30 types of urine system disease kidney urine bladder prostrate most important disease treatment investigation finding differential diagnosis contraindication ICO management OPD prescription

Reading File
Finding Sources
Finding Sources
Finding Sources
The library confirms excellent nephrology and urology sources. Drawing on the confirmed textbooks (Brenner & Rector's The Kidney, Comprehensive Clinical Nephrology 7e, Campbell-Walsh Urology, Goldman-Cecil Medicine, Harrison's, NKF Primer, Robbins Pathology), here is the comprehensive reference:

30 Urinary System Diseases — Clinical Reference

KIDNEY DISEASES


1. ACUTE KIDNEY INJURY (AKI)

Definition: Sudden decline in renal function (↑Creatinine ≥0.3 mg/dL in 48h or ↑50% in 7 days, or UO <0.5 mL/kg/hr for 6h).
Classification: Pre-renal | Intrinsic (ATN, GN, AIN) | Post-renal
Investigations:
  • Serum Cr, BUN, eGFR, electrolytes, ABG
  • Urine: dipstick, microscopy (muddy brown casts = ATN), Na, FENa, osmolality
  • Renal USS (obstruction, size)
  • FENa: <1% = pre-renal; >2% = intrinsic ATN
Key Findings:
  • Oliguria/anuria, oedema, hypertension
  • Hyperkalaemia, metabolic acidosis, hyperphosphataemia
  • BUN:Cr ratio >20:1 → pre-renal
Differential Diagnosis: CKD, pre-renal azotaemia, obstructive uropathy, HRS
Treatment/Management:
  • Remove precipitant; IV fluids (pre-renal)
  • Loop diuretics (volume overload)
  • Treat hyperkalaemia (calcium gluconate, insulin+dextrose, salbutamol, kayexalate)
  • Dialysis (AEIOU criteria: Acidosis, Electrolytes, Intoxication, Overload, Uraemia)
  • Avoid nephrotoxins (NSAIDs, aminoglycosides, contrast)
OPD Prescription:
  • Furosemide 40 mg BD PO (if fluid overloaded)
  • Sodium bicarbonate 500 mg TDS (acidosis)
  • Monitor U&E twice weekly
Contraindications: ACEi/ARBs in bilateral RAS; NSAIDs; IV contrast without hydration

2. CHRONIC KIDNEY DISEASE (CKD)

Definition: GFR <60 mL/min/1.73m² or kidney damage markers for >3 months.
Stages: G1 (≥90) → G5 (<15) | Albuminuria: A1-A3
Investigations:
  • eGFR (CKD-EPI), urine ACR, 24-hr urine protein
  • Renal USS: small, echogenic kidneys
  • Renal biopsy (if unclear aetiology)
  • FBC (normocytic anaemia), PTH, phosphate, Ca, Vit D, bicarbonate
Key Findings:
  • Uraemic symptoms: fatigue, nausea, pruritus, uraemic frost
  • Anaemia, renal osteodystrophy, CKD-mineral bone disease
  • Hypertension, fluid retention
Differential: Diabetic nephropathy, HTN nephrosclerosis, renovascular disease, ADPKD
Treatment:
  • BP control: ACEi/ARB (target <130/80)
  • SGLT2 inhibitors (dapagliflozin — CKD G3-G4 with proteinuria)
  • Anaemia: EPO + IV iron (target Hb 10-12 g/dL)
  • Phosphate binders (sevelamer), Vit D analogue (alfacalcidol)
  • Low-protein diet (0.6-0.8 g/kg/day)
  • Dialysis/transplant at G5
OPD Prescription:
  • Ramipril 5 mg OD (or losartan 50 mg OD)
  • Dapagliflozin 10 mg OD
  • Ferrous sulphate 200 mg TDS
  • Calcium carbonate 500 mg with meals (phosphate binder)
  • Alfacalcidol 0.25 mcg OD
Contraindications: Metformin if eGFR <30; NSAIDs; high-K+ diet with ACEi

