Difference between revisions of "Medical kidney diseases"

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(→‎ADPKD: +more)
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*Childhood onset - autosomal recessive polycystic kidney disease (ARPKD).
*Childhood onset - autosomal recessive polycystic kidney disease (ARPKD).


==ADPKD==
==Autosomal dominant polycystic kidney disease (ADPKD)==
===Etiology===
===General===
====Etiology====
*Mutation in ''PKD1'' gene or ''PKD2'' gene.
*Mutation in ''PKD1'' gene or ''PKD2'' gene.
*Is classified in a large group of diseases - ''ciliopathies''.
*Is classified in a large group of diseases - ''ciliopathies''.
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*Assoc. with colonic diverticula, aortic aneurysm, mitral valve prolapse.
*Assoc. with colonic diverticula, aortic aneurysm, mitral valve prolapse.


===Liver and PKD===
====Liver and PKD====
Complications:<ref name=Ref_MacSween174-5>{{Ref MacSween|174-5}}</ref>
Complications:<ref name=Ref_MacSween174-5>{{Ref MacSween|174-5}}</ref>
#Infected cyst.
#Infected cyst.
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See also: ''[[Medical liver disease]]''.
See also: ''[[Medical liver disease]]''.
===Gross===
Features:
*Cysts.
DDx: acquired renal cystic disease.
==Acquired renal cystic disease==
===General===
*Due hemodialysis.
===Microscopic===
Features:<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>
*Cysts: cortex and medulla.


==Transplant - rejection==
==Transplant - rejection==