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Case report: neuroimaging analysis of pediatric ADHD-related symptoms secondary to hypoxic brain injury
1a Department of Psychiatry and Human Behavior, University of California , Irvine , CA , USA.
Insights
Hypoxic brain injury in a child was misdiagnosed as attention deficit hyperactivity disorder (ADHD). Advanced neuroimaging revealed unique brain alterations, suggesting ADHD secondary to injury, not heritability.
Area of Science:
- Neuroscience
- Pediatric Neurology
- Radiology
Background:
- A pediatric patient presented with symptoms later diagnosed as attention deficit hyperactivity disorder (ADHD).
- The patient had a history of partial internal carotid occlusion and asphyxiation at age two, leading to hypoxic brain injury.
Observation:
- Advanced neuroimaging techniques including diffusion tensor imaging (DTI), positron emission tomography (PET), and quantitative volumetrics (QV) MRI were employed nine years post-incident.
- DTI revealed significantly reduced fractional anisotropy (FA) in key brain regions, exceeding typical ADHD-related changes.
- PET scans showed decreased metabolism in areas not characteristic of ADHD, and QV identified enlarged brain regions, including the amygdala, contrary to ADHD literature.
Findings:
- The patient's neuroimaging data presented distinct patterns inconsistent with primary ADHD.
- Specific reductions in FA and altered metabolic activity were observed in the anterior corpus callosum, internal capsule, hippocampus, orbitofrontal cortex, anterior cingulate, insular cortex, and striatum.
- Enlargement of the amygdala was noted, contrasting with typical ADHD findings.
Implications:
- The unique neuroimaging profile strongly suggests the patient's ADHD symptoms are a sequela of secondary hypoxic brain injury rather than primary heritability.
- This case highlights the importance of considering secondary causes for ADHD-like symptoms, especially with a history of brain insult.
- The findings underscore the utility of advanced neuroimaging in differentiating primary ADHD from ADHD secondary to brain injury.
Abstract:
A 2-year-old male pediatric patient experienced a partial occlusion of the internal carotid and subsequent asphyxiation resulting in hypoxic brain injury that was later misdiagnosed as primary attention deficient hyperactivity disorder (ADHD). Imaging analyses using diffusion tensor imaging (DTI), positron emission tomography (PET), and magnetic resonance imaging (MRI) quantitative volumetrics (QV) were used nine years following the incident to identify whether his development of ADHD is of a primary heritability or secondary hypoxic brain injury sequelae. The patient's DTI analysis generated decreases in fractional anisotropy (FA) values in the anterior corpus callosum, bilateral internal capsule, and hippocampus. Decreases in FA are seen in ADHD patients, but the degree of FA decrease in the patient under study is several orders of magnitude greater than in ADHD patients. Also, not normally observed in ADHD patients were decreases in the metabolism of the orbitofrontal cortex, anterior cingulate, left anterior insular cortex, and left striatum. Additionally, QV showed enlargements of various regions of the brain including the amygdala which is often cited in the literature to be reduced in ADHD patients. The diagnosis of this patient despite having non-characteristic neuroimaging data suggests a unique specificity of the hypoxic injury to the development of a secondary hypoxic brain injury caused ADHD.
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