Surgery - Urology Flashcards

1
Q

What is the pathophysiology of renal stones, what are they made of?

A
  • Can be renal stones or ureteric stones
  • 80% are calcium (calcium oxolate, calcium phosphate, mixed oxolate and phosphate)
    • The rest are struvite (staghorn calculi), urate (radiolucent) and cystine

Stones usually impact in narrowed points

  • Pelviureteric Junction
  • Crossing pelvic brin where iliac vessels travel across ureter
  • Vesicoureteric Junction

Causes

  • Urate stones = High purine (lots of red meat diet or myeloproliferative disease)
  • Cystine stones = homocystinuria
  • Oversaturation of urine basically causes the majority of them
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2
Q

How do renal tract calculi present?

A
  • Sudden onset severe pain radiating from flank to pelvis
  • Nausea and vomiting
  • Haematuria (typically microscopic)
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3
Q

How would you investigate for renal tract calculi?

A
  • Urine dip for haematuria and infection (send urine culture too)
  • Routine bloods
    • U&es for kidney function
    • Urate and calcium levels too
  • Gold standard = Non contrast CT of Renal tract (CTKUB)
  • AXR sometimes however not all stones are radio-opaque
  • USKUB for hydronephrosis if u&es deranged
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4
Q

How would you manage renal tract calculi?

A
  • Fluid resus as they are usually dehydrated
  • If lower ureter or <5mm diameter = usually pass on their own with sufficient analgesia
    • Opiate analgesia and NSAIDs per rectum are most effective
  • >5mm stone or infected stone requires hospital admission
  • Obstructive nephropathy or significant infection = retrograde stent insertion or nephrostomy
    • These are temporary measures
    • You need to relieve the obstruction immediately to avoid kidney damage
  • For stones that do not pass spontaneously
    • Extracorporeal Shock Wave lithotripsy
      • For smaller ie <2cm stones
    • Percutaneous nephrolithotomy
      • For renal stones only
      • Preferred for large stones eg. staghorn calculi
    • Flexible uretero-renosocpy

Recurrent stones

  • Tell patients to stay hydrated
  • Oxolate = avoid high purine foods and high oxolate foods (nuts, rhubarb, sesame)
  • Calcium = check pth to exclude primary hyperparathyroidism, avoid excess salt
  • Urate = avoid high purine foods (red meat, shellfish), give purine lowering meds (allopurinol)
  • Cystine = genetic testing
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5
Q

What are bladder stones?

A
  • Form from urine stasis in the bladder so commonly seen in chronic urinary retention
  • Also occur secondary to infections like schistosomiasis
  • Present with LUTS
  • Manage with cystoscopy or fragment them with lithotripsy
  • Chronic irritation from bladder stones can cause SCC
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6
Q

What is pyelonephritis?

A
  • Inflammation of the kidney parenchyma and renal pelvis
    • Uncomplicated = normal urinary tract in a non-immunocompromised host
    • Complicated is the opposite
  • Common organisms
    • EColi, Klebsiella, Proteus, Enterococcus faecalis (catheter), S Aureus (catheters), Pseudomonas (catheters), Staph saprophyticus (commensal)
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7
Q

What are some risk factors of pyelonephritis? (think about individual risk factors)

A
  • Things that reduce antegrade flow of urine
    • Neuropathic bladder from spinal cord injury
    • Obstructed urinary tract eg bph
  • Things that promote retrograde ascent of bacteria
    • Female (short urethra)
    • Indwelling catheter etc
    • Structural abnormalities like vesico-ureteric reflux
  • Factors causing infection/immunocompromise
    • DM, corticosteroids, HIV
  • Factors causing bacterial colonisation
    • Renal calculi, sex, oestrogen depletion (menopause)
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8
Q

How does pyelonephritis present?

A
  • Triad = fever, unilateral loin pain, N&V
  • Perhaps also Lower UTI symptoms = dysuria, freq, urgency
  • Haematuria
  • o/e pyrexial, features of sepsis
    • unilateral or bilateral costovertebral angle tenderness +/- suprapubic tenderness
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9
Q

How would you investigate and manage pyelonephritis?

