Hepatomegaly
| Hepatomegaly | |
|---|---|
Computerized tomography of hepatomegaly
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| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| ICD-10 | R16..0 |
| ICD-9-CM | 789.1 |
| MedlinePlus | 003275 |
| Patient UK | Hepatomegaly |
Hepatomegaly is the condition of having an enlarged liver. It is a non-specific medical sign having many causes, which can broadly be broken down into infection, direct toxicity, hepatic tumours, or metabolic disorder. Often, hepatomegaly will present as an abdominal mass. Depending on the cause, it may sometimes present along with jaundice.
Contents
Causes
Infective
- Glandular fever (Infectious mononucleosis) This is caused by the Epstein-Barr virus (EBV). A similar condition (pseudoglandular fever) may be caused by cytomegalovirus (CMV).
- Hepatitis (Although not all hepatitis viruses cause hepatomegaly)
- Liver abscess (pyogenic abscess and amoebic abscess)
- Malaria
- Amoeba infections
- Hydatid cyst
- Leptospirosis
- Actinomycosis
Neoplastic
- Metastatic tumours secondary to spread from cancer in other organs (most common)
- Hemangiomas
- Hepatocellular carcinoma
- Myeloma
- Leukemia
- Lymphoma
- hepatoma
Cirrhotic
- Portal
- Biliary
- Cardio
- Haemochromatosis
Metabolic
- Fatty infiltration
- Lysosomal acid lipase deficiency, also known as Wolman disease or cholesteryl ester storage disease
- Amyloidosis
- Gaucher's disease
- Niemann Pick disease
- Von Gierke disease (Glycogen Storage Disease type 1)
- Glycogen Storage Disease types III, VI and IX
Drugs and toxins
Congenital
- Hemolytic anemia
- Riedel's lobe is an extended, tongue-like, right lobe of the liver. It is not pathological; it is a normal anatomical variant and may extend into the pelvis. It is often mistaken for a distended gall bladder or liver tumour.
- Polycystic disease
- Cori's disease
Others
- Budd–Chiari syndrome
- Hunter syndrome
- Zellweger's syndrome
- Carnitine palmitoyltransferase I deficiency
- Right ventricular failure
- Granulomatous: Sarcoidosis
- Glycogen storage disease type II
Diagnosis
A suspicion of hepatomegaly indicates a thorough medical history and physical examination, wherein the latter typically includes an increased liver span. Blood tests should be done, importantly liver-function series, which will give a good impression of the patient's broad metabolic picture.
An ultrasound of the liver can reliably detect a dilated biliary-duct system, which helps distinguish parenchymal liver disease from extrahepatic bile-duct obstruction. Ultrasound can also detect the characteristic texture of a cirrhotic liver, and can guide fine-needle aspiration of cysts, abscesses and tumours.
Computed tomography or (computerized tomography) (CT) can help to obtain more accurate anatomical information, and is unaffected by obesity or the presence of bowel gases.
