Chapter 14 Renal Pathology power point Flashcards
Angiomylolipoma- (hamartoma)
Cysts
Pathology – Benign
a mass composed of fat, blood vessels and smooth muscle tissue
Highly echogenic , homogenous.
Angiomylolipoma- (hamartoma)
simple,parapelvic,hemorrhagic,multicystic dysplastic,polycystic kidney disease, (autosomal recessive and autosomal dominant)
Cysts
Most common renal mass
Spherical, smooth wall, anechoic, posterior acoustic enhancement
Normally asymptomatic, unless they become large and compress adjacent renal tissue
Clinically insignificant
50% of the population > age 50 have these
Simple renal cyst
cyst projects outward away from the kidney
Exophytic
cyst lies within the renal cortex
Cortical
cyst that originates in the renal parenchyma and protrude into the renal sinus
Parapelvic
cyst that originate in the renal sinus
Peripelvic
A cyst that does not meet the diagnostic criteria of a simple cyst
Septations, internal debris, mural nodules, papillary projections, irregular borders are worrisome for malignancy and will be followed up with other imaging modalities or surgery
Renal cell carcinoma can manifest as a multicystic mass
Complex renal cysts
Autosomal Dominant Polycystic Kidney Disease (ADPKD) also known as Adult Polycystic Disease (APKD)
Normally lies dormant for many years and manifests itself in the third to fourth decade (30-40 years of age)
Patient may also develop multiple cysts of varying sizes in other organs including pancreas, liver and spleen
40% associated with polycystic liver disease
Polycystic kidney disease
Can be asymptomatic until third to fourth decade of life Decreased renal function UTI Renal calculi Flank pain Hematuria Palpable abdominal mass
clinical findings of APKD
Autosomal recessive (ARPKD)- relatively rare genetic disorder divided into four types depending on onset.
- Perinatal-found in-utero, common leading factor for demise. Oligohydramnios and enlarged echogenic kidneys
- Neonatal
- Infantile
- Juvenille
Polycystic kidney disease
Often recognized in the fetus
Confirmed with a postnatal ultrasound
Perinatal death often occurs
Secondary complications of renal failure and hepatic disease often causes early death
Bilateral disease, loss of corticomedullary differentiation
arpkd
Renal failure
Hepatic disease
Clinical findings of ARPKD
a mass composed of fat, blood vessels and smooth muscle tissue
Highly echogenic , homogenous
Usually discovered incidentally
Unilateral
Patients with tuberous sclerosis have a tendancy to develop these, usually bilateral
Not painful unless there is hemorrhage within the mass
Angiomylolipoma- (hamartoma)