Horseshoe kidney pathophysiology: Difference between revisions

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==Overview==
==Overview==
Most people with horseshoe kidneys are totally asymptomatic and their kidneys function normally throughout their lives. About quarter of cases are found incidentally, usually during a CT scan due to some other problem. Nonetheless, there are lots of other patients who are predisposed to certain medical sequelae due to the embrogenesis or intrinsic anatomical abnormalities.
Most people with horseshoe kidneys are totally asymptomatic and their kidneys function normally throughout their lives. About quarter of cases are found incidentally, usually during a CT scan due to some other problem. Nonetheless, there are lots of other patients who are predisposed to certain medical sequel due to the embrogenesis or intrinsic anatomical abnormalities.
==Pathophysiology==
==Pathophysiology==
*Most people with horseshoe kidneys are totally asymptomatic and their kidneys function normally throughout their lives. About quarter of cases are found incidentally, usually during a CT scan due to some other problem. Nonetheless, there are lots of other patients who are predisposed to medical sequelae due to the embrogenesis or intrinsic anatomical abnormalities. These issues include:
Most people with horseshoe kidneys are totally asymptomatic and their kidneys function normally throughout their lives. About quarter of cases are found incidentally, usually during a CT scan due to some other problem. Nonetheless, there are lots of other patients who are predisposed to medical sequelae due to the embrogenesis or intrinsic anatomical abnormalities. These issues include:<ref name="pmid24178305">{{cite journal| author=Natsis K, Piagkou M, Skotsimara A, Protogerou V, Tsitouridis I, Skandalakis P| title=Horseshoe kidney: a review of anatomy and pathology. | journal=Surg Radiol Anat | year= 2014 | volume= 36 | issue= 6 | pages= 517-26 | pmid=24178305 | doi=10.1007/s00276-013-1229-7 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24178305  }}</ref>
*# Ureteropelvic junction obstruction : It is the most common problem in horseshoe kidney. It is caused by crossing of ureter over the fused isthmus leading to its obstruction.
* [[Ureteropelvic junction obstruction]] : It is the most common problem in horseshoe kidney. It is caused by crossing of ureter over the fused isthmus leading to its obstruction.
*# Kidney Stones : Stones usually occur when there is obstruction leading to decreased urine output and stasis of urine which create environment for stone formation.
* [[Nephrolithiasis]] : Stones usually occur when there is obstruction leading to decreased urine output and stasis of urine which create environment for stone formation.
*# Recurrent infections : Again due to stasis of urine, because stasis of urine create medium for bacterial growth
* Recurrent infections : Again due to stasis of urine, because stasis of urine create medium for bacterial growth.
*# Hydronephrosis : Basically it is caused by back-flow of urine due to obstruction of ureteropelvic junction.
* [[Hydronephrosis]] : Basically it is caused by back-flow of urine due to obstruction of [[Ureteropelvic junction obstruction|ureteropelvic junction]].
*# Increased incidence of certain cancers such as renal cell carcinoma, wilms tumor and carcinoid tumors.
* Increased incidence of certain cancers such as [[renal cell carcinoma]], [[Wilm's tumor]] and [[Carcinoid tumors]].<ref name="pmid12149688">{{cite journal| author=Neville H, Ritchey ML, Shamberger RC, Haase G, Perlman S, Yoshioka T| title=The occurrence of Wilms tumor in horseshoe kidneys: a report from the National Wilms Tumor Study Group (NWTSG). | journal=J Pediatr Surg | year= 2002 | volume= 37 | issue= 8 | pages= 1134-7 | pmid=12149688 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12149688  }}</ref>
 
==Genetics==
==Genetics==
[Disease name] is transmitted in [mode of genetic transmission] pattern.
*No genetic determination of horseshoe kidney is known, although it has been seen in identical twins and in siblings within the same family.<ref name="NatsisPiagkou2013">{{cite journal|last1=Natsis|first1=Konstantinos|last2=Piagkou|first2=Maria|last3=Skotsimara|first3=Antonia|last4=Protogerou|first4=Vassilis|last5=Tsitouridis|first5=Ioannis|last6=Skandalakis|first6=Panagiotis|title=Horseshoe kidney: a review of anatomy and pathology|journal=Surgical and Radiologic Anatomy|volume=36|issue=6|year=2013|pages=517–526|issn=0930-1038|doi=10.1007/s00276-013-1229-7}}</ref>
 
OR
 
Genes involved in the pathogenesis of [disease name] include:
*[Gene1]
*[Gene2]
*[Gene3]
 
