Difference between revisions of "Acquired cystic disease of the kidney"

From Libre Pathology
Jump to navigation Jump to search
(redirect)
Line 1: Line 1:
#redirect [[Cystic kidney diseases#Acquired renal cystic disease]]
'''Acquired renal cystic disease''', also '''acquired cystic disease''', is a benign change of the [[kidney]] seen in chronic renal failure.


==General==
*Thought to arise due to uremia,<ref name=pmid7861721>{{cite journal |author=Fick GM, Gabow PA |title=Hereditary and acquired cystic disease of the kidney |journal=Kidney Int. |volume=46 |issue=4 |pages=951–64 |year=1994 |month=October |pmid=7861721 |doi= |url=http://www.nature.com/ki/journal/v46/n4/pdf/ki1994354a.pdf}}</ref> not specific to the type of renal dialysis, i.e. hemodialysis vs. peritoneal dialysis.
*Presence of cysts dependent on duration of dialysis:<ref name=pmid7861721/>
**< 3 years ~44%.
**>4 years ~80%.
**>10 years ~90%.
*Associated with [[papillary renal cell carcinoma]].<ref>{{Ref DARP|438}}</ref>
==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 - location: cortex and medulla.
**Lined by simple flattened epithelium.
DDx:
*[[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]].
*[[Acquired cystic disease-associated renal cell carcinoma]].
==See also==
*[[Cystic kidney diseases]].
==References==
{{Reflist|1}}
[[Category:Genitourinary pathology]]
[[Category:Diagnosis]]
[[Category:Diagnosis]]

Revision as of 03:49, 27 April 2016

Acquired renal cystic disease, also acquired cystic disease, is a benign change of the kidney seen in chronic renal failure.

General

  • Thought to arise due to uremia,[1] not specific to the type of renal dialysis, i.e. hemodialysis vs. peritoneal dialysis.
  • Presence of cysts dependent on duration of dialysis:[1]
    • < 3 years ~44%.
    • >4 years ~80%.
    • >10 years ~90%.
  • Associated with papillary renal cell carcinoma.[2]

Microscopic

Features:[3]

  • Cysts - location: cortex and medulla.
    • Lined by simple flattened epithelium.

DDx:

See also

References

  1. ↑ 1.0 1.1 Fick GM, Gabow PA (October 1994). "Hereditary and acquired cystic disease of the kidney". Kidney Int. 46 (4): 951–64. PMID 7861721. http://www.nature.com/ki/journal/v46/n4/pdf/ki1994354a.pdf.
  2. ↑ Fogo, Agnes B.; Kashgarian, Michael (2005). Diagnostic Atlas of Renal Pathology: A Companion to Brenner and Rector's The Kidney 7E (1st ed.). Saunders. pp. 438. ISBN 978-1416028710.
  3. ↑ 3.0 3.1 Kessler M, Testevuide P, Aymard B, Huu TC (1991). "Acquired renal cystic disease mimicking adult polycystic kidney disease in a patient undergoing long-term hemodialysis". Am. J. Nephrol. 11 (6): 513–7. PMID 1819219.
Retrieved from "https://librepathology.org/w/index.php?title=Acquired_cystic_disease_of_the_kidney&oldid=43943"