Urology Flashcards

1
Q

Causes of haematuria

A

Tumours - frank/microscopic, usually painless, carcinoma in situ of bladder usually causes micturition symptoms
Irritation from infection/stones - usually + dysuria
Prostatic enlargement - straining at micturition may dilate bladder neck veins
Trauma
Haemoglobinuria - red from Hb not blood, in young people excess exercise
Renal parenchymal inflammation
Micro-emboli in kidneys from AF, infective endocarditis§

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2
Q

What are the micturition symptoms?

A

Dysuria - pain/discomfort on micturition, often a/w difficulty voiding and burning/scalding pain. due to urethral irritation usually UTI, recent instrumentation or catheterisation
Frequency - frequently pass small volumes but normal overall daily volume. E.g. bladder irritation, incomplete emptying in BPH/MS, detrusor overactivity, fibrosed bladder e.g. schistosomiasis
Nocturia - HF, old age, drugs
Urgency - e.g. UTI, BPH
Hesitancy - BPH (not enough urine into proximal urethra to relax sphincter)
Poor stream - urethral compression or stricture
Post-micturition dribbling - weak bulbospongiosus, abnormal sphincter, pelvic floor weakness

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3
Q

Acute urinary retention?

A

Medical emergency: abrupt inability to PU over a period of hours. Usually painful

Causes:

  • infection/inflammatory: e.g. BPH (often acute on chronic picture), proctitis, vulvovaginitis, lichen planus, schistosomiasis, cystitis, primary HSVV, peri-urethral abscess
  • drug-related: anticholinergics, opioids, anaesthetic drugs, alpha agonists, BZDs, NSAIDs, detrusor relaxants, CCBs, antihistamines, alcohol
  • neurological (more often chronic tbh): autonomic/peripheral nerve (DM, GBS, pernicious anaemia, poliomyelitis), brain (CVD, MS, neoplasm, NPH, PD), SC (meningomyelocele, MS, SC haematoma, cauda equina)
  • post-op: common, due to pain, traumatic instrumentation, bladder overdistension, drugs
  • other: e..g penile #, postpartum complications, pelvic trauma

Ix: urinalysis, US bladder scan to see post-void residual volume, US KUB for hydronephrosis, CT AP to see bladder neck compression, cystoscopy

M: catheterise, treat cause, alpha blocker (Tamsulosin or alfuzosin), 5-alpha reductase inhibitors (finasteride), TWOC, if fails TURP

Comps: post-obstructive diuresis (causes electrolyte issues), post-retention haematuria, AKI, UTI

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4
Q

Chronic urinary retention?

A

Gradually develop inability to completely empty bladder causing residual volume >1L/distented bladder

Often painless. High pressure causes renal impairment. May get overflow voiding. If long term can get bladder diverticula-back pressure on kidneys-uraemia. At an point may get acute on chronic retention

Causes: structural/functional abnormalities of bladder muscle/sphincter, persistent urethral obstruction (e.g. BPH), lower spinal neuro problems

Management: intermittent catheter - then long term indwelling catheter, TURP if fit, drugs for BPH
*urethral catheterisation best, record residual volume, re-examine to ensure mass disappeared

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5
Q

Normal bladder capacity?

A

300-500ml

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6
Q

Micturition ?

A

Filling - detrusor muscle relaxes so pressure doesn’t rise until bladder near full
Detrusor contracts to void (both mediated by spinal reflex at S2-4)
Cortical conscious inhibitory control to delay voiding

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7
Q

What are the causes of urinary incontinence?

A
  1. Loss of cortical inhibitory control e.g. dementia, supra-sacral SC issue (e.g. MS, traumatic paraplegia)
  2. Abnormal sacral reflex: sacral neurogenic bladder (damaged reflex arc so large residual volume e.g. diabetic neuropathy, pelvic tumours, low trauma), overactive bladder (hypersensitive so get voiding reflex below capacity, urge incontinence, treat with antimuscarinics e.g. oxybutinin), infection, hypotonic bladder (from BPH persistent obstruction causing stretching)
  3. Detrusor/sphincter abnormalities: stress incontinence (weak sphincter pelvic floor damage), post-prostatectomy, tumour, urethral trauma, TB, radiotherapy, congenital e.g. epispadiasis
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8
Q

What may cause pneumaturia?

A

Fistulae - from diverticular disease, pericolic abscess in Crohns, colon/bladder cancer
– abnormal communication between bowel + UT

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9
Q

Renal trauma?