A
  • Urinalysis (nitrites and leucocytes) and send urine cultures
  • Urinary bhcg for women
  • Routine bloods
  • Renal Ultrasound scan (USKUB) to rule out obstruction
    • Pyonephrosis would be an emergency
    • If obstruction is suspected do a non contrast CTKUB

Management

  • A-e resus
  • Empirical antibiotics and iv fluids
  • Analgesia and anti-emetics
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10
Q

What kind of cancer is a renal cell carcinoma and what are some risk factors?

A
  • It is an adenocarcinoma of the renal cortex

Risk factors = smoking, industrial exposure to lead/aromatic hydrocarbons/cadmium, dialysis, HTN, obesity, polycystic kidney disease, horseshoe kidneys

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11
Q

How would RCC present?

A
  • Haematuria
  • Flank pain or flank mass
    • Left sided masses also present with left varicocele sometimes due to compression of left testicular vein as it joins left renal vein
  • Lethargy, weight loss etc
  • Paraneoplastic syndromes = polycythaemia (erythropoietin), hypercalcaemia (pth), HTN (renin)
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12
Q

How would you investigate and manage RCC?

A

Investigations

  • Routine bloods
  • Urinalysis and send for cytology
  • USKUB as routine for haematuria
  • CTCAP with iv contrast
  • TNM staging of cancer from renal biopsy

Management

  • Localised disease
    • Partial nephrectomy for small, radical nephrectomy for large
    • Unfit for surgery = Percutaneous radiofrequency ablation or lap/percutaneous cryotherapy
    • Surveillance
  • Mets disease
    • Nephrectomy + Immunotherapy
    • Biological agents like sunitinib or pazopanib
    • Metastasectomy if disease is resectable
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13
Q

What are renal cysts? How would you classify them?

A
  • Fluid filled sacs in the kidney
  • Cysts can be Simple or Complex and are classified using the Bosniak classification
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14
Q

What are some risk factors of kidney cysts?

A

Risk factors = old age, smoking, htn, male gender, genetics (polycystic kidney disease, tuberous sclerosis, von hippel-lindau disease)

  • ADPKD is a mutation of PKD1 and PKD2 genes resulting in multiple renal cysts forming. Also associated with berry aneurysm formation, mitral valve disease, liver cysts. Pt eventually develop end stage renal failure
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15
Q

How do renal cysts present?

A
  • Flank pain (if rupture of infection)
  • Haematuria
  • PKD = uncontrolled hypertension and a flank mass
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16
Q

How would you investigate and manage renal cysts?

A

Investigations

  • CT imaging with IV contrast
  • Bosniak scoring for risk of malignancy
  • Routine bloods like U&Es

Management

  • Asymptomatic simple cysts you just leave
  • Symptomatic simple cysts are manged with simple analgesia
    • If significant impact to pt = needle aspiration or cyst deroofing
  • Complex cysts = depends on their bosniak stage
    • Continued surveillance or surgical intervention eg. nephrectomy
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17
Q

Most of incontinence in Gynae…

How would you manage Stress and Urge incontinence?

A
  • Lifestyle = weight loss, reduce caffeine, avoid excessive fluids, smoking cessation

Conservative

  • Stress 1st line = pelvic floor muscle training for 3 months
    • 2nd line = duloxetine (SNRI)
  • Urge 1st line = bladder training for 6 weeks
    • 2nd line = antimuscarinics like oxybutynin
    • Mirabegron for older ladies

Surgical

  • Stress = tension free vagina tape, open colposuspension, artificial urinary sphincter, intramural bulking agents
  • Urge = botulinum toxin A injections, percutaneous sacral nerve stimulation, augmentation cystoplasty, urinary diversion via ileal conduit
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18
Q

What kind of cancer is bladder cancer? Risk factors?

A
  • Transitional Cell Carcinomas 80-90%
  • Squamous Cell Carcinomas, adenocarcinomas, sarcomas

Risk factors = smoking, old age, aromatic hydrocarbons (industrial dyes or rubbers), schistosomiasis infection (risk for SCC), previous pelvic radiation

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19
Q

How does bladder cancer present?

A
  • Painless haematuria
  • Recurrent UTIs or LUTS
  • Pelvic pain
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20
Q

How would you investigate and manage bladder cancer?