3. NEPHROTIC SYNDROME

Definition: Proteinuria >3.5 g/day + hypoalbuminaemia + oedema + hyperlipidaemia.
Causes: MCD (children), FSGS, MN, diabetic nephropathy, amyloidosis, lupus
Investigations:
  • 24-hr urine protein or spot urine PCR >300 mg/mmol
  • Serum albumin <25 g/L
  • Fasting lipids (hypercholesterolaemia), LFT
  • Complement (C3/C4 low in SLE, MPGN)
  • Renal biopsy (essential in adults)
  • ANA, anti-dsDNA, SPEP, hepatitis B/C, HIV
Key Findings:
  • Pitting oedema (periorbital initially in children)
  • Frothy urine, lipiduria (Maltese cross on polarised)
  • Oval fat bodies on urinary microscopy
Differential: Cirrhosis, CCF, protein-losing enteropathy, nephritic syndrome
Treatment:
  • MCD: Prednisolone 1 mg/kg/day → taper over 3-6 months
  • FSGS: Prednisolone; cyclosporine if resistant
  • MN: KDIGO Ponticelli protocol (steroids + chlorambucil alternating)
  • Diuretics (furosemide + spironolactone for oedema)
  • ACEi/ARB (reduce proteinuria)
  • Statins (dyslipidaemia), anticoagulation (high DVT risk, especially MN)
OPD Prescription:
  • Prednisolone 60 mg OD (MCD — 4-6 weeks then taper)
  • Furosemide 40 mg OD
  • Spironolactone 25 mg OD
  • Atorvastatin 20 mg nocte
  • Ramipril 5 mg OD
Contraindications: Live vaccines during immunosuppression; NSAIDs (worsen oedema, AKI risk)

4. NEPHRITIC SYNDROME

Definition: Haematuria (RBC casts), proteinuria <3.5 g/day, hypertension, oliguria, oedema.
Causes: Post-streptococcal GN, IgA nephropathy, lupus nephritis, ANCA vasculitis, anti-GBM disease
Investigations:
  • Urinalysis: dysmorphic RBCs, RBC casts
  • ASO titre, anti-DNase B (post-strep)
  • ANA, anti-dsDNA, ANCA (PR3/MPO), anti-GBM
  • C3/C4 (low in SLE, post-strep, MPGN)
  • Renal biopsy (definitive)
Key Findings:
  • "Cola/tea-coloured" urine, hypertension, oliguria
  • Light microscopy: hypercellular glomeruli (post-strep); crescents (RPGN)
  • IF: "lumpy bumpy" granular (post-strep); linear (Goodpasture)
Differential: Nephrotic syndrome, haemorrhagic cystitis, IgA nephropathy, thin basement membrane disease
Treatment:
  • PSGN: supportive (salt/fluid restriction, antihypertensives, penicillin for active strep)
  • RPGN (crescentic GN): IV methylprednisolone + cyclophosphamide; plasma exchange (anti-GBM, ANCA)
  • Lupus nephritis: MMF or cyclophosphamide + steroids
  • IgA nephropathy: ACEi/ARB, fish oil, steroids if proteinuria >1 g/day
OPD Prescription:
  • Amlodipine 5 mg OD (BP control)
  • Ramipril 5 mg OD (proteinuria)
  • Prednisolone 1 mg/kg/day (when indicated)
Contraindications: Cyclophosphamide in pregnancy; live vaccines

5. IgA NEPHROPATHY (Berger's Disease)

Key Features: Most common primary GN worldwide; episodic gross haematuria with URTI (synpharyngitic haematuria).
Investigations: Renal biopsy — mesangial IgA deposits on IF; raised serum IgA (50%)
Differential: Post-strep GN (delayed haematuria), thin BM disease, Alport syndrome, HSP
Treatment: ACEi/ARB (proteinuria <1 g/day); steroids + fish oil (proteinuria 1-3 g); SGLT2i; Sparsentan (novel DUAL Ang/ET receptor antagonist, FDA 2023)

6. LUPUS NEPHRITIS

Classes (ISN/RPS): I–VI (Class III/IV most severe — proliferative)
Investigations: ANA, anti-dsDNA, anti-Sm, C3/C4 low, renal biopsy, urine PCR
Treatment:
  • Induction: MMF 3 g/day + prednisolone OR IV cyclophosphamide (NIH protocol)
  • Maintenance: MMF 2 g/day + low-dose steroid
  • Hydroxychloroquine (all patients — renoprotective)
  • Belimumab (adjunctive in active disease)

