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Ureterocele: Wikis

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Ureterocele
Classification and external resources
ICD-10 N28.8
ICD-9 593.89, 753.23
DiseasesDB 33455
eMedicine radio/729
MeSH D014518

A ureterocele is a congenital abnormality found in the urinary bladder. In this condition called ureteroceles, the distal ureter balloons at its opening into the bladder, forming a sac-like pouch. It is most often associated with a double collector system, where two ureters drain their respective kidney instead of one. Simple ureteroceles, where the condition involves only a single ureter, represents only twenty percent of cases. Ureteroceles strikes only one in 4,000 individuals, at least four fifths of whom are female. Patients are frequently Caucasian.

Since the advent of the ultrasound, most ureteroceles are diagnosed prenatally. The pediatric and adult conditions are often found only through diagnostic imaging performed for reasons other than suspicious ureteroceles.

Contents

Classification

Intravesical
Confined within the bladder
Ectopic
Some part extends to the bladder neck or urethra
Stenotic
Intravesical ureterocele with a narrow opening
Sphincteric
Ectopic ureterocele with an orifice distal to the bladder neck
Sphincterostenotic
Orifice is both stenostic and distal to the bladder neck
Cecoureterocele
Ectopic ureterocele that extends into the urethra, but the orifice is in the bladder

Signs and symptoms

The signs and symptoms of ureteroceles in the latter two forms can easily be confused with other medical conditions. Symptoms can include:

Complications

Many other complications arise from ureteroceles. Redundant collection systems are usually smaller in diameter than single, and predispose the patient to impassable kidney stones. The effective "bladder within a bladder" compounds this problem by increasing the collision of uric acid particles, the process by which uric acid stones are formed. Ureteroceles is also associated with poor kidney function. It can cause frequent blockage of the ureter leading to serious kidney damage. In other cases, a small, upper portion of the kidney is congenitally non-functional. Though often benign, this problem can necessitate the removal of non-functioning parts.

Causes

Definitive causes of ureteroceles have not been found. While the abnormal growth occurs within the uterus, it has not been substantiated that genetics are to blame.

Treatment · Single-system ureterocele Initial management is usually endoscopic incision of the ureterocele, which can be followed by surgical ureteric re-implantation to preserve renal function and prevent reflux. · Duplex-system ureterocele Treatment options vary with the individual and include: endoscopic incision; upper pole nephrectomy for a poorly functioning unit with ureterectomy or, where there is useful renal function, ureteropyelostomy can be performed.

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