A

Investigations

  • TNM staging
  • Urgent cystoscopy (flexible cystoscopy under LA)
    • If suspicious lesion identified from initial cystoscopy then do a rigid cystoscopy under GA too
    • Do a biopsy on rigid cystoscopy
    • Also potentially do a Transurethral Resection of Bladder Tumour (TURBT) during rigid cystoscopy
  • CT staging
  • Urine cytology (not that sensitive though)

Management

  • Non muscle invasive bladder cancer
    • T1 = TURBT
    • If higher risk, give adjuvant intravesicle therapy eg. Mitoycin C or BCG (Macille Calmette-Guerin)
    • Radical Cystectomy can also be offered to high risk disease
    • Regular surveillance via cytology and cystoscopy due to high risk of recurrence
  • Muscle invasive bladder cancer
    • Radical cystectomy!!!
      • Neoaduvant chemotherapy (cisplatin combo regimen)
      • Need a urinary diversion following cystectomy through ileal conduit formation or bladder reconstruction
      • Monitor b12 and folate annually as ileum is resected in urinary diversion procedures
    • Regular follow up with CT imaging
  • Metastatic or locally advanced cancer
    • Chemotherapy
    • MDT team, palliative team
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21
Q

What is the first thing you would do if you had a scrotal lump?

A

1st line is ultrasound scan of scrotum

  • No biopsy needed even to rule out testicular cancer as it can risk seeding cancer
  • Do tumour markers = Lactate Dehydrogenase (LDH), Alpha-fetoprotein (AFP), B-hCG
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22
Q

What are 5 extratesticular causes of a scrotal lump and 4 testicular causes?

A

Extratesticular

  • hydrocoele
  • varicocoele
  • epididymal cysts (spermatocoele)
  • epididymitis
  • inguinal hernia

Testicular

  • testicular tumour
  • testicular torsion
  • benign lesions = leydig cell tumours, sertoli cell tumours, lipomas, fibromas
  • Orchitis
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23
Q

What is a hydrocoele? (brief)

A
  • Peritoneal fluid between parietal and visceral layers of tunica vaginalis
  • Painless fluctuant swelling that transilluminates
    • Large epididymal cysts also transilluminate
  • Can grow large and cause discomfort when sitting/walking
  • Can occur congenitally in neonates where they regress spontaneously
  • Can occur in infants due to patent processus vaginalis and need ligation
  • In older males need urgent US
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24
Q

What is a varicocoele? (brief)

A
  • Abnormal dilation of pampiniform venous plexus within spermatic cord
  • Feels like a bag of worms, there is a dragging sensation, disappears when lying flat
  • Typically on L side as spermatic vein drains into left renal vein (R drains into inferior vena cava)
  • Can cause infertility and testicular atrophy by increasing scrotal temp
    • Undergo semen analysis
  • Management = embolization or lap/open ligation of spermatic veins
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25
Q

What is a spermatocoele? (brief)

A
  • Benign fluid filled sacs arising from epididymis
  • Smooth fluctuant nodules that are above and separate from tests and transilluminate
  • Often there are multiple of them
  • Typically do not need treatment
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26
Q

What is Acute urinary retention and what are some risk factors?

A
  • New onset inability to pass urine (may be passing bits but still significant residual vol)
    • Results in pain and discomfort

Risks

  • Common in older male pt due to enlarged prostate eg. BPH, strictures or prostate cancer
  • Uti
  • Constipation
  • Severe pain
  • Meds like antimuscarinics, epidurals, spinal anaesthesia etc
  • Neuro causes like peripheral neuropathy, iatrogenic nerve damage in pelvic surgery, UMN disease (MS, parkinsons), Bladder Sphincter Dysinergy
27
Q

How does acute urinary retention present?

A
  • Acute suprapubic pain
  • Inability to micturate
  • Associated symptoms suggesting the cause eg. UTI, worsening voiding LUTS
  • O/E distended palpable bladder, suprapubic tenderness
  • PR to check for constipation or prostate enlargement
28
Q

How would you investigate and manage acute urinary retention?

