Search Frames
Search No frames
PathWeb Home
©
Feed Back
About
Multicystic Renal Dysplasia
Click on Image to Enlarge it
Multicystic Renal Dysplasia

This is the left kidney of an 11 month old child which was clinically demonstrated to be non-functional. It was surgically removed and measured 5 cm in maximal diameter.
Note the multiple cysts.
The right kidney was non-cystic and appeared normal by imaging studies.
(Description By:H. Yamase, M.D. )
(Image Contrib. by: )
Cystic Renal Dysplasia
Etiology

This is a developmental disorder in metanephric differentiation.
It occurs sporadically and is not genetic.
Many cases have an associated lower tract obstructive lesion such as uretero-pelvic junction stenosis or occlusion, urethral valve or urethral atresia.
Pathogenesis

This is a developmental disorder in metanephric differentiation.
Many cases have an associated lower tract obstructive lesion such as uretero-pelvic junction stenosis or occlusion, urethral valve or urethral atresia.
There is a belief that the obstructive lesion is primary which then affects the normal differentiation of the renal parenchyma.,
Epidemiology

Cystic renal dysplasia is the most common form of cystic disease seen in the neonate.
General Gross Description

The cystic maldevelopment may be segmental and involve only portion of a kidney, or it may involve the whole kidney or both kidneys.
Although not conspicuous because of the cysts, the solid intervening parenchyma is also part of the maldevelopment.
The associated collecting structures (calyx, pelvis, ureter, bladder and urethra) may be atretic or obstructed.
General Microscopic Description

The histology of kidney shows multiple cysts of varying sizes lined by flat to cuboidal to columnar epithelium.
The stroma around cysts may show concentric collars of mesenchymal cells.
Islands of cartilage can sometimes be seen.
Clinical Correlation

Clinical manifestation of the disease will be dependent on the extent of renal parenchymal involvement and the obstructive lesions of the lower urinary tract if present.
Limited segmental disease may go undetected and be asymptomatic.
Bilateral diffuse involvement of the renal parenchyma would be fatal in the newborn.
References

Cotran RS, Kumar V, Robbins SL: Robbins Pathologic Basis of Disease. 5th ed. Philadelphia, W.B. Saunders, 1994, pp. 934-935.
Fetal and Neonatal Pathology, Keeling JW ed. New York: Springer-Verlag, 1987, pp. 412-414.
Cystic Renal Dysplasia
Synopsis by: Harold Yamase M.D. (T71000M23080)[417]
Search Medline at National Library of Medicine
Please be patient during transfer. Medline will open in a new window. To return, close the Medline Window
Search Frames
Search No frames
PathWeb Home
©
Feed Back
About