Sympomatic Multicystic Dysplastic
Kidney
Multicystic
dysplastic kidney (MCDK) is a condition in which a child
is born with cysts covering the kidney – usually just one
kidney, but occasionally both. The cysts resemble bunches
of grapes. The cysts formerly were discovered when the infant
was born and examined. Today, with the common use of ultrasounds
during pregnancy, most of these are discovered at the 20-week
ultrasound.
The kidney eventually
shrinks in size and becomes deformed. Treatment of choice
is to leave it alone, as over time, it will be absorbed by
the body. (A normal life expectancy is typical for people
with just one kidney.) However, sometimes the kidney enlarges
in size and presses on the stomach or lungs, or the child
has abdominal pain, frequent urinary tract infections, incontinence
or other symptoms. The diagnosis then changes from MCDK to
symptomatic MCDK, and it may be advisable to remove the kidney.
Washington University physicians are the medical staff of Barnes-Jewish Hospital and St. Louis Children's Hospital
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