Download MBBS Surgery Presentations 15 Congenital Anomalies of Urinary Bladder Lecture Notes

Download MBBS (Bachelor of Medicine, Bachelor of Surgery) 1st Year, 2nd Year, 3rd Year and Final year Surgery 15 Congenital Anomalies of Urinary Bladder PPT-Powerpoint Presentations and lecture notes


























Urinary Bladder:

Congenital Anomalies

trauma, cystitis, tumors, urethral trauma

Anatomy

The urinary bladder is a hol ow, muscular, and distensible (or elastic)

organ that sits on the pelvic floor .

It is the organ that col ects urine excreted by the kidneys prior to

disposal by urination. Urine enters the bladder via the ureters and exits

via the urethra.

In males, the base of the bladder lies between the rectum and the

pubic symphysis. It is superior to the prostate, and separated from the

rectum by the rectovesical pouch.

In females, the bladder sits inferior to the uterus and anterior to the

vagina. It is separated from the uterus by the vesicouterine pouch.
















Anatomy.................

Embryology

The urogenital sinus is formed by the division of the cloaca

by the uro-rectal septum

The uro-genital sinus may be divided into three component

parts.



cranial portion which is continuous with the al antois and forms

the bladder proper.

The pelvic part of the sinus forms the prostatic urethra and

epithelium as wel as the membranous urethra and bulbo

urethral glands in the male and the membranous urethra and

part of the vagina in females.

the caudal portion forms the penile urethra in males and the

vestibule in females.




















Embryology........



The bladder forms from the cranial end of the urogenital sinus.

However, the trigone portion is formed by the caudal ends of the

mesonephric ducts. As the bladder expands, the mesonephric ducts

begin to become incorporated into the wal of the bladder dragging the

ureters along with them. Further growth causes the ureters to

eventual y have their own opening into the bladder.

The bladder is initial y continuous with the al antois. Over time, the

al antois degenerates to form a cord-like structure, the urachus. The

urachus goes from the umbilicus to the apex of the bladder and forms

the median umbilical ligament which can be seen in adults. The medial

umbilical ligaments may also be seen in adults on both sides of the

median umbilical ligament, these are the vestigial remnants of the

umbilical arteries.

Congenital Anomalies

A major consideration with congenital abnormalities is that they tend to

be multiple.


Al of these anomalies are infrequent or rare, and each condition occurs

in both males and females


Diagnosed in infancy or childhood

Most are discovered in the evaluation of a urinary tract infection or, in

the case of urachal anomalies, periumbilical drainage or redness.




























Classification

Urinary bladder anomalies are-

? bladder diverticula

? bladder ears

? congenital hypoplasia of the bladder

? megacystis

? bladder agenesis

? duplication anomalies of the bladder

? bladder septa

Urachal anomalies are

urachal sinus

urachal cyst

urachal diverticulum

patent urachus



Pathophysiology

The embryologic cause is unknown.

Bladder development occurs during the fifth to seventh

week of gestational development.

- Development depends upon many factors

- mesenchymal differentiation

- mesenchymal growth

- urine production

Bladder cycling, the process of sequential expansion and

contraction, is important in the anatomic and physiologic

development of the normal bladder.




















Bladder Diverticulum

Bladder diverticula are herniations of the bladder mucosa through

bladder wal musculature (detrusor muscle).

? Diverticular size can vary

? Diverticula can be wide or narrow mouthed.(The size of

diverticular openings has functional implications because narrow-

mouthed diverticula often empty poorly).

? Stasis of urine within diverticula can also lead to stone formation

or epithelial dysplasia.

? may cause ureteral obstruction,bladder outlet obstruction or

vesicoureteral reflux

Bladder Diverticulum...............



MC Site lateral and superior to the ureteral orifices. [dome of the

bladder, in disorders as bladder outlet obstruction (ie, posterior

urethral valves) or Eagle Barrett syndrome (prune bel y

syndrome)].

Congenital or acquired. Congenital deficiency or weakness in the

Waldeyer fascial sheath has been implicated as a cause.



