Vanishing bile duct syndrome
Vanishing Bile Duct Syndrome (VBDS) is a rare but serious condition characterized by the progressive loss of bile ducts within the liver. This condition can lead to cholestasis, a condition where bile cannot flow from the liver to the duodenum.
Etiology[edit | edit source]
The exact cause of VBDS is unknown, but it is often associated with various diseases and conditions. These include autoimmune diseases, lymphoma, HIV, and adverse reactions to certain medications. In some cases, VBDS may occur after a liver transplant.
Symptoms[edit | edit source]
Symptoms of VBDS can vary, but often include jaundice, itching, and fatigue. As the disease progresses, patients may develop severe complications such as cirrhosis and liver failure.
Diagnosis[edit | edit source]
Diagnosis of VBDS is challenging due to its rarity and nonspecific symptoms. It is often diagnosed through a combination of liver function tests, imaging studies, and liver biopsy.
Treatment[edit | edit source]
Treatment of VBDS is primarily focused on managing symptoms and complications. This may include medications to reduce itching and ursodeoxycholic acid to improve bile flow. In severe cases, a liver transplant may be necessary.
Prognosis[edit | edit source]
The prognosis of VBDS varies widely and depends on the underlying cause and the patient's overall health. Early detection and treatment can improve the prognosis.
See also[edit | edit source]
References[edit | edit source]
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Contributors: Prab R. Tumpati, MD