A

Investigations

  • Post void bedside bladder scan for retained urine vol
  • Routine bloods
  • U&Es for high or low pressure
  • Urinalysis
  • US KUB if high pressured retention to check for hydronephrosis
    • High pressure retention = deranged renal function due to hydronephrosis
    • Low pressure retention is in patients where upper renal tract is unaffected due to competency of urethral valves or detrusor muscles contractility reduction/failure

Management

  • Immediate urethral catheterisation
    • Measure vol drained post catheterisation
    • Monitor urine output over 24 hours post catheterisation
    • Monitor for post-obstructive diuresis
  • High pressure urinary retention
    • Keep catheter insitu until definitive management is arranged (eg TURP) as repeated high pressure episodes can cause AKI and renal scarring and CKD
  • Otherwise can remove catheter in a TWOC 24-48 hours after insertion
    • If pt voids successfully with minimal residual vol = twoc successful
    • Multiple failed attempts warrant a long term catheter
  • Treat underlying cause eg. tamsulosin for bph
  • Check urinalysis for infection and give antibiotics etc
  • Review meds
29
Q

What is Chronic urinary retention and what are some risk factors?

A
  • Painless inability to pass urine
  • Typically long standing retention with significant bladder distension, resulting in bladder desensitisation (therefore minimal discomfort)

Risks

  • Most common cause is BPH, urethral strictures, prostate cancer
  • Women = pelvic prolapse, pelvic masses (fibroids)
  • Neuro = peripheral neuropathies, UMN (MS, Parkinson’s)
30
Q

How would chronic urinary retention present?

A
  • Painless urinary retention
  • Voiding LUTS eg. weak stream and hesitancy
  • Overflow incontinence (worse at night when sphincter tone is reduced = nocturnal enuresis)
  • Palpable distended bladder o/e with minimal tenderness
  • PR exam for prostate enlargement
31
Q

How would you investigate and manage chronic urinary retention?

A

Investigations

  • Post void bladder scan
  • Routine bloods
    • US KUB for high pressure if u&es deranged

Management

  • If >1L post void vol or high pressure retention = Long Term Catheter
    • Also monitor urine output for post obstructive diuresis
    • High pressure don’t undergo a twoc due to risk of repeated renal injury, therefore these pt need LTCs
  • An alternative to LTCs are intermittent self catheterisation
    • Pt needs to be taught how to self catheterise at regular intervals eg. 4-6 hours so needs good dexterity and compliance
32
Q

What is benign prostatic hyperplasia?

what are some risk factors?

A
  • Non cancerous hyperplasia of prostate tissue
  • Risk factors = old age, 1st degree fhx, African/Caribbean, obesity
33
Q

How would BPH present?

A
  • LUTS
    • Voiding = hesitancy, weak stream, terminal dribbling, incomplete emptying
    • Storage = urinary freq, nocturia, nocturnal enuresis, urge incontinence
    • Haematuria, haematospermia
  • DRE = smooth firm symmetrical prostate
34
Q

How would you investigate and manage BPH?

A

Investigations

  • International Prostate Symptom Score (IPSS) questionnaire
  • Urinalysis
  • Post void bladder scan
  • DRE and Prostate Specific Antigen
  • USKUB for prostate volume and hydronephrosis
    • Prostate >30ml is enlarged
  • Urodynamic studies

Management

  • Reassurance if it was incidental finding
  • Review their medications if they have LUTS
  • Tell them to keep a symptom diary
  • Lifestyle = moderate caffeine and alcohol
  • Medical
    • A-blockers like tamsulosin relax prostatic smooth muscle
      • Se = postural hypotension, retrograde ejaculation, floppy iris syndrome
    • 5a-reductase inhibitors like finasteride can be trialled too
      • They prevent conversion of testosterone to DHT so decrease prostatic vol
  • Surgical
    • Transurethral Resection of Prostate (TURP)
      • Endoscopic removal of obstructive prostate tissue using a diathermy loop
      • Complications = sexual dysfunction, retrograde ejaculation, urethral stricture, Turp Syndrome
      • TURP syndrome =
        • Turp involves use of hypoosmolar irrigation which can result in significant fluid overload and hyponatraemia as fluid is absorbed through exposed venous beds.
        • Patients present with confusion, nausea, agitation, visual changes
35
Q

What is prostatitis?

