Pathology of the Kidneys and UUT Flashcards
(33 cards)
Cysts
Simple cysts
Complex cysts
Parapelvic cysts
Use Bosniak grading to determine risk of malignancy
Exact cause unknown More common as people age Asymptomatic; rarely cause problems Do not affect renal function If large enough, can cause dull pain in flank or back, fever, and upper abdo pain. Can be solitary or multiple Can involve one or both kidneys
Ultrasound presentation:
Anechoic, well defined, thin-walled, fluid-filled structure with posterior enhancement
Complex cysts
Considered malignant until proven benign
Ultrasound presentation:
May contain septations, thick walls, calcifications, internal echoes, and mural nodularity
Parapelvic cysts
Usually ovoid in shape
Originate from the renal sinus
Most likely lymphatic in origin
Do not communicate with the collecting system **
Largely asymptomatic, but may occasionally cause pain, haematuria, hypertension, or obstruction
Multicystic Dysplastic Kidney Disease (MCDK)
Abnormal development in utero Attributed to genetics Affects one kidney only Multiple cysts of varying sizes “Bunch of grapes” Non-functioning kidney
Polycystic Kidney Disease
Can be autosomal dominant (ADPKD) or autosomal recessive (ARPKD)
Both forms can lead to renal failure
ADPKD
Twenty times more common
Appears later in life (40+ years)
By age 60 years, approximately 50% of people with ADPKD have end-stage renal disease
Cysts arise from any nephron segment
Bilateral disease
Enlarged kidneys with multiple asymmetrical cysts
ARPKD
- Diagnosed in utero or shortly after birth
- Can present with symmetrically enlarged echogenic kidneys that retain their shape
- “Cysts” are dilatations of the collecting duct
- In older children, kidneys are enlarged with echogenic cortex and medulla, and corticomedullary differentiation is lacking
Benign solid tumours
Make up about 15-20% of all solid renal tumours in the parenchyma
Four types: Renal adenomas Angiomyolipomas Lipomas Leiomyomas
Renal adenoma
Most common benign renal tumours
Arises from mature tubular cells
Almost always less than 3cm in size
Can’t differentiate them from other solid renal tumours
Types include:
Renal oncocytoma
Papillary adenomas
Ultrasound presentation:
Echogenic or isoechoic well-circumscribed lesion <3cm, but some can be larger
Angiomyolipoma
Composed of fat, muscle, and blood vessels
Tumour size varies between 1 and 20 cm
May be multifocal
Incidental finding
Ultrasound presentation:
Well circumscribed echogenic solid lesion (mostly!)
Leiomyoma
Rare
Smooth muscle tumour
Renal Cell Carcinoma (RCC)
The most common of all renal neoplasms 85 - 95%
Twice as common in men >40yrs
Develops in the sixth or seventh decade of life
Clinical presentation:
Often non-specific
Haematuria, flank pain and palpable mass
Ultrasound presentation:
Most RCC’s are isoechoic, however can be hyperechoic
Transitional Cell Carcinoma (TCC)
Rare type of kidney cancer (more in week 8)
Most common bladder and lower UT cancer (ureter, urethra), can arise from the renal pelvis or calyx
Clinical presentation:
Pain in back
Haematuria
Frequent urination
Ultrasound presentation:
Solid hypoechoic lesion/s originating within the renal pelvis or calyx
Lymphoma
Renal lymphoma is usually seen as a part of spectrum of multi-systemic lymphoma, however, rarely may be seen as a primary disease
Ultrasound presentation:
Solid hypoechoic lesion/s
Wilm’s tumour
Nephroblastoma
Often affects children 3-4 years of age, less common after 5 years of age
The most common cancer in children
Clinical presentation:
Constipation
Abdo pain, swelling, or discomfort
N & V & fever, LOA
Ultrasound presentation:
Large solitary, predominantly solid and echogenic mass
May contain cystic areas – multiloculated mass
Can be present in utero
Renal metastases
The most common renal metastases arise from carcinomas, such as lung, colorectal, ENT, breast, soft tissue, and thyroid
Clinical presentation:
Flank pain
Haematuria
Weight loss
Ultrasound presentation :
Variable!
Hydronephrosis
Causes:
- Blockage of urine flow down ureter
Internal blockage i.e. calculi, scarring in the ureter, tumour blocking VUJ
External blockage i.e. mass effect compressing ureter closed
- Vesicoureteric reflux (pathology lecture in week 8)
Vesicoureteric reflux:
Failure of the bladder to empty properly
Most common in babies and young children
Can be unilateral or bilateral
Urine refluxes from bladder back up into kidney
Bacteria from bladder can reach the kidney
Can lead to kidney infection and kidney damage
Pyelonephritis
Urinary tract infection that starts in urethra or bladder and travels to the kidney/s
Main cause – gram negative bacteria (i.e. E. coli), most often from faeces
P/W fever, nausea, frequent urination, pain in back, side, or groin
Needs medical attention asap – antibiotics +/- hospitalisation
Ultrasound presentation:
Can involve one or both kidneys
Can involve partial or whole kidney/s (focal or diffuse)
Echogenic wedge-defect if partial pyelonephritis
Loss of blood flow seen on colour Doppler
Renal abscess
Complication of pyelonephritis
Two types: renal and perirenal
Both start with tubular necrosis
Renal abscesses form a walled-off cavity
Perirenal abscesses appear as a more diffuse liquification area between the renal capsule and fascia
Pyonephrosis
Pyo = pus
Pus, debris, or haemorrhage seen within a dilated pelvicalyceal system
Ultrasound presentation:
Echoes seen within the pelvicalyceal system
Can sometimes look solid
Glomerulonephritis
Inflammation of the glomeruli
Can be acute or chronic
Usually affects both kidneys
Early diagnosis and treatment needed to prevent renal failure
Causes:
Staphylococcal infection (strep throat)
Immunologic illnesses
Renal scarring
Caused by recurrent UTIs – reflux, pyelonephritis
Permanent damage to parenchyma
Reduction in function
Ultrasound presentation:
Appears “on top” of the medullae, not between them
Thinned parenchyma
Renal atrophy
- Kidneys are smaller than expected given a person’s age and height
- Can be congenital (renal hypoplasia) or acquired
- Congenital renal atrophy doesn’t treatment; check for normal thickness of parenchyma
- Acquired due to lower blood supply to the kidneys and / or loss of nephrons.
- Can be due to chronic infections or hydronephrosis
Renal failure
- End-stage kidney disease
- Kidneys no longer adequately filter the blood of waste products or control level of fluid in the body
- As kidney disease progresses, GFR decreases. By end-stage kidney disease, GFR is less than 15ml per minute
- Can be acute or chronic
- Treatment – dialysis or transplant
Ultrasound presentation:
Acute – may appear normal in size or be enlarged and hypoechoic with parenchymal disease
Chronic – small, echogenic kidneys with loss of normal anatomy