Horseshoe kidney overview: Difference between revisions

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===Primary Prevention===
===Primary Prevention===
There are no established measures for the primary prevention of horseshoe kidney disease.


===Secondary Prevention===
===Secondary Prevention===
There are no established measures for the secondary prevention of horseshoe kidney disease.


==References==
==References==

Revision as of 03:54, 19 January 2019

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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

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

Overview

Horseshoe kidney is the congenital disorder of kidneys in which the isthmus of both kidneys fuse together during embryonic development leading to appearance of "Horseshoe". It is the most common fusion defect of kidneys.

Historical Perspective

Before 1800 A.D. horseshoe kidney regarded as curiosity found only at postmortem examination.However with the advent of the roentgen rays and the intravenous pyelography the diagnostic possibilities to recognize the horseshoe kidney improved, which was later on aided by the ultrasound and computed tomography scan by which horseshoe kidney can be easily diagnosed.

Classification

Horseshoe kidney may be classified into three groups based on:

  1. morphological appearance of fusion,
  2. Site of the fusion,
  3. Vascular supply or angiographic appearance of the vessels.

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 certain medical sequelae due to the embrogenesis or intrinsic anatomical abnormalities.

Causes

During early fetal development, the kidneys are developed in the pelvis and then later they move upwards in abdomen. Sometimes due to unknown reason the lower ends of both kidneys fuse together forming a 'U' shaped single kidney.

Differentiating Horseshoe kidney from Other Diseases

There are other forms of kidney fusion defects. Usually they can be differentiated based on appearances on CT scan.

Epidemiology and Demographics

  • It is fairly common condition with 1 case in every 500 live births.
  • Males cases are twice more common than female cases.
  • Although it has been seen in members of same families, but no any particular gene has been found to cause this disease.

Risk Factors and Associations

There are no particular gene discovered yet which are directly related to horseshoe kidney but it has been seen associated with other genetic disorders such as Turner syndrome and Edwards syndrome, further suggesting that it is linked to some genes.

Screening

There is no particular screening test for horseshoe kidney itself, although CT scanning or renal ultrasonography can be used to screen for the presence of stones, masses, or hydronephrosis.

Natural History, Complications, and Prognosis

  1. Hydronephrosis
  2. Renal stones
  3. Urinary tract infections
  4. Renal Cancer

Diagnosis

Diagnostic Study of Choice

Intravenous pyelography is considered the best initial test.

History and Symptoms

1 in every 3 patients remain asymptomatic throughout their lives. Other patients present with symptoms secondary to urinary tract infections, renal stones and obstruction. These symptoms include dysuria, flank pain and fever.

Physical Examination

Because the kidneys are lower in abdomen, a midline lower abdominal mass can be felt during physical examination.

Laboratory Findings

Urine routine (DR) and urine culture should be done to look for any sign of urinary infection and serum creatinine and electrolytes should be done to check the kidney function.

X-ray

X-ray may show renal outlines lower than in normal person, but other than that it is not that much useful.

Ultrasound

Renal Ultrasound can be used to look for presence of any stones, masses, obstruction or hydronephrosis.

CT scan

CT Scan with contrast is imaging technique of choice. CT Scan of abdomen and pelvis with and without contract is used to look for location of kidneys. It is accurate in determining the anatomical location and also help in differentiating the parenchymal from fibrous isthmus.

MRI

MRI is also helpful in diagnosing horseshoe kidney, and is used in conditions where CT Scan is not recommended or available. MRI is also costlier than CT Scan.

Other Imaging Findings

Other imaging studies such as Renal scintigraphy, also known as "renal scans", can also be used in the diagnosis of horseshoe kidney, by accessing its anatomical structure,renal function and drainage.

Treatment

Treatment for the horseshoe may not be required, if no symptoms.However, supportive treatment can be given depending upon the symptoms.

Medical Therapy

Pharmacologic medical therapy is recommended among patients with Urinary tract infection.

Interventions

Surgery

Although most of the people doesn't require surgical intervention but it depends upon the disease process itself and its complications.

Primary Prevention

There are no established measures for the primary prevention of horseshoe kidney disease.

Secondary Prevention

There are no established measures for the secondary prevention of horseshoe kidney disease.

References


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