What are the risk factors for both acute and chronic?

A
  • Acute bacterial prostatitis is inflammation of the prostate gland
  • Typically due to ascending urethral infection
  • Common causes = E.Coli, Enterobacter, serratia, pseudomonas, proteus
    • Rarely stis like chlamydia or gonorrhoea
  • Chronic bacterial prostatitis is due to inadequately treated acute prostatitis

Risk factors for acute

  • Indwelling catheters, immunocompromise, phimosis or urethral strictures, recent surgery eg. TRUS biopsy, cystoscopy etc

Risk factors for chronic

  • Above + intraprostatic ductal reflux, neuroendocrine dysfunction, dysfunctional bladder
36
Q

How would prostatitis present?

A
  • Acute = LUTS, pyrexia, perineal/suprapubic pain, urethral discharge
  • DRE = tender boggy prostate
  • Inguinal Lymphadenopathy
  • Chronic = pelvic pain or discomfort for at least 3 months + LUTS
37
Q

How would you investigate and manage prostatitis?

A

Investigations

  • Urine culture
  • STI screen and routine bloods
  • Transrectal prostatic ultrasound to rule out prostate abscess

Management

  • Prolonged antibiotic treatment (quinolone) + analgesia
  • 2nd line especially for chronic = a-blocker or 5areductase inhibitors
  • Consider referral to chronic pain specialist
38
Q

What is epididymitis?

A
  • Inflammation of the epididymis (orchitis is inflammation of the testes)
    • Sometimes occur together = epididymo-orchitis
    • But mainly epididymitis on its own
    • Rarely orchitis on its own
  • Bimodal age distribution = 15-30 years old and >60 years old.

Causes in <35 year olds is typically sexual transmission = N.Gonorrhoea and C trachomatis

Causes in >35 year olds is typically enteric organism from a UTI = E Coli, Proteus spp, Klebsiella pneumoniae, Pseudomonas aeruginosa

39
Q

What are some risk factors for epididdymitis?

A
  • Non-enteric = MSM, multiple sexual partners, known gonorrhoea contact
  • Enteric = recent instrumentation or catheterisation, bladder outlet obstruction eg bph, immunocompromise
40
Q

How would epididymitis present?

A
  • Unilateral scrotal pain and swelling
  • Sometimes fever and rigors
  • O/E epididymis is tender on palpation, red and swollen
    • Cremasteric reflex intact
    • Prehns sign +ve (pain relieved on elevating scrotum)
41
Q

How would you investigate and manage epididymitis?

A

Investigations

  • Urine dipstick
    • If evidence for infection then send for urine microscopy and culture
  • First void urine for NAAT = n gonorrhoea, c trachomatis, m genitalium
    • And further STI screening if necessary
  • Routine bloods
  • Blood cultures if systemic infection
  • Ultrasound of testes with US doppler to confirm diagnosis
    • And rule out complications eg. testicular abscess
    • Epididymitis = increased vascularity of epididymis

Management

  • Antibiotics and analgesia
    • Enteric = ofloxacin 20mg PO BD for 14 days
    • STI = ceftriaxone** 500mg IM single dose and **Doxycycline 100mg PO BD for 10-14 days
  • Abstain from sexual activity until finished antibiotics done and symptoms gone
  • Education about barrier contraception
  • Orchidectomy for chronic epididymitis that does not improve with other therapy
42
Q

What is testicular torsion? What are some risk factors?

A
  • When spermatic cord and its contents twist within the tunica vaginalis, compromising blood supply to testicle
  • Testicle will infarct within hours!! Surgical emergency

Risk factors =

  • bell clapper deformity (horizontal lie to testes), 12-25 years old, previous testicular torsion, fhx of testicular torsion, undescended testes
43
Q

How would testicular torsion present?

A
  • Sudden onset severe unilateral testicular pain, sometimes referred to abdo
  • Nausea and vomiting
  • O/E high lying and horizontal lying testicle. Swollen and v tender
    • Cremasteric reflex is absent
    • Negative Prehns sign (positive in epididymoorchitis)
44
Q

How would you investigate and manage testicular torsion?