Solitary
located at the junction of the bladder trigone and detrusor

Congenital diverticula are usual y removed surgical y












Bladder Diverticula

Bladder ears

lateral protrusions of the bladder through the internal inguinal ring and

into the inguinal canal.

Bladder ears are often observed during voiding cystourethrography

(VCUG) or intravenous pyelography (IVP), when the bladder is fil ed

to capacity.

Bladder ears have also been seen on CT body imaging.

No treatment is necessary


Knowledge of this entity is important to surgeons during inguinal

herniorrhaphy because occasional reports have been made of

partial or near total cystectomy performed under the mistaken

notion that this was a large hernia sac.






















Bladder agenesis

?

Rare

?

generally incompatible with life.

?

Ureters may enter into the urethra, vagina, Gartner duct cyst

(female), prostatic urethra, rectum, or the patent urachus.

?

Associated hydroureteronephrosis and renal dysplasia

(variable) are present.

?

Other associated anomalies include neurologic, orthopedic,

hindgut, and other urogenital anomalies, such as renal

agenesis and absence of the prostate, vagina, seminal

vesicles, epididymis, or penis

This condition requires urinary diversion and subsequent

reconstruction

Megacystitis

Megacystitis is an enlarged bladder, believed to be secondary to

overfil ing of the fetal bladder during development

Common presentations-

hydronephrosis.

Febrile urinary tract infection

high-grade vesicoureteral reflux

Megacystitis can be observed in other conditions, such as posterior

urethral valves, Ehlers-Danlos syndrome, urethral diverticulum,

microcolon hypoperistalsis syndrome, sacral meningomyelocele,

sacrococcygeal teratoma, and pelvic neuroblastoma.

Clean intermittent catheterization












Bladder duplication

v Rare

v Complete (2 urethras exist)

v Partial (the bladder joins distal y into one common

urethra)

v The 2 halves of the bladder are on either side of the midline,

with the corresponding ipsilateral ureter draining each bladder

half.

v Associated anomalies include duplication of the penis, vagina,

uterus, lumbar vertebrae, and hindgut. fistulas may be present

between the rectum, vagina, and urethra.

Duplication of Ur. bladder






















Urachal cyst

is a fluid-fil ed structure occurring in between the two obliterated

ends of the urachus.

Most occur in the distal third of the urachus.

More commonly, the urachal cyst is detected in early childhood or

adolescence.

Symptoms -infection ,inflammation,suprapubic mass, fever, pain,

and bladder or irritative voiding symptoms.

? (Staphylococcus aureus is the most common bacterial organism).

? Death from intra-abdominal rupture has been reported.

Patent urachus

Communication from the umbilicus to the bladder. continuous or

intermittent drainage from the umbilicus.



The tract may become inflamed, resulting in tenderness, periumbilical

swel ing, and serosanguinous or purulent discharge.

May be associated with bladder outlet obstruction, such as posterior

urethral valves.


Correction of the obstruction may result in the spontaneous resolution

of the patent urachus.




Patent Urachus

Patent Urachus




Resected specimen of Urachus

Intra-operative photograph






















Urachal sinus

derived from a persistently patent urachus

Children may present with

periumbilical tenderness

wet umbilicus

granulation tissue at the level of the umbilicus



In many instances, these children have undergone multiple sliver nitrate

cauterizations under the mistaken notion that this is simply
granulation tissue after severance of the remnant umbilical cord.


These can be observed in the first 4-8 weeks of life.

Ectopia Vesicae

open to the outside and turned inside-out, so that its inside is visible at birth,

protruding from the lower abdomen

Symptoms-

q Exposed posterior bladder wall

q Short lower abdominal wall

q Inguinal hernia

q Separated pubic rami

q Epispadias

q Incomplete fusion of genital tubercles
















q Opening in abdominal wall


q Urine excretion through opening in abdominal wall

q Incontinence

q Dilated ureters

q Open pubic arch

q Wide-set ischial bones

q Constriction between ureter and bladder


q Ureteral reflux

Exostrophy of Urinary bladder


Cystitis
















Cystitis

In women is common due to a number of reasons :

- short urethra

- pregnancy

- decreased estrogen production during menopause.
In men: mainly due to persistent bacterial infection of

the prostate.

