S9: embryology & obstructions Flashcards
Where do the three separate kidney systems form from?
Organisation of intermediate mesoderm
3 systems develop sequentially
Disappearance of one system marks the onset of development of the next developmental stage
1st appears in the cervical region – the pronephros
Describe the pronephros
First kidney system, never functions in humans
Important because of its duct – pronephric duct extends from the cervical region to the cloaca and drives the development of the next developmental stage
Describe the mesonephros
Mesonephric tubules develop caudal to the pronephric region
Mesonephric tubules plus mesonephric duct = embryonic kidney
-mesonephric duct has important role in the development of the repro system in the male
-sprouts the ureteric bud which induces development of the definitive kidney
No water conserving function -> need to upgrade
Describe the metanephros
Undifferentiated intermediate mesoderm, caudal to the mesonephros Ureteric bud induces development of the true kidney, metanephros in this tissue Ureteric bud (releases growth factors) contacts metanephric blastema -> bud expands and branches -> renal pelvis, minor & major calyces
Describe the development of the renal functional unit
Ureteric bud drives the development of the definitive kidney
Collecting system is derived from the ureteric bud itself
The excretory component is derived from intermediate mesoderm under the influence of the ureteric bud
Describe the ascent of the kidney
Metanephric kidney first appears in the pelvic region
Undergoes an apparent caudal to cranial shift, crossing the arterial fork formed by vessels returning blood from the fetus to the placenta
Swaps position with the gonads
What is a pelvic kidney?
Ascent of the kidney fails
What is a horseshoe kidney?
Poles of the kidney fuse together
Can be caught further down by mesenteric artery
What is an ectopic urethral orifice?
Splitting of the ureteric bud
Partial or complete
Symptomatic consequence is ectopic urethral opening
Describe the urogenital sinus
Created from hindgut by urorectal septum
UGS is continuous with umbilicus – urachus closes to become median umbilical ligament
Superior part connects to umbilicus
Majority differentiates to form the urinary bladder
Inferior part develops into the urethra – sex differences in structural development of the urethra
Describe development of the urethra in females
Mesonephric ducts (MD) reach urogenital sinus (UGS)
Ureteric bud sprouts from MD
UGS begins to expand & MD begins to regress
MD regression continues, ureteric bud opens into UGS
Describe development of the urethra in males
Mesonephric ducts (MD) reach urogenital sinus (UGS)
Ureteric bud (UB) sprouts from MD
Smooth musculature begins to appear, UGS begins to expand
UB & MD make independent openings in UGS
List causes of urinary retention
Calculi Pregnancy Benign prostatic hypertrophy Recent surgery Drugs Urethral strictures
Compare acute and chronic urinary retention
Acute – painful inability to void, residual volume 300-1500ml
Chronic – painless, may still be voiding, residual volume 300-4000ml
Describe management of acute urinary retention
Catheterise and record residual urinary volume
History, examination, urine dip, U&Es
Treat any obvious cause
BPH – alpha blocker, may trial without catheter after 1-2 weeks
Describe management of chronic urinary retention
Catheterise and record residual volume
History, examination, urine dip, U&Es
High pressure -> abnormal U&Es, hydronephrosis, repeat episodes can cause permanent renal scarring and CKD
Low pressure -> normal renal function, no hydronephrosis
Plan for long-term catherization or intermittent self-catherization
Describe post-obstructive diuresis
Following resolution of urinary retention through catherization
Kidneys can often over-diurese -> can lead to worsening AKI
Urine output should be monitored for 24 hours post catheterisation – patients with high urine volumes should be supported with IV fluids
Describe hydronephrosis
Dilation of the renal pelvis and calyces (build-up of urine) due to obstruction at any point in the urinary tract causing increased pressure and blockage:
1) Unilateral – upper urinary tract obstruction
2) Bilateral – lower urinary tract obstruction
Progressive atrophy of the kidney develops from the back pressure from the obstruction and is transmitted to the distal parts of the nephron
GFR declines and if obstruction is bilateral, the patient goes into renal failure
What is the difference between hydronephrosis and hydroureter?
Hydronephrosis = obstruction at the pelviureteric junction
Hydroureter = obstruction at the ureter (eventually developing hydronephrosis)
Bladder distension with hypertrophy = obstruction of the bladder neck/urethra (eventually leads to hydroureter and hydronephrosis)
Describe acute ureteric obstruction
Renal colic, caused by calculus but can also be blood clots or sloughed papilla
Usually, a unilateral problem
Leads to acute renal failure if bilateral – anuria/oliguria
Pyonephrosis can develop – infected, obstructed kidney & failure to promptly decompress may lead to death from sepsis and permanent loss of renal function
Describe diagnosis of an upper urinary tract obstruction
Diagnosis with CT or USS – show structure, not function
Diuretic renography is a functional test
List ways to drain the upper urinary tract
Nephrostomy
JJ stent
Describe urolithiasis
Risk factors: men, Caucasians
Dehydration increases the concentration of the urine & is a predisposing factor
Can form anywhere in the urinary tract – 3 most common sites: pelviureteric junction, pelvic brim & vesicoureteric junction
CT scan gold standard for diagnosing stones
Outline the 5 types of calculi
Calcium oxalate stones – associated with hypercalcaemia, primary hyperparathyroidism & hyperoxaluria
Mixed calcium phosphate and calcium oxalate stones – associated with alkaline urine
Magnesium ammonium phosphate stones – associated with urea splitting bacteria
Uric acid stones – associated with gout and myeloproliferative disorders
Cystine stones – patients with inherited cystinuria