Difference between revisions of "Autosomal recessive polycystic kidney disease"

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#redirect [[Cystic_kidney_diseases#Autosomal_recessive_polycystic_kidney_disease]]
'''Autosomal recessive polycystic kidney disease''', abbreviated '''ARPKD''', is an uncommon recessive genetic condition leading to [[renal failure]].
 
==General==
*Uncommon.
*Homogenous for mutated ''PKHD1 gene'' (polycystic kidney and hepatic disease).<ref name=omim263200>{{OMIM|263200}}</ref>
**The same gene is implicated in [[Caroli disease]].
*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.
 
DDx:
*[[Multicystic renal dysplasia]] - has larger variability of cyst size.
 
Images:
*[http://radiographics.rsna.org/content/20/3/837/F18.expansion ARPKD (radiographics.rsna.org)].<ref name=pmid10835131>{{Cite journal  | last1 = Lonergan | first1 = GJ. | last2 = Rice | first2 = RR. | last3 = Suarez | first3 = ES. | title = Autosomal recessive polycystic kidney disease: radiologic-pathologic correlation. | journal = Radiographics | volume = 20 | issue = 3 | pages = 837-55 | month =  | year =  | doi =  | PMID = 10835131 }}</ref>
*[http://radiology.uchc.edu/eAtlas/GU/529.htm ARPKD (radiology.uchc.edu)].
 
==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==
*[[Cystic kidney diseases]].
 
==References==
{{Reflist|1}}


[[Category:Diagnosis]]
[[Category:Diagnosis]]
[[Category:Cystic kidney diseases]]
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