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Delayed presentation of a pediatric giant traumatic pseudoaneurysm mimicking a brain tumor: a case report
Anıl Erol1, Cihat Karagöz2, Larisa Andrada Ay3
1Faculty of Medicine, Department of Neurosurgery, Ege University, Izmir, Turkey. anilerolhitit19@gmail.com.
Insights
Giant intracranial pseudoaneurysms (IPAs) in children are rare and can mimic tumors. This case shows successful endovascular treatment for a pediatric IPA presenting years after head trauma.
Area of Science:
- Pediatric Neurology
- Vascular Neurosurgery
- Neuroradiology
Background:
- Intracranial pseudoaneurysms (IPAs) are rare, comprising <1% of intracranial aneurysms.
- Pediatric IPAs carry high morbidity/mortality risks and giant forms can mimic tumors.
- Thrombosed IPAs present diagnostic challenges due to heterogeneous imaging features.
Purpose of the Study:
- To report a rare case of a giant intracranial pseudoaneurysm in a child.
- To highlight diagnostic challenges and successful treatment of pediatric IPAs.
- To emphasize the importance of advanced imaging in diagnosing pediatric vascular lesions.
Main Methods:
- Case report of an 11-year-old boy with a history of head trauma.
- Initial neuroimaging revealed a suspected giant cystic-solid tumor.
- Diagnosis confirmed via angiography, followed by endovascular coil embolization.
Main Results:
- A giant pseudoaneurysm of the right anterior cerebral artery was identified.
- The lesion mimicked a neoplastic lesion on initial imaging.
- Successful endovascular coil embolization was performed.
Conclusions:
- Giant pediatric IPAs can present years after head trauma and mimic tumors.
- Thorough preoperative imaging review and vascular studies are crucial for diagnosis.
- Endovascular treatment is a viable option for pediatric IPAs.
Abstract:
Intracranial pseudoaneurysms (IPAs) account for less than 1% of all intracranial aneurysms, yet they have been reported more frequently in the pediatric population, carrying a high risk of morbidity and mortality. Giant IPAs in children are extremely rare and may mimic intracranial tumors on imaging, making diagnosis challenging. Thrombosed pseudoaneurysms, in particular, can resemble neoplastic lesions due to their heterogeneous appearance and contrast enhancement patterns. This report describes the case of an 11-year-old boy with a history of head trauma five years earlier, who was admitted after developing a seizure following severe headache. Neuroimaging revealed a giant cystic-solid lesion in the frontal lobe, initially suspected to be a tumor. Surgery was planned, but intraoperatively the lesion was found to be vascular. Subsequent angiography demonstrated a giant pseudoaneurysm arising from the pericallosal branch of the right anterior cerebral artery. The patient was successfully treated with endovascular coil embolization. This case highlights that giant pseudoaneurysms can present years after head trauma in children and may radiologically mimic tumors. Careful preoperative imaging review and advanced vascular studies, when necessary, are essential for timely and accurate diagnosis. Additional reports in the literature will further improve our understanding of the clinical and radiological features of pediatric pseudoaneurysms and guide treatment selection.
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