Infantile traumatic brain injury with a biphasic clinical course and late reduced diffusion (TBIRD)

Trauma
Pediatric diseases

General description

Infantile traumatic brain injury with a biphasic clinical course and late reduced diffusion (TBIRD) is a condition observed in infants after head trauma, including cases of abuse. It presents with clinical and imaging findings similar to Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD). However, unlike AESD, TBIRD is often associated with acute subdural hematoma in the early stages, which is a distinguishing feature.

TBIRD typically follows a biphasic course, with bright tree appearance (BTA) emerging around days three to six and severe brain atrophy developing in the chronic phase. The pathophysiology of TBIRD involves excitotoxicity mediated by glutamate, leading to rapid brain edema after late seizures, often resulting in a poor prognosis.

Differential diagnosis

While both TBIRD and AESD exhibit biphasic progression and BTA, TBIRD is linked to head trauma, necessitating careful differentiation between the two. AESD is caused by infections and usually presents with fever at onset, but fever can occasionally be seen in TBIRD cases as well, making diagnosis challenging. The presence of acute subdural hematoma and differences in BTA distribution—frontal predominance in AESD versus occipital involvement with asymmetry in TBIRD—are key factors in distinguishing between these conditions.

Subdural hematoma

  • Subdural space
Plain CT
Blood attenuation
High attenuation
T1WI
Hyperintensity
FLAIR
Hyperintensity
T2*WI
Hypointensity
DWI
Hyperintensity

Bright tree appearance

  • Cerebrum
    Frontal lobe
    Cerebral white matter
    Subcortical white matter
    U-fiber
  • Cerebrum
    Parietal lobe
    Cerebral white matter
    Subcortical white matter
    U-fiber
Asymmetric
Unilateral
Linear
T2WI
Hyperintensity
FLAIR
Hyperintensity
DWI
Hyperintensity
ADC
Hypointensity

T2WI and FLAIR reveal asymmetric linear hyperintensity involving the subcortical U-fibers, predominantly affecting the frontal and parietal lobes, while sparing the precentral and postcentral gyri. Unlike AESD, the 'bright tree appearance' in TBIRD is more pronounced in the parietal lobe.