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Difference between revisions of "Cystic kidney diseases"
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*[[Autosomal dominant polycystic kidney disease]] rarely,<ref name=pmid1819219>{{cite journal |author=Kessler M, Testevuide P, Aymard B, Huu TC |title=Acquired renal cystic disease mimicking adult polycystic kidney disease in a patient undergoing long-term hemodialysis |journal=Am. J. Nephrol. |volume=11 |issue=6 |pages=513–7 |year=1991 |pmid=1819219 |doi= |url=}}</ref> see ''Microscopic'' in [[ADPKD]]. | *[[Autosomal dominant polycystic kidney disease]] rarely,<ref name=pmid1819219>{{cite journal |author=Kessler M, Testevuide P, Aymard B, Huu TC |title=Acquired renal cystic disease mimicking adult polycystic kidney disease in a patient undergoing long-term hemodialysis |journal=Am. J. Nephrol. |volume=11 |issue=6 |pages=513–7 |year=1991 |pmid=1819219 |doi= |url=}}</ref> see ''Microscopic'' in [[ADPKD]]. | ||
==Autosomal recessive polycystic kidney disease== | |||
*Abbreviated ''ARPKD''. | |||
===General=== | |||
*Uncommon. | |||
*Homogenous for mutated ''PKHD1 gene'' (polycystic kidney and hepatic disease).<ref name=omim263200>{{OMIM|263200}}</ref> | |||
*Associated with congenital hepatic fibrosis | |||
Subdivided into:<ref name=Ref_Klatt235>{{Ref Klatt|235}}</ref> | |||
*Neonatal. | |||
*Infantile. | |||
*Juvenile. | |||
===Gross=== | |||
Features:<ref name=Ref_Klatt235>{{Ref Klatt|235}}</ref> | |||
*Marked bilateral enlargement - may almost fill the abdomen. | |||
*Smooth cortical surface. | |||
*Poorly demarcated corticomedullary junction. | |||
===Microscopic=== | |||
Features:<ref name=Ref_Klatt236>{{Ref Klatt|236}}</ref> | |||
*Numerous cysts of the collecting ducts. | |||
**Typically radially arranged. | |||
**Lined by cuboidal cells. | |||
*Abnormally low number of glomeruli. | |||
=See also= | =See also= | ||