: sudden-onset pain, high fixed position, absent cremasteric reflex

Tx: bilateral orchidopexy (both sides as increased risk of torsion in the other side)

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10
Q

What is paraphimosis? Causes? Pathophysiology? Mx?

A

Paraphimosis def: unable to pull back the foreskin

Causes: tight foreskin (phimosis), a complication of urinary catheter (always remember to replace foreskin after withdrawing for catheter insertion)

Pathophysiology: constrictive effect of foreskin –> oedema of distal penis –> ischaemia/necrosis (if severe)

Mx: UROLOGICAL EMERGENCY - must be reduced ASAP

  • Reduce with - Lubricating jelly OR dextrose-soaked gauze
  • If difficult - needle used to make small holes in penis –> drainage of oedema
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11
Q

Prostate cancer - Ix? Mx?

A

Ix:

  • PR exam, PSA
  • FBC, U&E, LFTs
  • Transrectal ultrasound (TRUS)-guided needle biopsy
    • Gleason score = PC grading
    • TNM staging
  • Multiparametric MRI

Mx: surgery/radiotherapy

  • Radial prostatectomy ± LN dissection
  • External beam radiotherapy/brachytherapy
  • Androgen-deprivation therapy (ADT)
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12
Q

Urinary incontinence - types & Tx?

A

Stress incontinence (leak on laugh/cough):

  • Pelvic muscle exercises
  • Pseudoephedrine (2nd - Duloxetine)
  • Retropubic suspension/colposuspension

Urge incontinence (preceded by the urge to pass urine):

  • Bladder retraining
  • Anticholinergic e.g. Oxybutynin (not if >80yrs), Tolterodine

Overactive bladder syndrome (urge but not incontinence - increased freq + nocturia): same as urge incontinence

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13
Q

Glomerular disease - nephrotic vs nephritic syndrome

A

Nephritic syndromes - blood/protein loss

Post-streptococcal glomerulonephritis
*** 2wks after streptococcal tonsilitis **(GAS)/skin infection
* Presentation: oedema, HTN, macroscopic haematuria, proteinuria
* Ix: low C3 lvls, high ASOT
* Mx: BP control

IgA nephropathy (Berger’s disease)
* PC: 24-48hrs after URTI/GI infection -> visible haematuria + flank pain

Granulomatosis with polyangitis (Wegener’s granulomatosis)
* Systemic vasculitis of small/medium vessels
* Triad: upper & lower resp involvement + glomerulonephritis +/ cutaneous/ocular/MSK/PNS

Eosinophilic granulomatosis with polyangitis (Churg-Strauss syndrome)
* Vasculitis + Asthma + Eosinophilia +/- GI/cardiac involvement
* Ix: p-ANCA (perinuclear anti-neutrophil cytoplasmic Abs)

Alport’s syndrome - X-linked hereditary (type IV collagen, mainly affects boys)
* Glomerulonephritis (intermittent visible haematuria in infancy) + SN hearing loss +/- eye abn

Anti-glomerular basement membrane ab disease (Goodpasture’s disease)
* Triad: glomerulonephritis, pul haemorrhage, anti-GDM ab formation

Nephrotic syndrome - urinary protein loss >3.5g/day, low albumin, oedema

Minimal change disease (most common nephrotic in kids)
* SBAs: swollen eyes/testes, 3+ protein on urine dip
* Features: proteinuria, oedema (periorbital/scrotal), low albumin (<30), high lipids, thrombophilia
* Ix: renal biopsy - electron microscopy = fusion of epithelial podocytes “minimal change as such minimal change in pathology”
* Mx: CS (pred)

Focal segmental glomerulosclerosis (most common nephrotic in adults)
* Caused by podocyte injury in glomeruli
* Can be primary (idiopathic) or secondary to HIV/obesity/meds

Membranous nephropathy (common nephrotic in adults)
* Mx: low-risk - conservative, high-risk - CS + cytotoxic/cyclosporin

Diabetic nephropathy - often aSx - foamy urine

AL amyloidosis - extracellular deposition of insoluble abn proteins (commonly AA), kidneys most commonly affected
* PC: very variable - WL, fatigue, oedema (resistant to diuretics)
* Ix: congo red staining + polarised light -> green fluorescence
* Mx: chemo/stem cell reconstitution

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14
Q

Hallmark feature of genitourinary TB?

A

Sterile pyuria

Normally presents as repeated UTIs resistant to typical abx

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15
Q

UTI Dx & management
Pyelonephritis Mx

A

If female + uncomplicated <65yrs/uncatheterised -> urine dip:
* +ve nitrites/leuk + RBC -> UTI likely
* +ve leuk, -ve nitrites -> UTI possible
* If all -ve UTI unlikely

If male do not use urine dip to dx (if not catheterised/>65yrs/indwelling catheter) and don’t start abx until urine culture confirms Dx

Mx: nitrofurantoin 3d (if eGFR ≥45, C/I: G6PD def/acute porphyria), 2nd - trimethoprim 3d (eGFR 15-30 use half dose after 3 days, <15 - use half dose)
* 7d tx in men, use nitro if pregnant (except at term)

Pyelonephritis (E. coli/Kleb) Mx: Cefalexin 7-10d

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16
Q

Renal artery stenosis overview

A

RAS - narrowing of renal artery lumen (sign if ≥50% reduction) due to atherosclerosis/fibromuscular dysplasia -> ↓ renal blood flow -> ↓ renal function -> ischaemic nephropathy & HTN (high renin/ANG-II)
* PC: asymptomatic - uncontrollable HTN, worsening eGFR (esp after starting ACEi), recurrent flash pul oedema
* Ix: Dx via imaging
* Mx: HTN-meds, aspirin + statins +/- angioplasty & stenting ONLY if HTN despite aggressive meds/rapidly declining eGFR/recurrent flash pul oedema

17
Q

Fanconi syndrome summary

A

Fanconi syndrome - inh/acquired disturbance of renal tubular transport -> aminoaciduria, glycosuria, phosphaturia, renal tubular acidosiis T2 (proximal)
* PC: polyuria, polydipsia, bouts of dehydration +/- fever, bone deformities (Ricket’s in kids, ostemalacia in adults)
* Mx: replacing lost substances + TX cause