A

Minor trauma common to get microscopic haematuria
Major trauma, or when kidneys more susceptible to damage e.g. PKD, hydronephrosis
Grade from I to V, from contusion up to laceration + shattered kidney
Most conservative treatment, if penetrating renal trauma need exploration and control vascular, debride, remove haematoma + mattress suture over absorbable material

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10
Q

Ureteric injury?

A

Iatrogenic, blunt abdo/pelvic trauma, penetrating usually gunshot, deceleration (PUJ shear), obstruction, fistula formation, ischaemic strictures post-hysterectomy
Cause pain, infection, functional issues
Repair includes debridement of necrotic tissue, mucosa-mucosa anastomosis, drains

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11
Q

Bladder trauma?

A

Blunt/penetrating, iatrogenic (TURBT), extra or intra-peritoneal
May see bruising, visible wounds, abdo distention, peritoneum, anuria, raised urea + creatinine
Extra-peritoneal - conservative, catheter drainage; intraperitoneal - open repair, AB, catheter

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12
Q

Urethral trauma?

A

Usually male.
Anterior - bulbar/penile urethra, mobile, injury by direct or penetrating trauma
Posterior - membranous/prostatic urethra, find by puboprostatic ligament
Symptoms - difficulty voiding, high riding prostate. butterfly bruise if Buck’s fascia ruptures
Risk of incontinence, strictures and impotence
Suprapubic catheterisation

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13
Q

Penile trauma?

A

Penile # - strong bending force on erect penis, sudden pain tearing + detumescence. Due to tear in tunica of corporal body, need surgery obv
Avulsion/degloving
Ischaemia
Amputation - assault, psychiatric illness

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14
Q

Scrotal trauma?

A

Penetrating, blunt, avulsion

Pain, oedema, may not be able to palpate (?rupture)

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15
Q

What are the complications of urinary obstruction?

A
  • Proximal distention of UT - bladder dilatation + hypertrophy + diverticulae, in ureter - megaureter + hydronephrosis
  • Pain
  • Reduced renal function - back pressure causing tubular atrophy, glomerular hyalinisation + fibrosis
  • Urinary stasis - UTI, sepsis, stones
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16
Q

What are the commonest sites of urinary obstruction?

A

Pelvi-Ureteric junction (ureters cross brim at level of iliac vessels)
Vesico-ureteric junction (where joins bladder)

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17
Q

Causes of urinary obstruction?

A
  • Within lumen - clot, calculi, sloughed papillae, tumour of renal pelvis/ureter
  • Within wall - strictures of ureter/urethra, congenital megaureter, bladder neck obstruction, neurogenic bladder
  • Pressure from outside: PUJ compression, prostate cancer/BPH, retroperitoneal fibrosis, pancreatitis, Crohn’s disease, chronic granulomatous disease, phimosis
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18
Q

How may urinary obstruction present?

A
  • Acute UT obstruction - flank pain, radiates to IF/inguinal/genital/back, provoked by alcohol/high fluid/diuretics, occasionally enlarged kidney, symptoms of UTI/sepsis, N&V, anuria
  • Chronic UT obstruction - pain, CKD, polyuria
  • Acute LT obstruction - severe suprapubic pain (but absent in acute on chronic/neuropathy), abdo distention, suprapubic dullness
  • Chronic LT obstruction - urinary symptoms, signs f prostate issues
  • Idiopathic retroperitoneal fibrosis - uncommon, non-specific dull ado-low back pain, 50% have HTN, anaemia, raised CRP/ESR. Around half due to metastasised cancer, causes hydronephrosis, IVCO. Steroids + stents
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19
Q

Complications of urinary obstruction?

A
Infection - cystitis, pyelonephritis, abscess, sepsis
Urinary extravasation
AKI
Fistula
CKD
Bladder dysfunction
Pain
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20
Q

Ureteric colic?

A

C-calculi, clot, PUJ obstruction
CF-sudden onset colicky pain, radiation to IF/genitals, u/l, N&V, may have rigors/tachycardia/hypotensive (sepsis), non-visible haematuria
M-analgesia, anti-emetic, fluids if dehydrated, many pass spontaneously, IV ABs if have infection (gentamicin + co-amox/tazocin), drainage of abscess, surgical removal of stone

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21
Q

Acute pyelonephritis

A

Causes: E coli, Proteus miribalis (forms stag horn calculi by urinary alkalisation due to urease), Pseudomonas, Klebsiella …
CF: pain may be more gradual onset, not colicky, radiates, often preceding UTI, systemically unwell, pyrexial, tender flank/suprapubic, dysuria, strong smelling cloudy urine, haematuria, pyrexia, tachycardia, urine dip often blood leucocytes + nitrates
M: medical, analgesia, anti-emetic
C: pyonephrosis, perinephric abscess (gets into fat, slowly expanding loin mass, need drainage usually), sepsis

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22
Q

What part of the prostate is palpable on DRE?