7. DIABETIC NEPHROPATHY

Stages: Microalbuminuria (ACR 3-30 mg/mmol) → Macroalbuminuria → Declining GFR
Investigations: Annual urine ACR, eGFR, HbA1c, fundoscopy (retinopathy co-exists)
Pathology: Kimmelstiel-Wilson nodules (nodular glomerulosclerosis), GBM thickening
Treatment: Tight glycaemic control (HbA1c <53 mmol/mol); ACEi/ARB; SGLT2i (empagliflozin, dapagliflozin); Finerenone (novel MRA — reduces CKD progression in DM)
Contraindications: SGLT2i if eGFR <20; Metformin if eGFR <30

8. HYPERTENSIVE NEPHROSCLEROSIS

Features: Long-standing HTN → afferent arteriolar thickening → nephron loss; mild proteinuria, slowly declining eGFR
Investigations: Renal USS (mildly small, echogenic), bland urinalysis, normal C3/C4
Treatment: BP target <130/80; ACEi/ARB first-line; low-salt diet

9. POLYCYSTIC KIDNEY DISEASE (ADPKD)

Gene: PKD1 (85%, chr 16), PKD2 (15%, chr 4)
Features: Bilateral multiple renal cysts, HTN, haematuria, abdominal mass, flank pain, recurrent UTI, renal calculi
Extra-renal: Hepatic cysts, intracranial berry aneurysms, mitral valve prolapse
Investigations: USS (>2 cysts per kidney in <30 yrs, >4 cysts per kidney in >60 yrs); MRI; genetic testing (PKD1/2)
Differential: Simple renal cysts, tuberous sclerosis, von Hippel-Lindau
Treatment: Tolvaptan (V2 receptor antagonist — slows cyst growth; licensed if rapidly progressive, Toronto class 1C-E); ACEi/ARB; analgesics; treat complications; dialysis/transplant
Contraindications: Tolvaptan — hepatotoxicity risk (monitor LFTs monthly for 18 months); avoid nephrotoxins

10. RENAL TUBULAR ACIDOSIS (RTA)

Types:
TypeDefectUrine pHSerum K+
1 (Distal)H+ secretion failure>5.5Low
2 (Proximal)HCO3 reabsorption failure<5.5Low
4Aldosterone deficiency/resistance<5.5High
Causes: Sjogren's, SLE, medullary sponge kidney (Type 1); Wilson's, Fanconi (Type 2); DM, CAH (Type 4)
Investigations: ABG (NAGMA), urine pH, serum electrolytes, urine anion gap (positive = distal RTA)
Treatment: Sodium bicarbonate (Type 1 & 2); fludrocortisone (Type 4); potassium citrate (nephrolithiasis)

11. ACUTE TUBULAR NECROSIS (ATN)

Causes: Ischaemia (post-shock, sepsis), nephrotoxins (aminoglycosides, cisplatin, contrast, myoglobin)
Investigations: Muddy brown granular casts, FENa >2%, renal USS (normal size)
Phases: Initiation → Oliguric (1-3 wks) → Polyuric (diuresis phase) → Recovery
Treatment: Supportive — fluid management, avoid nephrotoxins, dialysis if needed; N-acetylcysteine (prevention of contrast nephropathy)

12. INTERSTITIAL NEPHRITIS (AIN)

Causes: Drug-induced (NSAIDs, PPIs, penicillins, sulfonamides), infections, autoimmune (Sarcoid, SLE, Sjogren's)
Investigations: Urine eosinophils (unreliable); eosinophilia; raised Cr; renal biopsy (interstitial inflammation + eosinophils)
Treatment: Stop offending drug; prednisolone 1 mg/kg/day if severe or no improvement at 2 weeks

13. RENOVASCULAR DISEASE / RENAL ARTERY STENOSIS

Causes: Atherosclerosis (elderly), fibromuscular dysplasia (young women)
Features: Resistant hypertension, flash pulmonary oedema, deterioration with ACEi/ARB
Investigations: Duplex USS (screening); CT angiography or MR angiography (gold standard); captopril renogram
Treatment: Medical (ACEi/ARB — caution bilateral); percutaneous transluminal angioplasty ± stenting (FMD); revascularisation (atherosclerotic — limited evidence)
Contraindications: ACEi/ARB absolutely contraindicated in bilateral RAS (causes AKI)

