The liver is one of the most frequently damaged organs in blunt trauma, and liver trauma is associated with a significant mortality rate.
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Epidemiology
In blunt abdominal trauma, the liver is injured ~5% (range 1-10%) of the time 1,3.
Clinical presentation
Patients can present with right upper quadrant pain, right shoulder tip pain (from diaphragmatic irritation), hypotension, and shock 3.
Pathology
Aetiology
The mechanism for liver trauma can be blunt (e.g. motor vehicle collision, fall, direct blow, etc.) or penetrating trauma (e.g. gunshot, stabbing). It can also be iatrogenic (e.g. percutaneous liver biopsy, operative injury).
Types
Most (~80%) of liver injuries are minor (grades I to III - see AAST grading). There are a range of injuries ref:
laceration: most common
haematoma: subcapsular or intraparenchymal
active bleeding
major hepatic vein injury
arteriovenous (AV) fistula
Associations
Approximately 80% of liver injuries are associated with other abdominal injuries 1,3.
Within the liver:
lacerations that involve a hepatic vein are associated with increased risk of arterial injury and need for operative management 8
although not an injury, periportal oedema can be seen associated with liver injuries as patients with higher-grade injuries will have received aggressive fluid resuscitation
lacerations that extend to the porta hepatis increase the risk of bile duct injuries, particularly delayed biliary complications 8
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bile duct injuries are more common in 9
higher grade injuries
central injuries, that is injuries that are close to the IVC
penetrating trauma, compared with blunt trauma
Outside the liver (known as secondary signs) ref:
lacerations that extend to the bare area can be associated with retroperitoneal haemorrhage or adrenal haematoma
right lower lobe pulmonary contusion/laceration
right-sided rib fractures
right renal injury
Markers
Elevated liver transaminases (ALT/AST) are 100% specific and ~93% sensitive in predicting liver injuries 4,6.
Radiographic features
CT
CT is the investigation of choice for evaluating liver trauma. It is ~95% sensitive and 99% specific for detecting liver injuries 5.
lacerations appear as irregular linear/branching areas of hypoattenuation
chronic haematomas appear as a hypodensity between the liver and its capsule (and can be differentiated from intra-peritoneal haematoma as these distort the liver architecture) or can be intraparenchymal
acute haematomas/haemorrhage are typically hyperdense (40-60 HU) compared to normal liver parenchyma
muscular diaphragmatic slips may simulate a peripheral laceration but are smoother, non-branching and of muscle density when compared to a laceration
If the liver is diffusely hypoattenuating, such as seen in steatosis, lacerations and haematomata may be more subtle to diagnose 8. Secondary signs should help.
See the main article liver injury grading for more details.
Hepatic scintigraphy
Scintigraphy, such as that using Tc-99m mebrofenin or disofenin, is the most commonly used test for the diagnosis of bile leaks 9. A contained leak will demonstrate an extrabiliary focus of radiotracer which remains stable in size and morphology during all the phases of the study. A free intraperitoneal bile leak will demonstrate an extraluminal collection of radiotracer in the peritoneal cavity that varies or increases in time 9.
Differential diagnosis
Several mimics of liver lacerations and haematomata exist, and include 8:
focal fat infiltration
unenhanced aberrant portal or hepatic veins
congenital fissures and clefts: typically fat density, and in usual locations
diaphragmatic slips or eventration: identifiable on coronal images
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pre-existing liver lesions
cysts
Treatment and prognosis
Most (>80%) of liver injuries can be treated non-surgically, and blunt trauma relies on haemodynamic stability rather than a grade of injury 4-5. There is a significant mortality rate of ~8% (range 4.1-11.7%) associated with liver trauma 1. Complications are reported in ~20% of cases of non-operatively treated liver trauma 7:
bile duct injury leading to complications such as bile peritonitis or biloma
rebleeding/delayed or secondary haemorrhage
intra-abdominal abscess formation
liver necrosis