A

Posterior part, feel median groove which divides the two lateral lobes

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23
Q

What is benign prostatic hyperplasia?

A

Transition zone undergoes nodular hyperplasia - symmetrical enlargement - can cause bladder outflow obstruction, back pressure, overflow incontinence, urinary sx

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24
Q

How is BPH managed?

A
  • Cystoscopy for assessment
  • Finasteride/dutaseride - 5 alpha reductase blockers. Reduce conversion of testosterone to dihydrotestosterone so reduce hyperplasia, takes 6m to work, s/e are erectile dysfunction, reduced libido, gynaecomastia
  • Alpha A1 blockers e.g. tamsulosin, alfuzosin - allow prostatic urethra to open more readily, s/e are postural hypotension, dry mouth, depression
  • TURP - remove most of prostate in strip. Comps-retrograde ejaculation, impotence, urethral strictures, clot retention from secondary haemorrhage (infection or cancer)
  • Long-term catheterisation - small proportion. Intermittent self-catheterisation best as reduces infection
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25
Q

Prostate cancer presentation?

A
  • Starts peripherally so urinary symptoms usually a later feature - often asymptomatic. Other symptoms include oedema of legs/genitals from nodal involvement, backache, pathological #.
  • Most adenocarcinomas and well-differentiated.
  • Highest prevalence in Afro-Caribbean men
  • Metastasise to pelvic and obturator LN, seminal vesicles, bone (esp via sub scapular venous plexus into spinal veins)
  • Most secrete prostate specific antigen - but this also raised in BPH, prostatitis
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26
Q

Prostate cancer grading

A

TRUS biopsies, serum PSA, XR for bone pain (typically sclerotic [osteoblastic, dense, white] rather than lytic lesions)

Gleason score
Get grade 1-5 for most dominant and second most dominant, add the two scores together so out of 10
Lowest Gleason score indicating malignancy is 6/10.

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27
Q

Management of prostate cancer

A

Early: prostatectomy, +/- radiotherapy often curative, or active monitoring if low grade + impalpable

Hormonal treatments - most tumours androgen dependent . E.g. goserelin (LHRH agonist so stimulates LH release from AP, increases testicular testosterone initially then this feeds back to inhibit LH release)
Also give anti-androgen treatment e.g. cyproterone acetate or flutamide initially due to risk of tumour flare from initial stimulation of testosterone + LH (which causes symptoms)

Locally-advanced-neoadjuvant radiotherapy + surgery

Metastatic: control sx,reduce progression

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28
Q

TURP syndrome?

A

Rare serious complication of prostate surgery, caused by venous destruction + absorption of the irrigation fluid.
RF: surgery >1h, large amount of fluid used, poorly controlled CCF, large blood loss, perforation

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29
Q

Prostatitis

A
  • Usually coliforms, Chlamydia or Gonorrhoea or Neisseria
  • Acute: perineal pain, fever, swelling, obstruction, tender prostate. IV AB to reduce fever then PO for 6w
  • Chronic: low grade suprapubic/perineal pain, vague symptoms, ABs and NSAID
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30
Q

When should you not do PSA test within due to risk of increased result? (NICE)

A
6 weeks of a prostate biopsy
4 weeks following a proven urinary infection
1 week of digital rectal examination
48 hours of vigorous exercise
48 hours of ejaculation
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31
Q

Urological tumours?

A

Renal cell adenocarcinoma - mostly sporadic but ass w von Hippel-Lindau syndrome, smoking. Involves large clear cells, can invade para-aortic LN, renal vein, IVC, lung (cannonball mets), liver, bone. CF-haematuria, mass, flank pain, often incidental. Less common-iron def anaemia, polycythaemia (EPO), HTN (renin), hypercalcaemia (PTHrP), PUO, varicocele on L from obstruction of LTV. M-nephrectomy, isolated pulmonary met removal may cure

Nephroblastoma - Wilms’ tumours. Developmental, mass + haematuria, pyrexia, often met early to lung

Benign renal tumours - oncocytoma, adenoma, angiomyolipoma (ass w tuberous sclerosis)