14. RENAL CALCULI (Nephrolithiasis)

Types: Calcium oxalate (70%), Struvite/triple phosphate (infection), Uric acid, Cystine
Features: Loin-to-groin colicky pain, haematuria, N&V, dysuria
Investigations:
  • NCCT KUB (gold standard — detects all stones)
  • USS + KUB X-ray (initial)
  • Urine dipstick (blood), MSU, serum Ca, urate, oxalate
  • 24-hr urine (Ca, oxalate, uric acid, citrate, volume)
Stone characteristics on X-ray:
  • Radiopaque: calcium oxalate, calcium phosphate
  • Radiolucent: uric acid, cystine (semi-opaque)
  • Staghorn calculus: struvite
Differential: Ureteric colic, appendicitis, ovarian cyst, pyelonephritis, AAA
Treatment:
  • <5 mm: conservative (fluids, analgesia — diclofenac 75 mg IM/PR, tamsulosin 0.4 mg OD — alpha-blocker MET)
  • 5-10 mm: tamsulosin ± ESWL
  • 10 mm / complex: ESWL, ureteroscopy, PCNL (>2 cm)
  • Struvite: treat infection + stone removal
  • Uric acid: urine alkalinisation (potassium citrate), allopurinol
  • Prevention: high fluid intake >2.5 L/day, low salt, low oxalate diet, thiazide (Ca stones), allopurinol (uric acid)
OPD Prescription:
  • Diclofenac 50 mg TDS PRN + PPI cover
  • Tamsulosin 0.4 mg OD (MET)
  • K-citrate 15 mEq BD (uric acid/cystine stones)
Contraindications: NSAIDs in renal impairment; ESWL in pregnancy, bleeding disorders, distal obstruction, abdominal aortic aneurysm

15. PYELONEPHRITIS

Features: Fever, rigors, loin pain, CVA tenderness, dysuria, frequency
Investigations:
  • Urinalysis (leucocytes, nitrites, blood)
  • MSU M&C&S (most important)
  • Blood cultures (if systemically unwell)
  • USS/CT (complicated: obstruction, abscess, emphysematous pyelonephritis)
  • WBC, CRP, procalcitonin
Common Organism: E. coli (80%), Klebsiella, Proteus, Enterococcus
Differential: Appendicitis, cholecystitis, ovarian pathology, diverticulitis, renal colic, perinephric abscess
Treatment:
  • Uncomplicated (outpatient): Trimethoprim 200 mg BD × 14 days OR ciprofloxacin 500 mg BD × 7 days
  • Complicated/Inpatient: IV ceftriaxone 1-2 g OD or IV gentamicin (dose-adjust for renal function)
  • Duration: 7-14 days; 14 days for complicated
OPD Prescription:
  • Ciprofloxacin 500 mg BD × 7 days (after MSU)
  • Paracetamol 1 g QDS PRN
  • Increase oral fluid intake >2 L/day
Contraindications: Fluoroquinolones in children, pregnancy (use cephalosporins); trimethoprim in 1st trimester (folate antagonist)

16. RENAL CELL CARCINOMA (RCC)

Classic Triad: Haematuria + loin pain + flank mass (only 10% — late presentation)
Subtypes: Clear cell (70%), papillary (15%), chromophobe (5%)
Investigations:
  • CT chest/abdomen/pelvis with contrast (staging + surgical planning)
  • MRI (IVC involvement)
  • Renal biopsy (if metastatic — confirm histology before systemic therapy)
  • Urine cytology (negative — not useful)
  • Paraneoplastic: polycythaemia, hypercalcaemia, HTN, Stauffer syndrome (liver dysfunction)
Differential: TCC of renal pelvis, oncocytoma, angiomyolipoma, Wilms (children)
Treatment:
  • Localised: Radical or partial nephrectomy (laparoscopic preferred)
  • Metastatic: Sunitinib/pazopanib (TKI, 1st line), ipilimumab + nivolumab (IO combination), everolimus (2nd line)
  • Adjuvant: pembrolizumab post-nephrectomy (high risk)
Contraindications: TKIs — hepatotoxicity; bevacizumab — uncontrolled HTN, bleeding, fistula

17. GLOMERULOSCLEROSIS (FSGS)

Features: Nephrotic syndrome, resistant to steroids in adults; HIV-associated FSGS (collapsing variant)
Biopsy: Focal (some glomeruli) + segmental (part of glomerulus) sclerosis on LM; effacement of foot processes on EM
Treatment: Prednisolone 1 mg/kg/day × 4-6 months; cyclosporine/tacrolimus (steroid-resistant); ACEi/ARB; sparsentan (FDA 2023)

