9. Urinary bladder
Embryology
• Epithelium is of two types
• Endodermal – Cranial part of vesicourethral canal
• Mesodermal – Mesonephric duct
• Trigone is mesodermal in origin and the rest is
endodermal
12. • Female urethra formed by – Primitive urethra
- Some part of UGS
• Male Urethra
- Prostatic urethra - develop same as female
urethra
- Membranous urethra - From the Pelvic part of
urogenital sinus
- Penile urethra – Phallic part of UGS
17. DUPLEX RENAL PELVIS AND
URETER
• Congenital condition in which ureteric bud splits or
arises twice ,resulting in two ureters draining
single kidney.
18. DUPLEX RENAL PELVIS AND
URETER
• Most common (1 in 150 births)
• Unilateral duplication >Bilateral duplication (6:1)
• Common on left side
• Female > Male
22. Weigert meyer Law
• In complete type,upper ureter ends distally and
medially to normal ureteric orifice.
• Whereas, lower ureter end proximally and lateral to
normal ureteric orifice.
23.
24. Clinical features
• In adults - usually asymptomatic
• In children – presents with Vesicoureteric reflux
resulting in infection , stone
formation and hydronephrosis
25. Investigations
• IVU - diagnostic
• Cystoscopy- double ureteric orifice on the same
side
• DTPA scan – Function
26.
27. Treatment
• Ureteric meatotomy (if narrowing of orifice)
• Treatment of complications(UTI, hydronephrosis)
• Heminephrectomy +removal of corresponding
ureter
28. ECTOPIC URETER
• Ureter rather than terminating at the urinary
bladder, terminates at different site.
• Associated with duplicated renal collecting system.
• 10% bilateral
• Female> male (7:1)
29. In females
opens either into urethra or into the vagina
leading to incontinence.
In males
opens above the external urethral sphincter.
30. Other sites-
• apex of the trigone
• posterior urethra
• seminal vesicle or
• ejaculatory duct
• can be associated with renal dysplasia ,
frequent UTI, and urinary incontinence.
31.
32. Treatment
• Partial nephrectomy – severely diseased or atrophic
• Reimplantation – refluxing ureter
• In females- hydronephrotic and chronically infected
kidney – best to excise
33. URETEROCOELE
• Cystic enlargement of the intramural ureter
• probably due to atresia of the ureteric orifice
• Female>Male (4:1)
• 10% are bilateral.
34.
35. • Ureters with ureterocoele drains the upper
pole frequently
• Associated with dysplastic or non functional
renal tissue
36. Clinical features
• In children – present with infection
• If large - obstruct the bladder neck or contralateral
orifice
• In adults – typically presents with stones in lower
ureter
41. CONGENITAL MEGAURETER
• Uncommon condition
• Common in males
• Ureteric dilatation with or without obstruction
• May be bilateral and associated with other congenital
abnormalities
42. • . Cause – aperistalsis of distal ureter
dilatation
(cutoff value for megaureter >6 or 7mm)
• Most cases of megaureter with obstruction present in
childhood with severe infections.
• Renal stones can easily form in the dilated systems.
44. • Whitaker test
Saline or contrast injected through a percutaneous
needle or nephrostomy tube at a rate of 10ml/min.
Catheter in bladder to monitor intravesical pressure.
<15cm H2O - normal
>22cm H2O - obstruction
48. DIVERTICULA OF THE BLADDER
Two types :
1. Congenital diverticula are the result of a
developmental defect.
2. Acquired
49. CONGENITAL BLADDER
DIVERTICULA
• Represents unobliterated vesical end of
urachus.
• Situated midline anterosuperiorly.
• Mouth of diverticulum situated above and to the
outer side of one ureteric orifice.
• Rare type and common in boys.
50. ❖ Normal intravesical pressure during voiding =35–50
cmH2O
❖Hypertrophic bladder(due to obstruction) = 150
cmH2O may be reached
Saccule formation
Diverticulum
ACQUIRED BLADDER DIVERTICULA
51.
52. Symptoms
• Usually asymptomatic.
