Cystic kidney diseases: Difference between revisions

From Libre Pathology
Jump to navigation Jump to search
← Older edit
Michael (talk | contribs)
49,299 edits
Michael (talk | contribs)
49,299 edits
No edit summary
 
(2 intermediate revisions by the same user not shown)
Line 24: Line 24:
==Autosomal dominant polycystic kidney disease==
==Autosomal dominant polycystic kidney disease==
*Abbreviated ''ADPKD''.
*Abbreviated ''ADPKD''.
===General===
{{Main|Autosomal dominant polycystic kidney disease}}
====Etiology====
*Mutation in ''PKD1'' gene or ''PKD2'' gene.
*Is classified in a large group of diseases - ''ciliopathies''.
 
PKD1 related disease:<ref name=Ref_MacSween174-5>{{Ref MacSween|174-5}}</ref>
*Encodes polycystin.
*Death at ~53 years.
*Assoc. with cerebral aneurysms.
 
PKD2 related disease:<ref name=Ref_MacSween174-5>{{Ref MacSween|174-5}}</ref>
*Death at ~69 years.
*Associated with colonic diverticula, [[aortic aneurysm]], [[mitral valve prolapse]].
 
====Liver cysts and PKD====
=====General=====
Features:
*Most common extra-renal manifestation of PKD; dependent on age, sex and renal function:<ref name=pmid9186898>{{cite journal |author=Perrone RD |title=Extrarenal manifestations of ADPKD |journal=Kidney Int. |volume=51 |issue=6 |pages=2022–36 |year=1997 |month=June |pmid=9186898 |doi= |url=http://www.nature.com/ki/journal/v51/n6/pdf/ki1997276a.pdf}}</ref>
**Age dependence:
***10-17% <40 years old have liver cysts.
***70-75% >60 years old have liver cysts.
**Renal function:
***60-70% of patients with [[end-stage renal disease]] (ESRD) and near-ESRD.
**Females more often affected.
*Hepatic function usu. preserved.
 
Complications:<ref name=Ref_MacSween174-5>{{Ref MacSween|174-5}}</ref>
#Infected cyst.
#[[Cholangiocarcinoma]].
 
=====Microscopic=====
Features:
*''Von Meyenburg complexes'':
**Cluster of dilated ducts with "altered" bile.
**Surrounded by collagenous stroma.
 
See: ''[[Medical liver disease]]''.
 
===Gross===
Features:
*Thin walled cysts.
**Number of cysts:
***If you can count 'em it favours acquired renal cystic disease... if you can't it favours the genetic condition.
 
===Microscopic===
Features:<ref name=Ref_DARP426>{{Ref DARP|426}}</ref>
*Cysts lined by simple flattened epithelium.
*Normal renal tubules interspersed between cysts.
*+/-Fibrosis (late-stage).
 
DDx:
*[[Acquired renal cystic 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>
**Morphologically similar to acquired renal cystic disease.<ref name=rj_oct2010>RJ. 20 October 2010.</ref>
**It is said that "... if you can count 'em it's simple cysts; if you can't it's polycystic (renal disease)."<ref name=rj_oct2010>RJ. 20 October 2010.</ref><ref>{{cite book |author= Barbaric, Zoran L.  |title=[http://books.google.com/books?id=uABgezxjhYwC&pg=PA87&lpg=PA87&dq=cystic+renal+disease,+%22if+you+can+count+them%22&source=bl&ots=GYyIdR9YmS&sig=DBYzT8LO2MltLA-wwW-0QwnQ6Lk&hl=en&ei=0hF-Taz0IsG3twe5yfG6BQ&sa=X&oi=book_result&ct=result&resnum=1&ved=0CBoQ6AEwAA#v=onepage&q=cystic%20renal%20disease%2C%20%22if%20you%20can%20count%20them%22&f=false Principles of Genitourinary Radiology] |publisher=Thieme |location= |year=1994 |pages= 87 |edition=2nd |isbn=978-0865774933 |oclc= |doi= |accessdate=}}</ref>
 
===Sign out===
<pre>
Left Kidney, Nephrectomy:
- Polycystic kidney with changes of chronic renal failure (thyroidization),
  consistent with polypcystic kidney disease.
- NEGATIVE for malignancy.
</pre>


==Acquired renal cystic disease==
==Acquired renal cystic disease==
{{Main|Acquired renal cystic disease}}
{{Main|Acquired cystic disease of the kidney}}


==Autosomal recessive polycystic kidney disease==
==Autosomal recessive polycystic kidney disease==
Line 104: Line 43:
*[[Kidney tumours]].
*[[Kidney tumours]].
*[[Bosniak classification]].
*[[Bosniak classification]].
*[[Multicystic dysplastic kidney]].


=References=
=References=

Latest revision as of 16:45, 4 February 2025

Polycystic kidneys. (WC/CDC)

Cystic kidney diseases, also cystic renal diseases, are a group of medical kidney diseases characterized by multiple cysts.

Renal neoplasms, e.g. renal cell carcinoma, may be cystic. They are dealt with in kidney tumours.

Overview

Adult

Pediatric

Specific diseases

Benign cortical cyst of the kidney

  • AKA benign cortical cyst.
Main article: Benign cortical cyst of the kidney

Autosomal dominant polycystic kidney disease

  • Abbreviated ADPKD.
Main article: Autosomal dominant polycystic kidney disease

Acquired renal cystic disease

Main article: Acquired cystic disease of the kidney

Autosomal recessive polycystic kidney disease

  • Abbreviated ARPKD.
Main article: Autosomal recessive polycystic kidney disease

Localized cystic disease of the kidney

  • AKA segmental cystic disease of the kidney.
  • AKA unilateral cystic disease of the kidney.
  • AKA benign multilocular cyst of the kidney.
Main article: Localized cystic disease of the kidney

See also

References

Retrieved from "https://librepathology.org/w/index.php?title=Cystic_kidney_diseases&oldid=53413"