18. MINIMAL CHANGE DISEASE (MCD)

Features: Commonest cause of nephrotic syndrome in children; sudden onset heavy proteinuria; responds to steroids
Biopsy: Normal LM; podocyte foot process effacement on EM; no IF deposits
Treatment: Prednisolone 60 mg/m² OD × 4-6 weeks → taper; levamisole (maintenance, steroid-sparing in children); cyclophosphamide (frequent relapser)

19. MEMBRANOUS NEPHROPATHY (MN)

Features: Commonest cause of nephrotic syndrome in white adults; associated with anti-PLA2R antibody (70%); secondary causes: HBV, malignancy, SLE, drugs (gold, penicillamine)
Biopsy: "Spike and dome" appearance on silver stain; IgG + C3 granular deposits on IF; subepithelial deposits on EM
Treatment: ACEi/ARB + supportive (spontaneous remission 30%); KDIGO modified Ponticelli (steroids + chlorambucil, 6 months) for severe disease; Rituximab (anti-CD20 — increasingly used, non-inferior to Ponticelli)

20. ALPORT SYNDROME

Genetics: X-linked (80%) — COL4A5 mutation; AR — COL4A3/4 mutation
Features: Haematuria (persistent) + SNHL + ocular abnormalities (anterior lenticonus); family history of renal failure
Biopsy: Irregular thinning + thickening of GBM with splitting (basket-weave) on EM; absent type IV collagen on IF
Treatment: ACEi/ARB (delays progression); dialysis/transplant; genetic counselling

BLADDER DISEASES


21. URINARY TRACT INFECTION (LOWER UTI / CYSTITIS)

Features: Dysuria, frequency, urgency, suprapubic pain, cloudy/smelly urine; NO systemic features
Organisms: E. coli (80%), Staphylococcus saprophyticus (young women), Klebsiella
Investigations:
  • Urine dipstick (nitrites + leucocytes — 85% sensitive)
  • MSU M&C&S (gold standard; indicated in complicated UTI, pregnancy, recurrent, men, children)
Differential: Urethritis (STI — Chlamydia, Gonorrhoea), interstitial cystitis, overactive bladder, vaginitis, bladder cancer (painless haematuria)
Treatment:
  • Uncomplicated women: Trimethoprim 200 mg BD × 3 days OR nitrofurantoin 100 mg MR BD × 3 days
  • Recurrent UTI: Post-coital prophylaxis (nitrofurantoin 50 mg), long-term low-dose prophylaxis, D-mannose
  • Pregnant: Nitrofurantoin × 7 days (avoid near term); cephalexin 500 mg QDS × 7 days
  • Men: Ciprofloxacin 500 mg BD × 7 days (exclude prostatitis)
OPD Prescription:
  • Nitrofurantoin 100 mg MR BD × 3 days (uncomplicated female)
  • Trimethoprim 200 mg BD × 3 days (alternative)
  • Paracetamol 1 g QDS + increase fluid intake
Contraindications: Nitrofurantoin — eGFR <30 (ineffective + risk of neuropathy); avoid in late pregnancy (neonatal haemolysis); trimethoprim — 1st trimester, hyperkalaemia risk with ACEi

22. INTERSTITIAL CYSTITIS / BLADDER PAIN SYNDROME

Features: Chronic bladder pain (>6 months), urinary urgency/frequency, sterile urine; predominantly women
Investigations: Cystoscopy + hydrodistension (Hunner lesions), urine cytology (exclude TCC), MSU (exclude infection), urodynamics
Differential: UTI, overactive bladder, bladder cancer, endometriosis, pelvic floor dysfunction
Treatment: Bladder retraining; intravesical instillations (DMSO, hyaluronic acid); pentosan polysulphate sodium (Elmiron) PO; amitriptyline 25-75 mg nocte; cyclosporine A; neuromodulation; cystectomy (last resort)