• Poor emptying of bladder
As diverticula do not contain
a defined functional muscularis propria
• Diagnosed incidentally.
53. • Investigations
Urine culture and sensitivity
Cystoscopy and cystogram
Intravenous urogram
Ultrasound abdomen
CT scan abdomen
56. Management
• Removal of diverticula through open surgery
• Suprapubic transverse extraperitoneal approach
• Combined intravesical and extravesical
diverticulectomy
57. BLADDER EXTROPHY
• Incomplete development of infraumbilical part of
anterior abdominal wall and anterior wall of
bladder.
• Common in males (4:1)
58. Clinical Features
• Penis – Broad and short
• Urine dribbling
• Undescended testis
• B/L inguinal hernia may be present
• Separation of pubic bone (Pubic diastesis)
• In females – Bifid Clitoris
59. Other features
• Often associated with spina bifida
• Protusion of red mucus membrane of posterior
bladder wall
• Umbilicus is absent
• In males, epispadias commonly present with
rudimentary prostate and seminal vesicle.
60.
61.
62. Management
• Bladder is closed in first year of life after osteotomy.
• Later reconstruction of bladder neck and sphincter
is required.
• But now one stage reconstruction is done
• Urinary diversion may also be done
65. POSTERIOR URETHRAL VALVE
• 1/5000-8000 Live male births
• Valve are Membranous with small slit in them.
• It lies just distal to verumontanum.
• Act as unidirectional valves- causing obstruction
to antegrade urinary flow but catheter can be
passed retrogradely.
66. Clinical Features
• UTI
• Uremia
• Renal failure
If valves are incomplete ,Child is asymptomatic and
diagnosed late.
67. Diagnosis
• Should be detected and treated as early as possible.
• Antenatal Ultrasound - B/L Hydronephrosis
- Distended bladder
• Voiding cystogram
- Dilatation of urethra above the valves
70. HYPOSPADIAS
• External meatus opens on the underside of the
penis any where proximal to the normal site.
• Most common congenital abnormality of urethra.
• 1/200-300 Male live births
72. Characteristic Features
1.Ventrally placed meatus
• Downward directed stream of
urine
• Sperm deposition incorrect →
Infertility
2.Ventral curvature of penis
(Chordee)
3.Dorsal hood of prepuce
73. Surgery
Indication
1. To improve sexual
function
2. To correct urinary
stream
3. Cosmetic reason
• Completed by 18
months
Orthoplasty
Substitution
urethroplasty
Meatoplasty
scrotoplasty
74. Surgery
• Chordee correction - Netbit Procedure
• Urethroplasty
• MAGPI - For coronal hypospadias
• Tubularized Incised Plate urethroplasty - For distal
Hypospadias
• Preputial flap repair - For proximal hypospadias
75. EPISPADIAS
• Very rare
• Urethral opening is on the dorsum of the penis
• A/w Upward Curvature of penis
• Coexist with Bladder Extrophy
78. Anterior Diverticulum
• Saccular outpouching arising from the ventral
surface of anterior urethra
Clinical presentation
• Straining at micturition
• Swelling of penis during micturition
• Followed by dribbling of urine and disappearance of
the swelling
79.
80.
81.
82. Management
• Minor cases - Endoscopic Incision of the flap of
the urethral mucosa between the two lumens
• Severe cases – excision of the diverticulum and
primary repair of the urethra
86. PHIMOSIS
• At birth foreskin is normally adherent to glans penis
• Adhesions disappear around 2 years but may persist
till 6 years
87. • PHIMOSIS in children -
scarring of prepuce causing
inability to retract
foreskin resulting in :
- Ballooning of the
foreskin during micturition
- Balanoposthitis
- Urinary obstruction
(sometimes)
88. • Phimosis in adults – Occurs as a result of
- Balanitis
- Posthitis
- Balanitis xerotica obliterans
96. CIRCUMCISION IN ADULTS
• Dorsal slit over skin upto corona and then
circumferentially and ventrally and later skin is cut
with inner layer.
• Frenular artery is transfixed and ligated ventrally.
• Skin is apposed to cut end of corona.
• Postoperatively, antibiotics and analgesics are
given.