Transitional cell carcinoma - anywhere in UT but mostly bladder, 4x more common than RCC, RF-smoking, industrial carcinogens (long incubation) Carcinoma in situ-frequency + dysuria. CF-painless haematuria, v occasionally clots causing UT obstruction, hydronephrosis if near ureteric orifice. M-single dose intravesical chemotherapy, TURBT, cystectomy with urinary diversion via ideal conduit

Squamous cell carcinoma - ass w stones/schistosomiasis

Adenocarcinoma of bladder - v rare, remnants of urachus

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32
Q

Pathophysiology of renal stones

A

Supersaturation when concentration of minerals exceed their solubility in urine. Most include calcium with the commonest being calcium-oxalate
Calcium-containing usually idiopathic or hypercalcaemia
Excess urinary excretion of main component can cause- hyperparathyroidism (calcium), hyperoxaluria (oxalate), gout/chemotherapy (uric acid), cysteinuria (metabolic disorders), struvite stone (infection-alkaline urine from urease-producing enzymes)

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33
Q

What is a struvite stone?

A

Form majority of stag horn calculi, made of ammonium, magnesium + phosphate
Proteus miribalis - produces urease-producing enzymes - alkalinises urine - these stones form in the renal pelvis

34
Q

Presentation of urinary stones

A
  • Most asymptomatic
  • Pelvicalyceal obstruction - pain, hydronephrosis, renal impairment
  • Ureter - may pass if go into bladder with minor symptoms, if large obstruction/retention, impaction (severe pain, colicky, due to ureteric peristalsis)
  • UTIs due to stasis + areas for bacteria to multiply
  • Local damage/irritation - haematuria, chronic fibrosis, strictures, SCC
35
Q

What is the investigation of choice for renal stones?

A

CT KUB, non-contrast (most are radio-opaque cos of the calcium)

Peri-ureteric fat stranding may indicate recent stone passing, or pyelonephritis

IV urography - sometimes done but not as good as CT tbh, only if they don’t have CT

US for hydronephrosis (acutely)

36
Q

Management of acute renal stones

A
  • IM diclofenac, longer lasting + not addictive, usually settles after 1-2 doses. oral if less pain
  • Morphine - avoid as tends to prolong ureteric spasm
  • Percutaneous nephrostomy - if complete obstruction
  • Surgery if infected to avoid sepsis
  • Alpha adrenergic blockers aid passage
  • Treat cause e.g. hyperuricaemia – allopurinol
37
Q

What organisms tend to cause UTIs?

A

Faecal bacteria like E coli, Proteus, Enterococcus faecalis
Catheterised - Pseudomonas
Young sexually active women - Staph saprophyticus

38
Q

Lower UTI?

A

Infection of bladder
Urinary symptoms, lower abdo pain, may have no localising symptoms except enuresis or incontinence
Don’t need dipstick. MSU if unsure/recurrent
M: trimethoprim or nitrofurantoin for 3d in women, 7d in men. Drink lots, wipe F to B, empty bladder post-intercourse, frequent complete bladder emptying, correct other issues like constipation/catheters

39
Q

Other urinary tract infections

A
  • Genitourinary TB - caseating granulomas that calcify, can cause ureter/bladder strictures, often asymptomatic
  • Schistosomiasis - parasitic infection - CI, fibrosis, stones + SCC. Tropical, infected by bathing in contaminated water - penetrate skin - go through venous circ + lungs to arterial circ - disseminate - worms mate in portal veins - get through mesenteric veins to pelvic viscera. Causes rash at site of penetration, low grade illness, eosinophilia, frequency, terminal haematuria. M-praziquantel
  • Urethral infections with gonorrhoea and chlamydia - discharge and dysuria
  • Urethral strictures - iatrogenic in TURP, catheterisation in poor tissue perfusion. Progressive decline in stream
40
Q

Congenital urological conditions (majority present as child/birth, except PKD)

A
  • Polycystic kidneys - presents in adults, autosomal dominant. B/l multiple cysts, slowly expand + compress. HTN, CKD, pain, vulnerable to trauma. Some also get cysts in liver + pancreas, half need dialysis/transplant
  • Medullary sponge kidney - cyst like dilatation of renal medulla CD, predisposes to infection/stones
  • Duplex systems - duplicates of part of urinary tract, may cause damage from infection/reflux/obstruction
  • Renal cysts-usually asymptomatic
  • Horseshoe kidney - embryological fusion of kidneys at lower poles so can’t ascend properly due to IMA so lies around aorta at L3-4, usually no symptoms
  • Ectopic kidneys
  • U/l agenesis/aplasia/hyperplasia
  • Urachal abnormalities - e.g. fistula between bladder and umbilicus
41
Q

Testicular torsion (of spermatic cord)