In both sexes: common risk factors are :

- presence of bladder stone

- urethral stricture

- catheterization of the urinary tract

- diabetes mellitus

Pathogenesis of cystitis

Due to frequent irritation of the mucosal surfaces of

the urethra and the bladder.

Infection results when bacteria ascends to the urinary

bladder . These bacteria are residents or transient

members of the pereneal flora, and are derived from

the large intestine flora.



Toxins produced by uropathogens.
Condition that create access to bladder are:

- Sexual intercourse due to short urethral distance.
































Pathogenesis of cystitis

Uncomplicated UTI usually occurred in non

pregnant , young sexually active female without

any structural or neurological abnormality

Risk factors :

- Catheterization of the urinary bladder ,

instrumentation

- structural abnormalities

- obstruction
Hematogenous through blood stream ( less

common) from other sites of infection

Etiologic agents

E.coli is the most common (90%) cause of cystitis.

Other Enterobacteria include ( Klebsiella pnumoniae, Proteus spp.) Other gram negative rods

eg. P.aeroginosa.

Gram positive bacteria :Enterococcus fecalis, group B Strept. and Staphylococcus

saprophyticus { honeymoon cystitis}.

Candida species

Venereal diseases ( gonorrhea, Chlamydia) may present with cystitis.

Schistosoma hematobium in endemic areas.


































Pathogens involved

Uncomplicated UTI

Complicated UTI

E. coli

64%

Enterobacteriaceae 16%

E. coli

Enterococcus spp 20%

Enterobacteriaceae

% is

Pseudomona spp <1%

not

Pseudomonas spp

S. aureus

<1%

possibl

Acinetobacter spp

e to

Special cases

(judge often multiresistant

strains)

(S. epidermidis)

S. saprophyticus



Yeasts (catheter related result)

Viruses (Adeno, Varicel a)

Chlamydia trachomatis

Clinical presentation

Symptoms usually of acute onset

? Dysuria ( painful urination)
? Frequency ( frequent voiding)
? Urgency ( an imperative call for toilet)
? Haematuria ( blood in urine) in 50% of cases.
? Usually no fever.










Vaginitis (5%)

Candida spp.

T. vaginalis

Cystitis (80%)

Urethritis (10-

E. coli,

Dysuria and

15%)

S. saprophyticus

frequency

C. trachomatis,

Proteus spp.

N. gonorrhoeae

Klebsiella spp.

H. simplex

Other bacteria?

Non-infectious (<1%)

Hypoestrogenism

Functional obstruction

Mechanical obstruction

Chemicals

How to differentiate between cystitis and

urethritis ?

? Cystitis is of more acute onset

? More sever symptoms

? Pain, tenderness on the supra-pubic area.

? Presence of bacteria in urine ( bacteriuria)

? Urine cloudy, malodorous and may be

bloody


















Differential diagnosis

( types of cystitis)

Non-infectious cystitis such as:
1. Traumatic cystitis in women
2. Interstitial cystitis ( unknown cause, may be

due to autoimmune attack of the bladder)

3. Eosinophilic cystitis due to S.hematobium
4. Hemorrahagic cystitis due to radiotherapy or

chemotherapy.

Laboratory diagnosis of cystitis

1. Specimen col ection

2. Microscopic examination

3. Chemical screening tests












Recurrent cystitis

3 or more episodes of cystitis /year



Requires further investigations such as
Intravenous Urogram ( IVU) or ultrasound to detect
obstruction or congenital deformity

Cystoscopy required in some cases


















Treatment of cystitis

? Empiric treatment commonly used depending on

the knowledge of common organism and

sensitivity pattern

? Treatment best guided by susceptibility pattern

of the causative bacteria

? Common agents: Ampicil in, Cephradine,

Ciprofloxacin, Norfloxacin, Gentamicin or TRM-

SMX.

