Horseshoe kidney pathophysiology: Difference between revisions

Jump to navigation Jump to search
No edit summary
No edit summary
 
(16 intermediate revisions by 3 users not shown)
Line 1: Line 1:
<div style="-webkit-user-select: none;">
{| class="infobox" style="position: fixed; top: 65%; right: 10px; margin: 0 0 0 0; border: 0; float: right;"
{|class="infobox" style="position: fixed; top: 65%; right: 10px; margin: 0 0 0 0; border: 0; float: right;
|-
|-
| {{#ev:youtube|https://https://www.youtube.com/watch?v=mdKt8kLGfVA|350}}
| {{#ev:youtube|https://https://www.youtube.com/watch?v=mdKt8kLGfVA|350}}
Line 7: Line 6:
__NOTOC__
__NOTOC__
{{Horseshoe kidney}}
{{Horseshoe kidney}}
{{CMG}}
 
{{CMG}}; {{AE}}  
==Overview==
==Overview==
==Pathogenesis==
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.
The central portion of the kidney ends up inferior to the [[inferior mesenteric artery]], since its embryological ascent is arrested by its presence. This is the most common type of fusion anomaly in the kidneys.
==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:<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.
* [[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.
* [[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]], [[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==
*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>
 
==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==
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==
On microscopic histopathology analysis, horseshoe kidney is normal unless there is secondary infection or [[obstructive nephropathy]].
 
==References==
==References==
{{reflist|2}}
{{Reflist|2}}
 
{{WH}}
{{WH}}
{{WS}}
{{WS}}
[[Category:Needs content]]
[[Category: (name of the system)]]
[[Category:Disease]]
]
[[Category:Congenital disorders]]
[[Category:Kidney diseases]]

Latest revision as of 20:16, 23 January 2019

https://https://www.youtube.com/watch?v=mdKt8kLGfVA%7C350}}

Horseshoe kidney Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Horseshoe kidney from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-Ray

CT

MRI

Echocardiography and Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Horseshoe kidney pathophysiology On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Horseshoe kidney pathophysiology

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Horseshoe kidney pathophysiology

CDC on Horseshoe kidney pathophysiology

Horseshoe kidney pathophysiology in the news

Blogs on Horseshoe kidney pathophysiology

Directions to Hospitals Treating Horseshoe kidney

Risk calculators and risk factors for Horseshoe kidney pathophysiology

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.

Template:WH Template:WS ]