A

Younger patients, sudden onset u/l pain, radiate to groin/IF/flank, N&V, often no UTS, apyrexial, tachycardic, normotensive, erythematous, may have transverse lie of opposite side, if can’t feel scrotum may be due to oedema
Needs emergency exploration +/- orchidectomy
In torsion of testicular appendage cremasteric reflex usually preserved, in torsion of spermatic cord usually absent
C: infarction, gangrene

42
Q

Acute epididymitis

A

Usually due to urethral infection ascending through vas deferens (UTI in 50-65s, or STI in 15-30s)
Acute pain, oedema, erythema, warmth, hard to palpate epididymis from testis
M: long course of ABs, pain relief
C: Fournier’s gangrene (necrotic area of scrotal skin, high mortality)

43
Q

Torsion of hyatid of Morgagni (testicular appendage)

A

Doesn’t affect function, cremasteric reflex usually preserved
Usually in children, sudden onset u/l scrotal pain, testis hangs normally, tender at upper pole, minimal oedema, surgery to rule out torsion

44
Q

Non-torsion or epididymitis causes of testicular pain?

A

Haematocele post-surgery eg vasectomy
Tumours
Trauma - usually blunt + part of multiple trauma
Ureteric calculi
Chronic scrotal pain from inflammation, often traced to a vasectomy. E.g. Chronic bacterial epididymitis

45
Q

What may cause a scrotal swelling?

A
  • Indirect inguinal hernia - no translumination, cannot palpate above it (can’t feel superior border)
  • Diffuse enlargement with small secondary hydrocele - assume malignant
  • Focal enlargement - assume malignant
  • Epididymal cysts
  • Spermatocele
  • Chronic epididymitis
  • Hydrocele
  • Fournier’s scortal gangrene
  • Haematocele
  • Varicocoele
  • Granulomatous *infection
  • Lymphoma
  • Epididymitis
  • Orchitis
  • Tumours
46
Q

Cysts derived from epididymal tissue?

A

Epididymal cysts - painless swelling, can palpate testis separately, transluminates
Spermatocoele - less common, cyst contains spermatozoa, usually at head of epididymis, may or may not transluminate

47
Q

Hydrocoeles?

A

Primary - abnormal collection of fluid in tunica vaginalis. In children may be communication with peritoneal cavity from patent processus vaginalis, or non-communicating due to impaired reabsorption of serous fluid. Soft and non-tender, can’t usually palpate testis, transilluminates, can get above it
Secondary - irt tumour or inflammation, most small
Hydrocele of the cord - rare, in remnant of PV, transluminates, in females can get groin swelling due to hydrocele of canal of Nuck (degeneration of round ligament)

48
Q

What is Fournier’s scrotal gangrene?

A

Necrotising fasciitis of genitalia + perineum, NOT TESTIS. often due to anaerobic infection

Often septic

Causes: primary hydrocele, trauma, perirectal abscess, urethral strictures

RF - DM, steroids, chemotherapy, alcohol abuse

M: urgent IV ABx, surgical excision, leave wound open to heal by secondary intention

49
Q

Haematocele?

A

Presents like a hydrocele post-trauma, doesn’t;t transluminate

50
Q

Varicocele?

A

Dilatation of pampiniform plexus of spermatic cord - scrotal swelling separate from testis + epididymis, feels like ‘bag of worms’, disappears on lying down as distended veins collapse

90% on left - LTV drains into renal vein (higher pressure)

Usually asymptomatic. Increase scrotal temperature so inhibits sperm function. Rare cause RCC obstruction of L RV, these do not collapse when lying down

Surgery for pain relief or in children/young adults to preserve spermatogenesis (usually percutaneous embolisation)

51
Q

Orchitis?

A

Primary bacterial is rare
Tertiary gummatous syphilis - diffuse non tender enlargement
Viral - mumps, if b/l causes infertility in half, 4-6d after parotitis with extreme tenderness + inflammatory hydrocele

52
Q

TB epididymitis

A

Thickened non-tender epididymis, ‘cold’, diagnose with early morning urine sample for mycobacteria

53
Q

Where do testicular tumours metastasise to?

A

Para-iliac and para-aortic LNs around L1-2 (whereas scrotal go via skin to inguinal nodes), then thoracic duct, supraclavicular nodes + systemic circ, or in blood to lung

Seminomas tend to spread via lymph
Teratomas tend to spread via blood to lungs

54
Q

Risk factors for testicular cancer?

A

Cryptorchidism (absent scrotal testis), infertility, FH, Klinefelter’s syndrome, mumps orchitis

55
Q

Presentation of testicular cancer?