? Duration of treatment: 3 days for uncomplicated

cystitis

? 10-14 days for complicated and recurrent cystitis

? Prophylaxis required for recurrent cases by

Nitrofurantoin or TRM-SMX

? Prevention : drinking plenty of water and

prophylactic antibiotic










Bladder cancer

Aetiology

? Smoking ? 4x increased risk

? Causes 50% of cases

? Occupational ? rubber/dye industry

? Napthylamine, benzidine

? Schistosomiasis, chronic infection

? Medications ? cyclofosfamid, fenacetin




















Histology

? 90-95%

transitional-cell carcinoma

? 3%

squamos-cell carcinoma

? 2%

adenocarcinoma

? <1%

smal -cell carcinoma

? 99%

primary tumors

Entities

? 75-85% superficial bladder cancer

pTa, pTis, pT1

? 10-15% muscle-invasive bladder cancer

pT2, pT3, pT4

? 5%

metastatic bladder cancer

N+, M+














Presentation

? Classically painless frank haematuria,

sometimes intermittent

? Frequent urination, urgency

? symptoms with involvement of neighbouring

organs,lymphoedema, pelvic pain

Examination

History

Physical examination

Urine examination / urinalysis, cultivation,

cytology ? can be only 60% sensitive/

Ultrasound












Examination

? Cystoscopy is mandatory

? Biopsy or TURBT
? Bimanual pelvic examination /before and after

TURBT

? Chest X-ray
? IVU ? no routinely, (5% chance upper tract

involvement)

Bladder cancer: Stage and Prognosis




















Carcinoma in situ (CIS)

? Precursor infiltrating tumors
? Primary or secondary

? Subjectively ? frequent urination, urgency,

cystalgia

? Objectively ? no pathologies
? Laboratory

? Microhematuria
? Cytology positive (PAP IV-V)

CIS treatment

? Primary CIS: BCG

? Secondary CIS: TURB + BCG

? Recurrent CIS /after therapy/: cystectomy














Treatment

? Superficial Bladder Cancer

pTa, pT1, Tis

? Invasive bladder cancer
pT2-pT4


Superficial Bladder Cancer

pTa, pT1, Tis

Standard of care=intravesical therapy



transurethral resection bladder

tumors /TURBT/

Relapse rate: 70%



adjuvant therapy




TURBT

TURBT










TURBT

Superficial Bladder Cancer

Adjuvant Therapy

? Reduces relapse rate by 30-80%

? Mitomycin C ? in patient with

intermediate-risk BT

? BCG ? in patient with CIS, high risk BT






Invasive bladder cancer

? Standard of care = Radical cystectomy with

pelvic lymphadenectomy

? Only about 50% of patients with high-grade

invasive disease are cured

Radical cystectomy
















Radical cystectomy

Chemotherapy for bladder cancer

? Bladder cancer is a chemosensitive disease
? Active single agents RR



? Cisplatin

30%

? Carboplatin

20%

? Gemcitabine

20-30%

? Ifosfamide

20%


















Neoadjuvant chemotherapy

? Meta-analysis of ten randomised trials (2688 patients)

? 13% reduction in risk of death
? 5% absolute benefit at 5 years
? OS increased from 45% to 50%

? ABC Meta-analysis Collaboration. Lancet

2003;361:1927

Bladder-sparing therapy for invasive

bladder cancer

? High probability of subsequent distant metastasis after

cystectomy or radiotherapy alone (50% within 2 years)

? Radiotherapy in comparison with cystectomy has inferior

results (local control 40%)

? muscle-invasive bladder cancer is often a systemic

disease combined modality therapy








Bladder-sparing protocol

Transurethral resection

Induction Therapy: Radiation + chemotherapy
(cisplatin, paclitaxel)

Cystoscopy after 1 month

no tumor

tumor

Consolidation: RT + CT

cystectomy

Urinary diversion

? Diversion of urinary pathway from its natural path

? Types:

? Temporary
? Permanent




A nephrostomy is a

surgical procedure by

which a tube, stent, or

catheter is inserted

through the skin

into the kidney

Cutaneous

Ureterostomy...