OR
 
The development of [disease name] is the result of multiple genetic mutations such as:
 
*[Mutation 1]
*[Mutation 2]
*[Mutation 3]


==Associated Conditions==
==Associated Conditions==
Horseshoe kidney has been seen associated with other genetic disorders such as [[Turner syndrome]],[[Edwards syndrome]] and [[Down syndrome|Down's syndrome]].<ref name="pmid28613757">{{cite journal |vauthors=Kirkpatrick JJ, Leslie SW |title= |journal= |volume= |issue= |pages= |date= |pmid=28613757 |doi= |url=}}</ref><ref name="KletaBrämswig2000">{{cite journal|last1=Kleta|first1=Robert|last2=Brämswig|first2=Jürgen H.|title=Horseshoe kidney and Turner syndrome|journal=Nephrology Dialysis Transplantation|volume=15|issue=7|year=2000|pages=1094–1094|issn=1460-2385|doi=10.1093/ndt/15.7.1094-b}}</ref>


==Gross Pathology==
==Gross Pathology==
On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
Grossly, horseshoe kidney is usually fused at the lower of the kidney that is continuous along the mid line anterior to the great vessels. However complete fusion of the kidney produces a mass in the pelvis giving rise to two or more [[Ureter|ureters]].
 
[[File:Renalslide 32.png|center|thumb|courtesy of wikimedia]]
==Microscopic Pathology==
==Microscopic Pathology==
On microscopic histopathological analysis, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
On microscopic histopathology analysis, horseshoe kidney is normal unless there is secondary infection or [[obstructive nephropathy]].


==References==
==References==

Latest revision as of 20:16, 23 January 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:

Overview

Most people with horseshoe kidneys are totally asymptomatic and their kidneys function normally throughout their lives. About quarter of cases are found incidentally, usually during a CT scan due to some other problem. Nonetheless, there are lots of other patients who are predisposed to certain medical sequel due to the embrogenesis or intrinsic anatomical abnormalities.

Pathophysiology

Most people with horseshoe kidneys are totally asymptomatic and their kidneys function normally throughout their lives. About quarter of cases are found incidentally, usually during a CT scan due to some other problem. Nonetheless, there are lots of other patients who are predisposed to medical sequelae due to the embrogenesis or intrinsic anatomical abnormalities. These issues include:[1]

Genetics

  • No genetic determination of horseshoe kidney is known, although it has been seen in identical twins and in siblings within the same family.[3]

Associated Conditions

Horseshoe kidney has been seen associated with other genetic disorders such as Turner syndrome,Edwards syndrome and Down's syndrome.[4][5]

Gross Pathology

Grossly, horseshoe kidney is usually fused at the lower of the kidney that is continuous along the mid line anterior to the great vessels. However complete fusion of the kidney produces a mass in the pelvis giving rise to two or more ureters.

courtesy of wikimedia

Microscopic Pathology

On microscopic histopathology analysis, horseshoe kidney is normal unless there is secondary infection or obstructive nephropathy.

References

  1. Natsis K, Piagkou M, Skotsimara A, Protogerou V, Tsitouridis I, Skandalakis P (2014). "Horseshoe kidney: a review of anatomy and pathology". Surg Radiol Anat. 36 (6): 517–26. doi:10.1007/s00276-013-1229-7. PMID 24178305.
  2. Neville H, Ritchey ML, Shamberger RC, Haase G, Perlman S, Yoshioka T (2002). "The occurrence of Wilms tumor in horseshoe kidneys: a report from the National Wilms Tumor Study Group (NWTSG)". J Pediatr Surg. 37 (8): 1134–7. PMID 12149688.
  3. Natsis, Konstantinos; Piagkou, Maria; Skotsimara, Antonia; Protogerou, Vassilis; Tsitouridis, Ioannis; Skandalakis, Panagiotis (2013). "Horseshoe kidney: a review of anatomy and pathology". Surgical and Radiologic Anatomy. 36 (6): 517–526. doi:10.1007/s00276-013-1229-7. ISSN 0930-1038.
  4. Kirkpatrick JJ, Leslie SW. PMID 28613757. Missing or empty |title= (help)
  5. Kleta, Robert; Brämswig, Jürgen H. (2000). "Horseshoe kidney and Turner syndrome". Nephrology Dialysis Transplantation. 15 (7): 1094–1094. doi:10.1093/ndt/15.7.1094-b. ISSN 1460-2385.

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