A

Investigations

  • Clinical diagnosis, take for scrotal exploration in theatre
  • Doppler Ultrasound
  • Urine dipstick

Management

  • Urgent surgical exploration to assess for torsion
    • If confirmed, do Bilateral orchidopexy
    • If testis are non-viable then do an orchidectomy
    • Risk of chronic pain, palpable suture, risk to fertility, etc.
  • Analgesia and antiemetics
45
Q

What is torsion of hydatid of Morgagni?

A
  • This is a remnant of the Mullerian duct that can become torted and present similarly
  • More common in younger ages.
  • Scrotum is usually less erythematous with a normal lie of testis.
  • Blue dot sign may be present in the upper half of the hemiscrotum = visible infarcted hydatid
46
Q

What is testicular cancer? What are the different types?

A
  • Most common in 20-40 years old
  • Classified into germ cell tumours (95%) and Non germ cell tumours
    • GCT can then be classified into seminomas and non-seminomatous GCT
    • GCT are normally malignant
    • NGCT are usually benign – typically Leydig cell or Sertoli cell tumours
47
Q

What are some risk factors for testicular cancer?

A

cryptorchidism, prev testicular malignancy, +ve fhx, kleinfelters syndrome

48
Q

How would testicular cancer present?

A
  • Painless unilateral testicular lump
    • Irregular, firm, fixed, does not transilluminate
  • Evidence of met seg. Weight loss, back pain, dyspnoea
49
Q

how would you investigate and manage testicular cancer?

A

Investigations

  • Tumour markers = BHCG, AFP, LDH
  • Scrotal ultrasound
  • CT contrast CAP
  • Do not do a trans-scrotal percutaneous biopsy!!! Causes seeding of cancer
  • Royal Marsden Classification for testicular cancer

Management

  • Main options are surgery, radiotherapy, chemo depending on tumour type and risk etc.
  • Surgery = inguinal radical orchidectomy
  • Do a pre fertility assessment, semen analysis and cryopreservation
  • NS GCT
    • Stage 1 = orchidectomy then potentially adjuvant chemotherapy if high risk
      • Surveillance with ct scan at 3 and 12 months
    • Mets NSGCT = chemotherapy
  • Seminomas
    • Stage 1 = orchidectomy and surveillance
      • Chemotherapy with high relapse risk
    • Mets = radiotherapy or chemotherapy
50
Q

What is forniers gangrene? What are some risk factors?

A
  • A form of necrotising fasciitis that affects the perineum
    • Rapidly spreading necrosis of subcutaneous tissue and fascia

Common organisms = Group A strep, C. perfringes, E Coli

Risk factors

  • DM, excess alcohol, poor nutritional state, steroid use, haematological malignancies, recent trauma to the region
51
Q

How does fourniers gangrene present?

A
  • Severe pain out of proportion to clinical signs
  • Pyrexia
  • As the disease progresses = crepitus, skin necrosis, haemorrhagic bullae, sensory loss of overlying skin
  • Patients deteriorate rapidly and become severely unwell –> septic shock
52
Q

How would you investigate and manage fourniers gangrene?

A

Investigations

  • Clinical diagnosis
  • Surgical exploration
  • Routine bloods and blood cultures
  • CT imagine
  • Laboratory Risk Indicator for necrotising fasciitis (LRINEC)

Management

  • Urgent surgical debridement asap
    • Partial or total orchidectomy
  • Broad spectrum antibiotics
  • Transfer to HDU
  • Fluid resus and close monitoring
53
Q

What is paraphimosis?

What are some risk factors?

A
  • Inability to pull forward a retracted foreskin over a glans penis
  • Glans becomes increasingly oedematous due to reduced venous return, resulting in vascular engorgement of distal penis and further oedema
  • Leads to penile ischaemia and worsening infection eg. Fourniers gangrene.

Risk factors

  • Phimosis, indwelling urethral catheter, poor hygiene, prior paraphimosis
54
Q

How would you manage paraphimosis?

A
  • Suitable analgesia eg. penile block via local anaesthetic
  • Reduction asap
    • If manual reduction** fails, then a **dorsal slit** or **emergency circumcision may be required
  • After reduction ensure definitive management like circumcision Is arranged as an outpatient
55
Q

What is priapism?

