Congenital portosystemic shunt

Congenital portosystemic shunt is a rare condition that is present at birth, in which blood vessels do not form properly in the liver. This condition can lead to serious health problems, such as liver damage and heart failure.

Overview[edit | edit source]

A congenital portosystemic shunt is a condition in which the blood vessels that normally carry blood from the intestines and spleen to the liver are either missing or malformed. This can cause blood to bypass the liver, leading to a buildup of toxins in the bloodstream.

Symptoms[edit | edit source]

Symptoms of congenital portosystemic shunt can vary widely, but may include:

Jaundice (yellowing of the skin and eyes)
Encephalopathy (brain disease, damage, or malfunction)
Hepatomegaly (enlarged liver)
Ascites (accumulation of fluid in the abdominal cavity)

Causes[edit | edit source]

The exact cause of congenital portosystemic shunt is unknown, but it is thought to occur during fetal development. It is not believed to be inherited.

Diagnosis[edit | edit source]

Diagnosis of congenital portosystemic shunt typically involves imaging tests, such as an ultrasound, CT scan, or MRI. A liver biopsy may also be performed.

Treatment[edit | edit source]

Treatment for congenital portosystemic shunt typically involves surgery to correct the abnormal blood vessels. In some cases, a liver transplant may be necessary.

Prognosis[edit | edit source]

The prognosis for individuals with congenital portosystemic shunt varies widely, depending on the severity of the condition and the individual's overall health.

See also[edit | edit source]

Congenital portosystemic shunt Resources
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