Isolated cystic lesion of the callosal genu after traumatic brain injury
Toru Kato1, Akihisa Okumura, Takeshi Tsuji
1Department of Pediatrics, Okazaki City Hospital, Okazaki, Japan. kato-jes@umin.ac.jp
Insights
A rare cystic lesion in the callosal genu of an infant was identified as a unique form of traumatic axonal injury (TAI). This finding highlights the importance of recognizing unusual presentations of TAI in children following traumatic brain injury (TBI).
Area of Science:
- Pediatric neurology
- Neuroimaging
- Traumatic brain injury research
Background:
- Traumatic axonal injury (TAI) commonly affects the corpus callosum.
- Previous literature lacks reports of isolated cystic lesions in the callosal genu as a TAI manifestation.
- Infants are particularly vulnerable to TAI due to developing brain structures.
Observation:
- A 17-month-old infant presented with an isolated cystic lesion in the callosal genu after a traffic accident.
- Initial computed tomography scans were normal; however, magnetic resonance imaging revealed a cystic cavity in the callosal genu after 3 months.
- The lesion demonstrated a decrease in size over a 16-month follow-up period.
Findings:
- The observed isolated cystic lesion in the callosal genu represents a unique presentation of TAI in an infant.
- Neuroimaging findings suggest this cystic cavity is a potential sequela of traumatic brain injury (TBI).
- The lesion's evolution, including size reduction, provides insights into the natural course of TAI in pediatric cases.
Implications:
- This case expands the understanding of TAI manifestations in infants, particularly the potential for isolated cystic lesions in the callosal genu.
- Clinicians should consider TAI when encountering such cystic lesions in children with a history of TBI.
- Further research is warranted to elucidate the pathogenesis and long-term outcomes of this specific TAI presentation in pediatric populations.
Abstract:
We report the case of a 17-month-old infant who developed an isolated cystic lesion of the callosal genu as a unique lesion of traumatic axonal injury (TAI). Although one of the most common sites of TAI is the corpus callosum, there have been no reports describing the lesion seen in our patient. Brain computed tomography findings were normal on the day of the traffic accident. After 3 months, brain magnetic resonance imaging showed an isolated cystic lesion of the callosal genu that had the appearance of a cystic cavity. This lesion decreased in size 16 months later. The neuroimaging findings of this patient suggest that an isolated cystic lesion of the callosal genu could appear as a unique form of TAI in infants after traumatic brain injury (TBI), but it is nevertheless important to attend to such lesions in children with TBI.
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