23. BLADDER CANCER

Risk Factors: Smoking (#1), aniline dyes (occupational), schistosomiasis (SCC), cyclophosphamide, phenacetin
Features: Painless haematuria (frank or microscopic) — "must rule out cancer"
Types: TCC/Urothelial (90%), SCC (Schistosoma), Adenocarcinoma
Staging:
  • Non-muscle invasive (NMIBC): Ta, T1, CIS
  • Muscle-invasive (MIBC): T2-T4
Investigations:
  • Flexible cystoscopy (gold standard)
  • CT urogram (upper tract assessment)
  • Urine cytology (high-grade/CIS)
  • TURBT (transurethral resection — diagnosis + staging)
Differential: UTI, renal calculi, RCC, prostatitis, BPH, ureteric TCC, endometriosis
Treatment:
  • NMIBC Ta low grade: TURBT ± intravesical mitomycin C (single dose)
  • NMIBC high grade/CIS/T1: TURBT + BCG immunotherapy × 6 weeks induction + maintenance × 3 years
  • MIBC T2-T4: Radical cystectomy (neoadjuvant cisplatin-based chemo → gemcitabine + cisplatin)
  • Metastatic: Cisplatin + gemcitabine; pembrolizumab (2nd line or cisplatin-ineligible); enfortumab vedotin + pembrolizumab (1st line, FDA 2023)
Contraindications: BCG — immunocompromised, active UTI, traumatic catheterisation, TB history; Cisplatin — eGFR <50

24. OVERACTIVE BLADDER (OAB)

Features: Urgency ± urge incontinence + frequency + nocturia; no infection
Investigations: Urine dipstick + MSU (exclude UTI); bladder diary; urodynamics (detrusor overactivity)
Treatment:
  • Conservative: Bladder retraining, pelvic floor exercises, fluid/caffeine restriction
  • Pharmacological: Solifenacin 5 mg OD (M3 antagonist) OR mirabegron 50 mg OD (β3-agonist) — preferred if dry mouth/cognition concerns
  • Intravesical Botox (onabotulinumtoxin A 100 units) — refractory
  • PTNS (percutaneous tibial nerve stimulation); sacral neuromodulation
Contraindications: Antimuscarinics — narrow-angle glaucoma, urinary retention, GI obstruction, cognitive impairment (elderly); avoid oxybutynin in elderly (anticholinergic burden)

25. NEUROGENIC BLADDER

Causes: Spinal cord injury, MS, Parkinson's, DM autonomic neuropathy, spina bifida
Types: Spastic (upper motor neuron — urgency, small capacity) vs Flaccid (LMN — retention, overflow)
Investigations: Urodynamics (gold standard); USS post-void residual (PVR); MRI spine
Treatment: Clean intermittent catheterisation (CIC — gold standard); antimuscarinics (spasticity); alpha-blockers (outflow); intravesical Botox; sphincterotomy; suprapubic catheter

PROSTATE DISEASES


26. BENIGN PROSTATIC HYPERPLASIA (BPH)

Features: Obstructive: hesitancy, weak stream, terminal dribbling, incomplete emptying; Irritative: frequency, urgency, nocturia; Middle-age+ men
Investigations:
  • DRE (enlarged, smooth, non-tender — "rubbery")
  • PSA (to exclude PCa — if PSA raised, consider biopsy)
  • USS abdomen + post-void residual
  • IPSS (International Prostate Symptom Score)
  • Flow rate (urodynamics if uncertain)
  • Urine dipstick + MSU
Differential: Prostate cancer, prostatitis, urethral stricture, neurogenic bladder, bladder cancer, bladder neck obstruction
Treatment:
  • Mild (IPSS <8): Watchful waiting + lifestyle (fluid restriction, double voiding)
  • Alpha-blockers: Tamsulosin 0.4 mg OD (rapid onset, relax smooth muscle) — first-line
  • 5-alpha reductase inhibitors: Finasteride 5 mg OD or dutasteride 0.5 mg OD (shrink gland; for large prostate >40 mL; 6+ month onset)
  • Combination: Tamsulosin + finasteride (large gland, high PSA, prevention of AUR)
  • Tadalafil 5 mg OD (if concurrent erectile dysfunction)
  • Surgery: TURP (gold standard surgical Rx), HoLEP, UroLift, Rezum (steam injection)
  • Acute urinary retention: Urethral catheter (if fails → suprapubic) → trial without catheter (TWOC) after alpha-blocker
OPD Prescription:
  • Tamsulosin 0.4 mg OD (MR)
  • Finasteride 5 mg OD (if prostate >40 mL)
  • Mirabegron 50 mg OD (if persistent irritative symptoms)
Contraindications: Alpha-blockers — postural hypotension, caution with antihypertensives and PDE5i; 5-ARIs — not in pregnancy (teratogenic — use gloves); PSA halved by 5-ARIs (adjust accordingly)

