Multicystic dysplastic kidney

Multicystic Dysplastic Kidney (MCDK) is a condition that occurs in the kidney where multiple cysts develop in place of healthy kidney tissue. It is usually diagnosed in infants and children and is a common cause of an abdominal mass in infants.

Causes[edit | edit source]

MCDK is a type of renal cystic disease that occurs when the kidneys do not develop normally while the baby is in the womb. The exact cause of MCDK is unknown, but it is thought to be related to problems with the ureteric bud, which is responsible for the development of the kidneys and the urinary tract.

Symptoms[edit | edit source]

The most common symptom of MCDK is a noticeable mass in the baby's abdomen. Other symptoms may include pain, blood in the urine, and high blood pressure. However, many children with MCDK do not have any symptoms.

Diagnosis[edit | edit source]

MCDK is usually diagnosed through ultrasound imaging during pregnancy or after birth. Other diagnostic tests may include a CT scan, MRI, or a nuclear medicine scan.

Treatment[edit | edit source]

There is no cure for MCDK, but the condition can be managed with regular monitoring and treatment of symptoms. In some cases, surgery may be required to remove the affected kidney.

Prognosis[edit | edit source]

The prognosis for children with MCDK is generally good. Most children do not experience any long-term health problems as a result of the condition. However, they may be at a higher risk of developing kidney disease later in life.

See also[edit | edit source]

Multicystic dysplastic kidney Resources
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