Chronic liver disease and hepatomegaly Flashcards

1
Q

Chronic liver disease and hepatomegaly

A

This man complains of weight loss and abdominal discomfort. His GP has referred him to you for further opinion. Please examine his abdomen.

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2
Q

Signs of chronic liver disease

A
  • General: Cachexia, Icterus (also in acute), Excoriation and Bruising
  • Hands: Leuconychia, Clubbing, Dupuytren’s Contractures and Palmar Erythema
  • Face: Xanthelasma, Parotid Swelling and Fetor Hepaticus
  • Chest and Abdomen: Spider Naevi and Caput Medusa, Reduced body hair, Gynaecomastia and Testicular Atrophy (in males)
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3
Q

Signs of hepatomegaly

A

• Palpation and percussion:
⚬⚬ Mass in the right upper quadrant that moves with respiration, you can’t get above and is dull to percussion
⚬⚬ Estimate size (finger breadths below the diaphragm)
⚬⚬ Smooth or craggy/nodular (malignancy/cirrhosis)
⚬⚬ Pulsatile (TR in CCF)
• Auscultation
⚬⚬ Bruit over the liver (hepatocellular carcinoma)

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4
Q

Evidence of an underlying cause of hepatomegaly

A
  • Tattoos and needle marks: Infectious hepatitis
  • Slate‐grey pigmentation: Haemochromatosis
  • Cachexia: Malignancy
  • Mid‐line sternotomy scar: CCF
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5
Q

Evidence of treatment

A
  • Ascitic drain/tap sites

* Surgical scars

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6
Q

Evidence of decompensation

A
  • Ascites: shifting dullness
  • Asterixis: ‘liver flap’
  • Altered consciousness: encephalopathy
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7
Q

Causes of hepatomegaly

A

The big three:

  1. Cirrhosis (alcoholic)
  2. Carcinoma (secondaries)
  3. Congestive cardiac failure
  4. Plus:
    Infectious (HBV and HCV),
    Immune (PBC, PSC and AIH)
    Infiltrative (amyloid and myeloproliferative disorders)
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8
Q

Investigations

A
  • Bloods: FBC, clotting, U&E, LFT and glucose
  • Ultrasound scan of abdomen
  • Tap ascites (if present)
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9
Q

Investigations If cirrhotic

A
• Liver screen bloods:
⚬⚬ Autoantibodies and immunoglobulins (PBC, PSC and AIH)
⚬⚬ Hepatitis B and C serology
⚬⚬ Ferritin (haemochromatosis)
⚬⚬ Caeruloplasmin (Wilson’s disease)
⚬⚬ α‐1 antitrypsin
⚬⚬ AFP (hepatocellular carcinoma)
• Hepatic synthetic function: INR (acute) and albumin (chronic)
• Liver biopsy (diagnosis and staging)
• ERCP (diagnose/exclude PSC)
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10
Q

Investigations If malignancy

A
  • Imaging: CXR and CT abdomen/chest
  • Colonoscopy/gastroscopy
  • Biopsy
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11
Q

Complications of cirrhosis

A
  • Variceal haemorrhage due to portal hypertension
  • Hepatic encephalopathy
  • Spontaneous bacterial peritonitis
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12
Q

Child‐Pugh classification of cirrhosis

A
Prognostic score based on bilirubin/albumin/INR/ascites/encephalopathy
Class----Score----1 year survival
A:---------5–6----------100%
B:---------7–9-----------81%
C:---------10–15--------45%
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13
Q

Causes of Ascites

A
  • Cirrhosis (80%)
  • Carcinomatosis
  • CCF
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14
Q

Treatment of ascites in cirrhotics

A
  • Abstinence from alcohol
  • Salt restriction
  • Diuretics (aim: 1 kg weight loss/day)
  • Liver transplantation
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15
Q

Causes of palmar erythema

A
  • Cirrhosis
  • Hyperthyroidism
  • Rheumatoid arthritis
  • Pregnancy
  • Polycythaemia
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16
Q

Causes of gynaecomastia

A

1• Physiological: puberty and senility
2• Klinefelter’s syndrome
3• Cirrhosis
4• Drugs, e.g. spironolactone and digoxin
5• Testicular tumour/orchidectomy
6• Endocrinopathy, e.g. hyper/hypothyroidism and Addison’s

17
Q

Autoantibodies in liver disease

A
  • Primary biliary cirrhosis (PBC): antimitochondrial antibody (M2 subtype) in 98%, increased IgM
  • Primary sclerosing cholangitis (PSC): ANA, anti‐smooth muscle may be positive
  • Autoimmune hepatitis (AIH): anti‐smooth muscle, anti liver/kidney microsomal type 1 (LKM1) and occasionally ANA may be positive (pattern helps classify)