Choluria

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Choluria[edit | edit source]

Diagram illustrating the mechanism of choluria.

Choluria is a medical condition characterized by the presence of bile pigments in the urine, which gives it a dark brown or tea-like color. This condition is often associated with liver diseases, particularly those that involve the obstruction of bile flow, such as cholestasis, hepatitis, or cirrhosis.

Pathophysiology[edit | edit source]

Choluria occurs when there is an excess of bilirubin in the bloodstream, which is then excreted in the urine. Normally, bilirubin is processed by the liver and excreted into the bile, which then enters the gastrointestinal tract. However, in conditions where the liver is unable to process bilirubin effectively, or where there is an obstruction in the bile ducts, bilirubin levels in the blood increase, leading to its excretion in the urine.

Causes[edit | edit source]

Choluria can be caused by a variety of conditions, including:

Clinical Presentation[edit | edit source]

Patients with choluria may notice that their urine is darker than usual. This change in urine color is often accompanied by other symptoms of liver dysfunction, such as jaundice, pruritus, and fatigue.

Diagnosis[edit | edit source]

The diagnosis of choluria involves:

Treatment[edit | edit source]

Treatment of choluria focuses on addressing the underlying cause. This may involve:

  • Medications to treat liver inflammation or infection.
  • Surgical procedures to remove obstructions in the bile ducts.
  • Lifestyle changes to support liver health, such as avoiding alcohol and maintaining a healthy diet.

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Contributors: Prab R. Tumpati, MD