What are the 2 different types?

A
  • Unwanted painful erection lasting more than 4 hours

High flow (non-ischaemic) priapism

  • Arterial blood rapidly enters corpus cavernosum more quickly than it can be drained

Low flow (ischaemic) priapism

  • Blockage to the venous drainage of the corpus cavernosum = prolonged venous stasis results in ischaemia –> fibrosis –> impotence
56
Q

What are some causes of priapism (both ischaemic and non ischaemic)

A

Non ischaemic = penile or perineal trauma, spinal cord injury

Ischaemic =

  • iatrogenic = impotence drugs (like papaverine or alprostadil), antipsychotics, anticoagulants, antidepressants)
  • sickle cell disease
  • haematological disorders like leukaemia and thalassaemia
  • pelvic malignancy
57
Q

How would priapism present?

A
  • Ongoing and unwanted erection despite absence of sexual desires (>4 hours)
  • Ischaemic = painful and rigid erection
  • Non ischaemic = painless and not fully rigid erection
58
Q

How would you investigate and manage priapism?

A

Investigations

  • Corporeal blood gas to determine whether it is ischaemic or non ischaemic
  • Routine bloods + bone profile, haemoglobin electrophoresis (+/- drug screen)
  • Non ischaemic = assess for potential spinal injury

Management

  • 1st line = Corporeal aspiration
  • 2nd line = intracavernosal injection of a sympathomimetic agent like phenylephrine
  • 3rd line = surgical shunt to be inserted between corpus cavernosa and glans
    • Complications = erectile dysfunction
59
Q

What kind of cancer is penile cancer?

What are some risk factors?

A
  • Typically squamous cell carcinoma
    • Can also be basal cell, sarcomas, melanomas, urethral carcnomas

Risk factors

  • HPV (16,6,18), phimosis, smoking, lichen sclerosis, HIV infection (untreated), Psoralen-UV-A Photochemotherapy
  • Circumcision is deemed protective

Premalignant conditions = Condyloma acuminatum (genital warts), Bowens disease, Lichen Sclerosis

60
Q

How does penile cancer present?

A
  • A palpable or ulcerating lesion in the penis
    • Typically located on the glans
  • Lesions are painless, but can have discharge and bleeding
  • Inguinal lymphadenopathy
61
Q

How would you investigate and manage penile cancer?

A

Investigations

  • Refer to specialist regional centre for investigation
  • Penile biopsy to confirm diagnosis
  • Then try to confirm Inguinal lymphadenopathy via PET-CT
    • Then do CT CAP if inguinal lymphadenopathy is +ve to complete the staging
  • TNM staging is used

Management

  • Superficial non-invasive =
    • topical chemo like imiquimod or 5fluorouracil
      • Then repeated biopsy and long term surveillance
    • Or laser ablation or glans resurfacing
  • Most will need surgical treatment
    • Invasive but confined to glans =
      • local excision and partial glansectomy OR total glansectomy with reconstruction
      • Radical circumcision for just foreskin tumours
    • Invasive penile cancer =
      • Partial amputation with reconstruction OR total penectomy with perineal urethrostomy
        • radical neoadjuvant radiotherapy or chemo
    • If inguinal node involvement = radical inguinal lymphadenectomy + neo adj chemo or radio
  • Phallic reconstruction is possible
62
Q

What is a penile fracture? What would it look like?

A
  • Traumatic rupture of corpus cavernosa and tunica albuginea in an erect penis

Presentation

  • Hx of blunt trauma on erect penis
  • Popping sensation or a “snap” with immediate pain, swelling, detumescence
  • O/E penile swelling and discolouration (haematoma) = “aubergine sign”
    • Deviation away from lesion
    • Firm immobile haematoma can be palpated in the shaft = “rolling sign”
    • Butterfly shaped haematoma in perineum = urethral injury
63
Q

How would you investigate and manage penile fracture?

A

Investigations

  • Pre-op bloods and routine bloods as this will typically be diagnosed clinically and needs urgent repair

Management

  • Analgesia and anti-emetics
  • Urgent surgical exploration and repair
  • Abstinence from sexual activities for 6-8 weeks post op