One kidney drainage,

with short-live

prognosis

Complications

(infection, stone,

stenosis)








Permanent urinary diversion

? Uretero ? sigmoidostomy

? Ileal conduit

? Colon conduit

? Ileocaecaecal segment

Cutaneous urinary

diversions

Ileal conduit (ileal loop)

A 12 cm loop of ileum led out

through abdominal wall

Stents used

The space at cystectomy site

drained by a drainage system

After surgery a skin barrier

and a transparent disposable

urinary drainage bag

Constantly drains
















Complications of ileal conduit

? Wound infection

? Wound dehiscence

? Urinary leakage

? Ureteral obstruction

? Small bowel obstruction

? Ileus

? Stomal gangrene

? Narrowing of the stoma

? Pyelonephritis

? Renal calculi












Continent Urinary Diversions

? Continent Ileal Urinary Reservoir
Indiana Pouch
? Most common continent urinary diversion
? Periodically catheterized
Koch Pouch
Ureterosigmoidostomy
? Voiding occurs from rectum

Uretero-

sigmoideostomy










Uretero- sigmoidostomy

? Complications:

? Reflux of urine

? Hyperchloraemic acidosis (ammonium chloride

reabsorption, bicarbonates secretion)

? Renal infection

? Stricture formation










Potential complications

? Peritonitis due to disruption of anastomosis

? Stoma ischaemia and necrosis due to

compromised blood supply to stoma

? Stoma retraction and separation of

mucocutaneous border due to tension or

trauma


Bladder Reconstruction












INJURIES OF THE URINARY BLADDER

? Bladder injuries occur most often from external force and are often associated

with pelvic fractures.

? Iatrogenic injury may result from gynecologic and other extensive pelvic

procedures as well as from hernia repairs and transurethral operations.

Classification

? closed and open

? isolated and combined

? intraperitoneal,

retroperitoneal and mixed.




















Clinical Findings

? There is usually a history of lower abdominal trauma.

? Blunt injury is the usual cause

? Patients ordinarily are unable to urinate, but when

spontaneous voiding occurs, gross hematuria is usually

present

? Most patients complain of pelvic or lower abdominal pain.

Clinical Findings

? Heavy bleeding associated with pelvic fracture

may result in hemorrhagic shock, usual y from
venous disruption of pelvic vessels.

? An acute abdomen indicates intraperitoneal

bladder rupture.

? A palpable mass in the lower abdomen usual y

represents a large pelvic hematoma.

? On rectal examination, landmarks may be

indistinct because of a large pelvic hematoma.






















Clinical Findings

? Laboratory Findings:

? Catheterization usually is required in patients

with pelvic trauma but not if bloody urethral

discharge is noted.

? When catheterization is done, gross or, less

commonly, microscopic hematuria is usually

present.

? Urine taken from the bladder at the initial

catheterization should be cultured to determine

whether infection is present.

X-Ray Findings

? A plain abdominal film generally

demonstrates pelvic fractures.

There may be haziness over the

lower abdomen from blood and

urine extravasation.

? An intravenous urogram should

be obtained to establish whether

kidney and ureteral injuries are

present.


















X-Ray Findings

? Bladder disruption is shown on cystography.

? Retrogradual cystography help to differentiate

penetrating and unpenetrating, intraperitoneal

and retroperitoneal ruptures of the bladder,

locate urinary flow and approximate site of

rupture.

? The sign of retroperitoneal rupture is

accumulation of X-ray contrast matter in

perivesical fat tissue.

? With intraperitoneal extravasation, free

contrast medium is visualized in the

abdomen, highlighting bowel loops.

X-Ray Findings






















Treatment

? A. Emergency Measures:

Shock and hemorrhage should be treated.

? B. Surgical Measures

Treatment

In a case of retroperitoneal complete rupture

of the bladder it is exposed by suprapubic

extraperitoneal access carefully inspected

and is juncture by two-row catgut junctures.

Drainage by means of epicystostomy is

necessary.

Operation finish with drainage of perivesical

and pelvic tissue.

In order to prevent formation of urinary flow,

in all cases of retroperitoneal rupture of

urinary bladder, perivesical space is

drainage through obturatorial foramen or

ischiorectal space.




























