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Hépatomégalie

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What is hepatomegaly?

Hepatomegaly is enlargement of the liver. The liver edge is normally palpable in children and thin adults and some patients may have a palpable right lobe of the liver. It is smooth, uniform, non-tender and descends to meet the palpating fingers on inspiration. The best way to assess liver size is by percussion - a normal-sized liver can appear enlarged if displaced downwards by lung disorders. An enlarged liver expands down and across towards the left iliac fossa (LIF). To avoid missing a really big liver, always begin liver palpation in the LIF and work towards the right upper quadrant1 .

The most common causes of hepatomegaly in the UK are alcoholic liver disease, malignancy (particularly metastases) and congestive cardiac failure.

Hepatomegaly symptoms

  • Associated hepatomegaly symptoms may be few or rather vague - eg, loss of appetite, weight loss and lethargy.

  • There may be hepatomegaly symptoms relating to liver dysfunction - eg, jaundice, bruising, gynaecomastia, spider naevi, ascites; or related to the underlying cause - eg, xanthelasma suggests autoimmune liver disease.

  • Measure the hepatomegaly by percussing the upper and lower borders (will rule out causes such as emphysema which can push the liver down giving a false impression of hepatomegaly).

On palpation

Smooth hepatomegaly
Suggests: hepatitis, chronic heart failure, sarcoid, early alcoholic cirrhosis, tricuspid incompetence with a pulsatile liver.

Craggy hepatomegaly
Suggests: primary hepatoma or secondary tumours.

NB: a small liver is typical in late cirrhosis and nodular cirrhosis typically produces a small shrunken liver not a large craggy one. Ask particularly about alcohol consumption, sexual activity, intravenous (IV) drug abuse, blood transfusions and recent travel.

Hepatomegaly causes (aetiology)1 2 3

Infection

Viral hepatitis (acute and chronic).

Infectious mononucleosis - Epstein-Barr virus (EBV).

Cytomegalovirus (CMV).

Paludisme.

Helminthic infection.

Pyogenic abscess.

Amoebic abscess.

Congestive

Insuffisance ventriculaire droite.

Congestive cardiac failure (CCF).

Péricardite constrictive.

Syndrome de Budd-Chiari.

Autoimmune

Autoimmune liver disease.

Biliary disease

Extrahepatic obstruction - eg, pancreatic cancer, cholangiocarcinoma.

Cirrhose biliaire primitive.

Primary sclerosing cholangitis.

Tumours and infiltrative diseases

Secondaries (metastatic carcinoma).

Primary hepatic tumour - eg, hepatocellular.

Lymphome.

Granulomatous hepatitis.

Amylodose.

Sarcoïdose.

Haematological disorders

Thalassaemia.

Sickle cell disease.

Haemolytic anaemia.

Myeloma.

Leucémie.

Métabolique

Hémochromatose.

Wilson's disease.

Glycogen storage diseases.

Porphyria.

Stéatose hépatique non alcoolique.

Diabetes mellitus-associated fatty liver.

Toxic/drug-related

Alcoholic liver disease: acute alcoholic hepatitis and alcoholic fatty liver.

Drug-induced hepatitis - eg, statins, macrolides, amiodarone, paracetamol (indicates significant damage).

Hepatomegaly in neonates and children4 5

  • Infections: TORCH infections, hepatitis viruses and EBV and malaria.

  • Metabolic: galactosaemia, lipid storage disorders - eg, Gaucher's disease.

  • Neoplastic: leukaemia, lymphoma and hepatoblastoma.

  • Haematological: sickle cell anaemia and thalassaemia.

  • Cardiovascular: congestive cardiac failure and tricuspid regurgitation.

  • Miscellaneous: schistosomiasis, toxins, sepsis, polycystic kidneys and liver.

  • Drugs: for example, antituberculous medications.

Hépatomégalie

  • With normal bilirubin: consider hepatoblastoma, metabolic diseases.

  • With raised conjugated bilirubin:

    • With splenomegaly: TORCH (TOxoplasmosis, Rubella, CMV and médicament antagoniste des récepteurs Herpes simplex) infections, sepsis and disorders of carbohydrate metabolism - eg, galactosaemia.

    • Without splenomegaly: liver tumour, choledochal cyst, biliary atresia, neonatal hepatitis.

  • With raised unconjugated bilirubin: CCF, toxins, haemolytic anaemias.

What to do if a patient has hepatomegaly

  • If unwell, may need urgent admission.

  • Full history: include recent travel, tattoos, IV drug abuse, medications as well as herbal remedies, alcohol intake and sexual history.

  • Full examination: look for stigmata of chronic liver disease, delirium tremens, lymphadenopathy, and presence of splenomegaly; digital rectal examination may be necessary.

  • Enquêtes: if the patient does not need urgent admission then request some basic investigations - eg, LFTs, FBC and film, U&Es, clotting, inflammatory markers, hepatitis screen and liver ultrasound scan. Further tests can be decided according to the results of these tests.

  • Orientation vers un spécialiste: for further assessment, diagnosis and management.

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Lectures complémentaires et références

  1. Index de Diagnostic Différentiel de French (15e Éd) 2011
  2. Médecine Clinique de Kumar et Clarke (8e éd) 2012
  3. Oxford Medical Education; Hepatomegaly, 2021
  4. Horslen S. Phenotypes of Liver Diseases in Infants, Children, and Adolescents. Diseases of the Liver in Children. 2013;107-131. Published 2013 Aug 23. doi:10.1007/978-1-4614-9005-0_6
  5. Jaan A, Rajnik M; TORCH Complex

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