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Cystic_renal_dysplasia
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Cystic_renal_dysplasia

The photograph shows the amputated upper pole of a kidney removed for segmental cystic dysplasia.
The upper pole of this kidney had its own ureter which is seen here as a dilated and tortuous structure.
The equatorial and lower pole of the kidney was drained by a second ureter that was normal in caliber and continuous to the bladder.
(Description By:H. Yamase, M.D. )
(Image Contrib. by: UCHC )
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 belief that the obstructive lesion is primary and 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 a 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 manifestations of the disease will be dependent on the extent of renal parenchymal involvement and the obstructing 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. (T71000M23070)[473]
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