Primary Biliary Cholangitis – Lancaster

Primary Biliary Cholangitis - Lancaster

Primary Biliary Cholangitis - Lancaster

Primary biliary cholangitis (PBC), previously known as primary biliary cirrhosis, is an autoimmune disease that affects the liver. Here are the key points:

Bile Duct Damage:

  • PBC causes inflammation and gradual destruction of the small bile ducts in the liver.
  • Bile ducts play a crucial role in digestion, vitamin absorption, and cholesterol elimination.
  • Ongoing inflammation can lead to bile duct damage and permanent scarring (cirrhosis).

Symptoms:

  • Early symptoms (often asymptomatic):
    • Fatigue.
    • Itchy skin.
  • Later symptoms:
    • Yellowing of skin and eyes (jaundice).
    • Dry eyes and mouth.
    • Pain in the upper right abdomen.
    • Swollen spleen (splenomegaly).
    • Bone, muscle, or joint pain.
    • Swollen feet and ankles.
    • Ascites (fluid buildup in the abdomen).
    • Xanthomas (fatty deposits around eyes, eyelids, or joints).
    • Hyperpigmentation (darkening of skin).
    • Osteoporosis (brittle bones).
    • High cholesterol.
    • Steatorrhea (diarrhea with greasy stools).
    • Hypothyroidism.
    • Weight loss.

Causes:

  • Autoimmune Disease:
    • The immune system mistakenly attacks healthy bile duct cells.
    • Genetic and environmental factors likely contribute.
  • Liver Inflammation:
    • White blood cells (T cells) accumulate in the liver, damaging bile ducts.
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