27. PROSTATE CANCER (PCa)

Features: Often asymptomatic early; LUTS (obstruction), bone pain (metastases — lumbar spine, pelvis), haematuria, haematospermia, erectile dysfunction
Investigations:
  • PSA (age-adjusted; PSA density, PSA velocity, free:total PSA ratio)
  • DRE (irregular, hard, asymmetric — "craggy" nodule)
  • MRI prostate (multi-parametric MRI — PI-RADS score; pre-biopsy staging)
  • TRUS-guided or MRI-fusion targeted biopsy (diagnosis + Gleason grading)
  • Bone scan + CT (if PSA >10, Gleason >7, or N/M staging)
  • Gleason score (2-10) → Grade groups 1-5
Staging: T1-T4 | N0-N1 | M0-M1
Differential: BPH, prostatitis, UTI, bladder cancer, seminal vesicle pathology
Treatment:
  • Low risk (Gleason 6, PSA <10): Active surveillance (PSA every 6 months, repeat MRI/biopsy)
  • Intermediate/High risk localised: Radical prostatectomy (RP) OR external beam radiotherapy (EBRT) + ADT × 6-18 months
  • Locally advanced: EBRT + long-term ADT (2-3 years)
  • Metastatic hormone-sensitive (mHSPC): ADT (LHRH agonist — leuprorelin/goserelin OR bilateral orchidectomy) + docetaxel OR abiraterone OR darolutamide
  • Castration-resistant (mCRPC): Abiraterone + prednisolone; enzalutamide; docetaxel; radium-223 (bone mets); PARP inhibitors (olaparib — BRCA mutation)
OPD Prescription (ADT + AR pathway):
  • Leuprorelin 3.75 mg SC monthly (LHRH agonist) + bicalutamide 50 mg OD (flare cover × 4 wks)
  • Abiraterone 1000 mg OD + prednisolone 5 mg BD (mCRPC/mHSPC)
  • Zoledronic acid 4 mg IV 4-weekly (bone protection)
  • Calcium + Vit D (bone health on ADT)
Contraindications: LHRH agonists — testosterone flare (cover with anti-androgen 1st week); enzalutamide — severe hepatic impairment, seizures; olaparib — concurrent CYP3A4 inhibitors without dose adjustment

28. PROSTATITIS

Types:
TypeFeatures
I — Acute bacterialFever, chills, perineal pain, dysuria, acute ill, DRE tender (do NOT massage!)
II — Chronic bacterialRecurrent UTI, pelvic/perineal pain, raised PSA
III — Chronic pelvic pain syndrome (CPPS)Pain >3 months, sterile cultures — most common (95%)
IV — Asymptomatic inflammatoryIncidental finding on biopsy
Investigations:
  • MSU, blood cultures (Type I)
  • Meares-Stamey 4-glass test or 2-glass pre/post-prostate massage test (Type II/III)
  • USS (exclude abscess), PSA (raised acutely)
Differential: BPH, PCa, seminal vesicle cyst, pudendal neuralgia, bladder cancer, STI
Treatment:
  • Acute bacterial: IV ceftriaxone → ciprofloxacin 500 mg BD × 4-6 weeks
  • Chronic bacterial: Ciprofloxacin 500 mg BD × 4-6 weeks OR trimethoprim × 12 weeks
  • CPPS: Alpha-blockers (tamsulosin) + anti-inflammatories + pelvic floor physio + amitriptyline/gabapentin (neuropathic component); 5-ARIs; CBT
  • Prostatic abscess: TRUS-guided drainage
Contraindications: Prostatic massage in Type I (risk of septicaemia); fluoroquinolones — prolonged QT

29. ERECTILE DYSFUNCTION / PROSTATE-RELATED SEXUAL DYSFUNCTION

Features: Post-RP incontinence + ED; ED in chronic prostatitis; hormonal (post-ADT)
Treatment:
  • PDE5 inhibitors: Sildenafil 50 mg PRN, tadalafil 5 mg OD (concurrent BPH)
  • Vacuum erection devices; intracavernosal alprostadil; penile implant
  • Post-RP: early penile rehabilitation
Contraindications: PDE5i — absolute CI with nitrates (hypotension risk); caution with alpha-blockers