A

Painless swelling of testis, secondary hydrocele from involvement of testicular capsule, gynaecomastia (beta-hCG release), may have hard mass, heavy dragging feeling

Examine - see if arises in groin/spermatic cord/scrotum (in a hernia the cord is broader than normal). Try to palpate testis + epididymis separately, tiny focal lumps in epididymis usually fine, infection may cause thickened epididymis, epididymal cysts usually at upper pole + transilluminate

Do USS testes, CXR (lung mets), routine bloods + tumour markers (at presentation, after starting treatment + during FU; ensure alpha feta-protein, hCG, LDH)

Management - radical inguinal orchidectomy - removes testis + spermatic cord, to reduce spreading risk. Chemo.

56
Q

Types of testicular tumours

A
  1. Germ cell tumours - majority
    Seminomas-pale, creamy white homogenous inside, peak age 35, type called spermatocytic seminoma in older which almost never mets. Normally AFP + HCG normal
    Non-seminomas e.g. teratoma - worse prognosis, peak incidence 25, from multipotent cells so can have all tissue types, usually raised AFP + hCG
  2. Sex cord/gonadal stromal tumours - Leydig cell, Sertoli cell or mixed
  3. Misc - lymphoma, leukaemia, tumours of CD and rete testis
57
Q

Testicular tumour markers

A

beta-hCG: released by syncytiotrophoblast cells, esp poorly-diff germ cell tumours
Alpha-fetoprotein - yolk sac tumours, most teratomas
LDH - elevated in most with metastatic seminoma
High ALP - tumours with seminoma component
High hCG - teratomas with trophoblastic (choriocarcinomatos) components

58
Q

Urological causes of abdo pain

A
  • Upper tract: stones, tumours, polycystic disease, pyelonephritis, acute obstruction (colicky pain), infection
  • Lower tract (suprapubic pain): cystitis (may refer to penis/vulva if the trigone is involved), prostatitis (usually felt deep in perineum)
  • Non-urological but same area: MSK, gynae, gen surgical causes, vascular (dissecting iliac aneurysm)
59
Q

Acute loin pain causes

A

RENAL:

  • renal colic: sudden onset, severe, may radiate anteriorly/to groin, tender over renal angle, 85% a/w haematuria
  • pyelonephritis: pt unwell, dull ache, likely leucocytosis + pyuria
  • blood clots causing sudden ureteric obstruction, may be due to a bleeding disorder or renal biopsy
  • papillary necrosis: acute obstructed ureter from sloughed papilla e.g. analgesic abuse, cirrhosis, recurrent pyelonephritis
  • kidney tumours: gradual onset, may be painless haematuria
  • PUJ obstruction: usually from drinking lots of fluid-diuresis causes distension of renal pelvis
  • renal infarction

OTHER LOCAL CAUSES:

  • dissecting AAA
  • herpes zoster, muscular pain
  • injury
  • retroperitoneal fibrosis: dull, insidious onset, can affect ureters causing hydronephrosis
  • less common: IBD, appendicitis, renal vein thrombosis, glomerulonephritis, splenic infarct
60
Q

Post-obstructive diuresis

A

Prolonged urine production following relief of urinary retention/obstructive uropathy – potentially life-threatening polyuria (shock, low K/low or high Na/low Mg). Basically because the obstructed state became less sensitive to ADH

Management: replace electrolytes + volume. lasts around 48hr

61
Q

What are the types of urinary incontinence?

A
  • Stress
  • Urge
  • Mixed
  • Functional - delirium, dementia, immobility, UTI, etc etc
  • Secondary to prostate problems
62
Q

What Ix are done for urinary incontinene?

A
  • encourage voiding diary
  • urinalysis + culture (infection, DM)
  • bladder scan: measures post-void residual volume, high RV indicates bladder atony/obstructed outlet
  • urodynamics: evaluates pressure-flow relationship between bladder + urethra
  • cystoscopy: if having irritative voiding sx/haematuria etc
63
Q

Outline the mechanism for voiding

A

Normal capacity 350-500ml, during filling detrusor muscle relaxes so pressure doesn’t rise until bladder capacity is approached, then detrusor contracts to void (both mediated by spinal reflex at S2-4). Also have cortical conscious control inhibitory mechanism to delay voiding – develops during early childhood.

64
Q

How is AKI managed?