Treatment

Intraperitoneal bladder ruptures should be

repaired via a transperitoneal approach after

careful transvesical inspection and closure of

any other perforations.

The peritoneum must be closed carefully

over the area of injury.

The bladder is then closed in separate

layers by absorbable suture.

All extravasated fluid from the peritoneal

cavity should be removed before closure.

At the time of closure, care should be taken

that the suprapubic cystostomy is in the

extraperitoneal position.

Urethral Injuries

? Urethral injuries are uncommon and

occur most often in men, usual y

associated with pelvic fractures or

straddle-type fal s.

? Various parts of the urethra may be

lacerated, transected, or contused.

? Management varies according to the

level of injury.

? The urethra can be separated into 2

broad anatomic divisions: the posterior

urethra, consisting of the prostatic and

membranous portions, and the anterior

urethra, consisting of the bulbous and

pendulous portions
























Clinical Findings

Symptoms:
? lower abdominal pain and inability to urinate. A history of crushing

injury to the pelvis is usual y obtained.

Signs:
? Blood at the urethral meatus is the single most important sign of

urethral injury (Urethroragia).

? Suprapubic tenderness and the presence of pelvic fracture are noted

on physical examination.

? A large developing pelvic hematoma may be palpated.

? Perineal or suprapubic contusions are often noted.

? Rectal examination may reveal a large pelvic hematoma with the

prostate displaced superiorly.

Clinical Findings

? Laboratory Findings:

? Anemia due to hemorrhage may be noted.

? Urine usually cannot be obtained initially, since the patient

should not void and catheterization should not be
attempted.
















X-Ray Findings

Fractures of the bony pelvis are

usually present.

A urethrogram (using 20-30 ml of

watersoluble contrast material)

shows the site of extravasation.

Ordinarily, there is free extravasation

of contrast material into the

perivesical space.

Incomplete prostatomembranous

disruption is seen as minor

extravasation, with a portion of

contrast material passing into the

prostatic urethra and bladder.

X-Ray Findings




























Treatment

? Conservative therapy is effective for

patients with recent nonpenetrating

damage of urethra: rest, cool

compresses, and antibiotics.

? Within 7-8 days after trauma thermal

procedures and resorption agents are

prescribed.

? In case of ischuria instead of a high

cystotomy it is possible to perform

troacar epicystostomy.

? Shock and hemorrhage should be

treated.

Treatment

Surgical Measures:

? Urethral catheterization should be avoided.

? suprapubic cystostomy to provide urinary

drainage.

? The bladder should be opened and

carefully inspected for lacerations. If a

laceration is present, the bladder should

be closed with absorbable suture material

and a cystostomy tube inserted for urinary

drainage.

? The suprapubic cystostomy is maintained

in place for about 3 months. This allows

resolution of the pelvic hematoma, and the

prostate and bladder will slowly return to

their anatomic positions.
























Film Suprapubic Cystostomy

Treatment

Urethral reconstruction ?

? Reconstruction of the urethra after prostatic

disruption can be undertaken within 3 months.

? Before reconstruction, a combined cystogram

and urethrogram should be done to determine

the exact length of the resulting urethral

stricture.

? The preferred approach is a single-stage

reconstruction of the urethral rupture defect

with direct excision of the strictured area and

anastomosis of the bulbous urethra directly to

the apex of the prostate.

?

? A 16F silicone urethral catheter should be left

in place along with a suprapubic cystostomy.

? Catheters are removed within a month, and

the patient is then able to void












Re-do end to end

Complications

? Stricture, impotence, and incontinence are complications of prostato

membranous disruption.

? Stricture fol owing primary repair and anastomosis occurs in about one-

half of cases. If the preferred suprapubic cystostomy approach with
delayed repair is used, the incidence of stricture can be reduced to
about 5%.

? The incidence of impotence after primary repair is 30-80% (mean, about

50%).

? Incontinence in primary reanastomosis is noted in one-third of patients.

? Delayed reconstruction reduces the incidence to less than 5%.

This post was last modified on 08 April 2022