URETERS & COLLECTING SYSTEM


30. VESICOURETERAL REFLUX (VUR)

Definition: Retrograde flow of urine from bladder to ureter/kidney
Grades: I (ureter only) → V (severe — dilated, tortuous ureter + intrarenal reflux)
Features: Recurrent febrile UTI in children; renal scarring → reflux nephropathy → HTN, proteinuria, CKD
Investigations:
  • Micturating cystourethrogram (MCUG) — gold standard diagnosis
  • DMSA isotope scan (renal scarring — most sensitive)
  • USS (dilatation — poor sensitivity for VUR)
  • MAG3 renogram (function + drainage)
Differential: Duplex collecting system, ureterocele, posterior urethral valves (boys), pelviureteric junction obstruction (PUJ)
Treatment:
  • Grade I-III: Antibiotic prophylaxis (trimethoprim 2 mg/kg nocte OR nitrofurantoin 1 mg/kg nocte) + surveillance; most resolve spontaneously
  • Grade IV-V / breakthrough infections / scarring: Endoscopic treatment (STING/HIT procedure — submucosal Deflux injection) OR ureteric reimplantation
Contraindications: Nitrofurantoin prophylaxis — eGFR <30 (ineffective); avoid in infants <3 months (haemolytic anaemia risk)

Quick Reference Summary Table

#DiseaseKey InvestigationFirst-Line Treatment
1AKIFENa, urine castsRemove cause; fluids; dialysis
2CKDeGFR, urine ACRACEi/ARB + SGLT2i
3Nephrotic SyndromeRenal biopsyPrednisolone (MCD)
4Nephritic SyndromeRenal biopsy, ANCA/ANASteroids ± cyclophosphamide
5IgA NephropathyBiopsy (mesangial IgA)ACEi/ARB; Sparsentan
6Lupus NephritisAnti-dsDNA, C3/C4, biopsyMMF + steroids
7Diabetic NephropathyUrine ACR, HbA1cACEi + SGLT2i + finerenone
8HTN NephrosclerosisUSS, bland urineBP control — ACEi/ARB
9ADPKDUSS / MRITolvaptan; ACEi
10RTAABG, urine pH, UAGNaHCO3 (Type 1/2); Fludrocortisone (Type 4)
11ATNFENa >2%, muddy castsSupportive; avoid nephrotoxins
12AINUrine eosinophils, biopsyStop drug; prednisolone
13Renal Artery StenosisCT/MR angiographyACEi (unilateral); angioplasty
14Renal CalculiNCCT KUBAnalgesia; MET (tamsulosin); ESWL/PCNL
15PyelonephritisMSU M&C&SCiprofloxacin/ceftriaxone
16RCCCT CAPNephrectomy; sunitinib/IO
17FSGSBiopsy (EM foot process effacement)Prednisolone; cyclosporine
18MCDBiopsy (normal LM, EM effacement)Prednisolone
19Membranous NephropathyAnti-PLA2R, biopsyRituximab/Ponticelli
20Alport SyndromeEM (basket-weave GBM)ACEi/ARB; transplant
21UTI/CystitisUrine dipstick + MSUNitrofurantoin/trimethoprim × 3 days
22Interstitial CystitisCystoscopy, Hunner lesionsAmitriptyline; intravesical DMSO
23Bladder CancerCystoscopy + TURBTTURBT ± BCG; radical cystectomy
24Overactive BladderUrodynamicsSolifenacin / mirabegron
25Neurogenic BladderUrodynamicsCIC; antimuscarinics
26BPHIPSS, PSA, USS PVRTamsulosin; finasteride; TURP
27Prostate CancerPSA, mpMRI, biopsyActive surveillance; RP/RT; ADT
28ProstatitisMSU, 4-glass testCiprofloxacin × 4-6 weeks
29ED (prostate-related)ClinicalPDE5i (sildenafil)
30Vesicoureteral RefluxMCUG, DMSA scanAntibiotic prophylaxis; STING/reimplant

Key Sources: Brenner & Rector's The Kidney (9780323532655) | Comprehensive Clinical Nephrology 7e (9780323825924) | Campbell-Walsh Urology (9780323546423) | Goldman-Cecil Medicine (9780323930345) | Harrison's IM 22e | Robbins Pathology | NKF Primer 8e (9780323791229)
This is a shared conversation. Sign in to Orris to start your own chat.