A

o Treat cause
o Stop nephrotoxic drugs where possible
o Monitor U+Es, glucose (as hypoglycaemia is a risk)
o Identify and treat infection
o Fluid resuscitation but avoid fluid overload (need accurate measurement of urine output)
o Urgently relieve any obstruction
o Referral for RRT if hyperkalaemia/pulmonary oedema/severe metabolic acidosis/progressive failure/uraemic complications [pericarditis, uraemic encephalopathy]/renal transplant/CKD stage 4 or 5

65
Q

Causes of AKI

A
  • pre-renal: volume depletion (haemorrhage, severe D+V, etc), oedema (eg nephrotic syndrome, cirrhosis), hypotension (shock), renal hypo perfusion (hepatorenal syndrome, NSAIDs, ACEi/ARBs, renal artery stenosis)
  • renal: glomerular (glomerulonephritis, thrombosis, haemolytic uraemia syndrome), tubular (ATN from ischaemia, nephrotoxins, light chains in myeloma), acute interstitial nephritis (NSAIDs, infection, autoimmune), vascular disease (polyarteritis nods, renal artery stenosis, renal vein thrombosis), eclampsia
  • post-renal: stones, clot, papillary necrosis, urethral stricture, BPH/Ca prostate, radiation fibrosis, pelvic tumour, retroperitoneal fibrosis
66
Q

CF of AKI

A

NICE: reduced urine volume <0.5ml/kg/hr for >6hr, rise in serum creatinine of 26 um/L or more over 48hr, 50% or greater rise in serum creatinine within preceding 7d

Sx: reduced UO (or PO from reduced fluid absorption if there is damaged tubules), acute anuria (obstruction), gradual reduction (BPH, strictures etc), N+V, dehydration, confusion

Signs: HTN, signs of chronic retention ie large painless bladder, dehydration, fluid overload, signs of vascular disease

67
Q

How is urinary obstruction managed?

A
  • partial obstruction without infection or renal impairment - analgesia + hydratio
  • complete obstruction - catheterise ASAP, may need stenting of ureter or a nephrostomy
  • stones: <5mm usually pass, >10mm need intervention, in between depends on sx. Usually pain <72h, give diclofenac IM/PR first line, fluids. Larger stones may try alpha blockers to expel/lithotripsy
  • PUJ obstruction needs surgery
  • Malignancy - ureteric stent, percutaneous nephrostomy
  • Retroperitoneal fibrosis - biopsy to r/o cancer, usually needs a stent or ureterolysis
  • BPH - catheter, reduce fluids + avoid caffiene/alcohol, alpha blockers + 5-alpha reductase inhibitors, surgery less frequently done now
  • post-urethral trauma - suprapubic catheter to allow healing
68
Q

What factors contribute to the development of renal stones?

A

urine stasis esp w infection (hydronephrosis, chronic obstruction e.g. BPH), chronic urinary infection (e.g. Proteus – cause alkaline urine and development of staghorn calculi of renal pelvis – these are struvite, made up of ammonium, magnesium and phosphate – urinary alkalinisation from urease-producing enzymes from Proteus miribalis infection), excess urinary excretion of stone-forming substances, foreign bodies (e.g. parasites), dietary (excess dairy, high Ca2+ in water)

69
Q

Retroperitoneal fibrosis

A

progressive fibrosis of CT posterior to peritoneal cavity, around half due to retroperitoneal spread of cancer. Compresses both ureters causing b/l hydronephrosis and renal failure, can cause IVC obstruction. Treatment w steroids and stents to maintain upper tract function

70
Q

Phimosis

A

foreskin too tight to be retracted due to a fibrotic ring - can cause urinary obstruction, haematuria, painful erection, local pain, chronic infection

do not forcibly retract (can cause scarring), personal hygiene, if >2y may need surgery, can try steroid cream

is a RF for penile carcinoma

71
Q

Paraphimosis

A

tight prepuce is retracted then can’t be replaced as the glans swells + impedes venous return - urological emergency. Ensure no constricting foreign body.

RF: vigorous sexual activity, penile piercing, catheterisation, failing to pull foreskin forward to natural period after cleaning etc – as it causes swelling

CF: pain on erection, oedema, necrosis

M: gentile compression with saline soaked swab then reduction of prepuce over the glans (obv with LA/entonox). circumcision when oedema reduced

72
Q

Balanitis

A

inflammation of the glans penis, if foreskin also inflamed correct term is balanoposthitis but commonly just referred to as balanitis

adults>children

RF: DM, oral Abx, poor hygiene, immunosuppression, physical/chemical irritation

various organisms cause it including bacteria, candida, derm causes (e.g. sulphonamide drug eruption), balantitis xerotica obliterans, irritation from soaps, morbid obesity, zip irritation etc etc etc

CF: red inflamed painful, penile ulceration, purulent/foul smelling discharge, dysuria, interference with urinary flow, regional lymphadenopathy

Ix: swab discharge for MCS, blood/urine test for DM, rule out STI

M: clean with warm water/saline, dry by air, treat+screen for STI, adv derm/urology as appropriate, usually use topical steroids, avoid triggers, candida-clotrimazole cream/oral fluconazole, bacterial-fluclox/erythromycin

73
Q

Testicular maldescent

A

testis start descent normally but arrest in the inguinal region (or less commonly still in abdomen). Risk higher in prematurity.

