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THE URINARY SYSTEM H.A MWAKYOMA, MD.

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Presentation on theme: "THE URINARY SYSTEM H.A MWAKYOMA, MD."— Presentation transcript:

1 THE URINARY SYSTEM H.A MWAKYOMA, MD

2 Urinary System Kidneys Ureters Bladder Urethra
Be sure to go over diagrams and other structures within the urinary system.

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5 URINARY BLADDER

6 Anatomy-Kidney

7 Components of Glomerulus:
Capillary basement membrane Mesangium Bowman capsule Cells Endothelial Epithelial Mesangial

8 Anatomy of Kidney

9 Anatomic Compartments
Glomerulus Tubules Blood vessels Interstitium Collecting system (Callices & Pelvis)

10 Kidney Functions: Excretion metabolic waste/drugs. Water/fluid balance. Electrolyte balance. Acid-base balance. Blood pressure. Erythropoietin secretion.

11 Anatomy of Kidney Glomerulus Loop of Henley PCT, DCT, CT
Note the positions of Glomerulus Loop of Henley PCT, DCT, CT Cortex, Medulla, Pelvis.

12 JGA GFR  Renin Angiotensin Blood Pressure

13 Filtration Membrane:

14 Normal Kidney:

15 Pathology definitions
Oliguria – a decrease in the amount of urine that is being passed. Polyuria – too much urine is being excreted Anuria – total suppression of urine formation and secretion Retention – the bladder does not release urine Hematuria – blood in the urine Uremia – toxic wastes in the blood Cystitis – inflammation of bladder Pyelitis – inflammation of the renal pelvis. Dysuria – painful urination

16 Kidney Diseases Developmental disorders Glomerular diseases
Tubulo-interstitial diseases Urinary stones Obstructive uropathy Tumors

17 Developmental disorders

18 Congenital Anomalies:
Agenesis – Potter syndrome Ectopia Fusion Dysplasia Simple cysts Polycystic kidney disease

19 Renal agenesis (Solitary kidney)
The total failure of a kidney to develop. Results from a failure of the embryonic renal bud or renal vascular system to form. Usually only occurs unilaterally

20 Bilateral renal agenesis

21 Unilateral renal ageneasis

22 Renal agenesis

23 Supernumerary kidney A third kidney that is usually small and rudimentary and possesses a separate pelvis, ureter, and blood supply

24 Partially fused supernumerary kidney with bifid ureter

25 Hypoplaisa (Hypoplastic kidney)
A kidney that is less developed than normal. It is often called a miniature kidney

26 Hypoplastic kidney with renal dysplasia

27 Renal Ectopia A misplaced kidney that are usually found in the pelvis and associated with a short ureter. The short ureter is the key factor to rule out Nephroptosis. pg143

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29 Anomalies of rotation, position and fusion
Mal-rotation One or both kidneys may produce a bizarre appearance of the renal parenchyma, calyces, and pelvis that suggest a pathological condition when in reality the kidney is normal

30 Anomalies of rotation, position and fusion
Nephroptosis The kidney falls down into the pelvis when a person stands up due to the pull of gravity Also called “floating kidney” or ectopic kidney

31 Crossed Ectopy One kidney lies either partially or completely across the midline and is fused with the other kidney at the lower pole.

32 Horseshoe kidney Both kidneys are joined at their lower poles across the midline of the body. Stones are more frequent The most common fusion anomalies

33 Horse Shoe Kidney

34 Horseshoe Kidney Situated usually in front of fouth lumbar vertebra
Fused lower poles common Ureters angulated Infection Nephrolithiasis Fixed mass below umbilicus

35 Complete Fusion Both of the kidneys are fused together in a single irregular mass which has no resemblance to a renal structure.

36 Polycystic kidney disease
Autosomal dominant (adult) (1:1,000) Autosomal recessive (infantile (1:30,000) Medullary cystic disease complex (1:10,000) Medullary sponge kidney Acquired cystic renal disease

37 Autosomal Dominant PKD
Common kidney disease (1:1,000) ADPKD-1 gene (polycystin) mutation 85% Bilaterally enlarged kidneys (>3,000g) Symptoms appear in adult life Renal failure 5-10 years thereafter

38 ADPKD:

39 ADPKD:

40 ADPKD Associated Conditions
Liver cysts (30%) Splenic cysts (10%) Pancreatic cysts (5%) Cerebral aneurysms (20%) Diverticulosis coli

41 Congenital cystic kidneys – polycystic kidneys
Hereditary Autosomal dominant trait Not usually detectable until the second or third decades of life and never manifests before the age of 30 Irregular upper quadrant mass Loin pain Haematuria Infection Hypertension Uraemia CT image : multiple cysts in both kidneys

42 URETERS Duplication of a ureter
The ureters usually join before they reach the bladder Less commonly the ureters open indepedently into the bladder Congenital megaureter

43 Double Ureter:

44 Ureteroceles Cyst like dilations of a ureter near its opening into the bladder. Radiographically it has the classic “cobra head” appearance. Like a diverticula only it goes into the bladder not out from it. When the bladder is full, it decrease the size of the ureterocele due to an increase in the pressure in the bladder. May cause obstruction if large enough.

45 URINARY BLADDER

46 Congenital defects of the bladder
Ectopia vesicae – exstrophy of the bladder Easily recognised at birth Umbilicus absent, protruding due to the intraabdominal pressure In addition epispadias Mons and clitoris bifid In the neonate the bladder should be covered with Saran Wrap or clingfilm to prevent trauma to the delicate mucosa

47 Ectopia vesicae – exstrophy of the bladder

48 Exstrophy of the bladder

49 A case of ectopia vesica with absent pelvic bone and herniated caecum

50 Diverticula The bladder or ureters are common areas for diverticula (out pouching of the wall). Best seen on a retrograde ureogram Because urine can stay in these areas for a long period of time, infections or irritations may occur.

51 bladder. Bladder Diverticulum

52 Congenital abnormalities of the urethra and penis
Meatal stenosis Congenital stricture Congenital valves Hypospadias epispadias

53 Meatus Congenital stenosis of the external urethral meatus – normally the narrowest part of the male urethra Associated with phimosis – at times pin hole meatus Back pressure effects Spraying, dribbling

54 Congenital Urethral Stricture
Rare

55 Congenital valves of the posterior urethra
Folds of urothelium Obstuction in boys Within prostatic urethra Catheter will pass easily Micturating cystourethrogram Pass catheter

56 Epispadias and Hypospadias
Hypospadias: congenital defect in which the urinary meatus is located on the lower or underside of the shaft Epispadias: congenital defect in which the urinary meatus is located on the upper side of the penile shaft; less common than hypospadias

57 Epispadias and Hypospadias
Clinical manifestations Ventral or dorsal placement of the urethral opening Altered urinary stream Chordee Diagnostic evaluation Based on physical examination

58 Hypospadias Most common urethral abnormality Glandular hypospadias
Coronal hypospadias Penile and penoscrotal hypospadias Perineal hypospadias Avoid circumcision

59 Normal External Urethral Meatus

60 Hypospadias types

61 Hypospadias

62 Phimosis At birth foreskin adherent to the surface of the glans penis
Separate spontaneously with time Can wait for 4 years to separate Gentle retraction at bath permitted Forcible retractions injure

63 Phimosis

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65 “To be a great champion you must believe you are the best
“To be a great champion you must believe you are the best. If you’re not, pretend you are.” – Muhammad Ali


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