Issues: neoplasia (risk reduced when do surgery early, usually seminomas, ensure regular self checks), subfertility (incomplete maturation of seminiferous tubules so abnormal sperm), torsion (abnormal mobility), psychological

optimally do orchidopexy at 6-12 months (mobilise testis + spermatic cord via a groin incision)

74
Q

Vesicoureteric reflux

A

commonest reason children get recurrent UTIs. Retrograde flow of urine from bladder to kidneys due to faulty mechanism at junction of ureter and bladder. Causes include posterior urethral valves, detrusor instability and congenital megaureters.

75
Q

Pelviureteric junction dysfunction

A

can present from birth – 30s. Causes hydronephrosis, usually due to aperistalsis. May lead to stones, recurrent infection, progressive renal impairment.

76
Q

Hypospadias

A

common congenital abnormality of penis + urethra causing meatus to be along ventral surface of urethra, and urethral remnant distant to this is fibrotic. Penis often bends down/sideways on erection – chordee. Specialised surgery, never do circumcision as foreskin is needed for the surgery

77
Q

Epispadias

A

rare. Urethral meatus on dorsal aspect of penis

78
Q

Posterior urethral valves

A

congenital mucosal folds that impede/occlude urinary flow. Causes obstruction

79
Q

Male erectile dysfunction (prev-impotence) causes

A

Inability to attain + maintain an erection sufficient for sexual function, big impact on QoL

RF: age, obesity, smoking, HTN, DM

Causes:

  • vascular: atherosclerosis, HTN, DM, smoking, surgery/radiotherapy to pelvic area
  • central neuro: PD, stroke, MS, tumours, traumatic brain injury (HP dysfunction), IV disc or SC disease/injury
  • peripheral neuro: polyneuropathy, peripheral neuropathy, DM, alcoholism, uraemia, surgery
  • hormonal: hypogonadism, hyperprolactinaemia, thyroid disease, Cushing’s disease
  • anatomical: Peyronie’s disease (asymmetrical fibrosis of fascia in CC causing penis to bend), “micropenis”
  • drugs: antihypertensives, BB, diuretics, TCA/SSRIs, antipsychotics (risperidone), antihistamines, recreational drugs, H2RAs
  • psychosexual: general, situation (e.g. stress, partner)
  • psychiatric illness: depression, anxiety, alcoholism
80
Q

Male factor infertility causes

A
  • general health issues like obesity, smoking, tight underwear, anabolic steroids, alcohol, other drugs
  • disorders of testis/spermatogenesis: persistent azoospermia, genetic things (Klinefelter’s, Kallman syndrome, testicular virilisation), cryptorchidism, varicocele, testicular tumours, trauma, pituitary causes (tumours, severe hyperprolactinaemia, Simmond’s disease, Cushing’s disease)
  • disorders of genital tract
  • ejaculatory disorders e.g. retrograde ejaculation
  • idiopathic - 40%
81
Q

Priapism

A

This is abnormally prolonged penile erection lasting 4h or more. Usually painful, doesn’t need sexual stimulation and doesn’t resovle after ejaculation. Only affects corpora cavernosa. Can be high flow (arterial, less painful, associated with trauma, uncommon) or venous (due to occlusion of venous outflow leading to penile ischaemia, v painful, if untreated leads to fibrosis + impotence). Commonest cause is side-effect of injected intracavernosal drugs used for erectile dysfunction. Treatment of venous occlusive priapism needs to be prompt – ice packs, aspiration of blood using butterfly needle, intracavernosous injection of alpha agonists )phenylephrine) or PO terbutaline (beta agonist).

82
Q

How may you differentiate the causes of erectile dysfunction?

A

Organic causes - suggested by gradual onset, normal ejaculation + libido, risk factor in PMH, smoking/high alcohol

Psychogenic causes - suggested by sudden onset, early collapse, waking erections, premature/failure to ejaculate, problems in relationship, major life events, psychological problems