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Ruptured dissecting vertebrobasilar aneurysm in childhood: what is the therapeutic strategy?
Michele Rizzi1, Alessandro De Benedictis, Carlo Efisio Marras
1Division of Neurosurgery, Fondazione IRCCS Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, University of Milan, Milan, Italy. michele.rizzi@live.it
Insights
Endovascular treatment effectively managed a dissecting vertebrobasilar aneurysm (DVBA) in a pediatric patient with subarachnoid hemorrhage. The procedure preserved critical blood flow, leading to a stable recovery without neurological deficits.
Area of Science:
- Pediatric neurosurgery
- Vascular neurology
- Interventional neuroradiology
Background:
- Dissecting vertebrobasilar aneurysms (DVBA) are rare in children but present a high mortality risk when causing subarachnoid hemorrhage.
- Prompt treatment is crucial for pediatric DVBA with acute subarachnoid hemorrhage.
Observation:
- An 8-year-old female presented with sudden severe headache, vomiting, and loss of consciousness.
- CT revealed subarachnoid hemorrhage; MR angiography indicated a vertebrobasilar junction aneurysm with mass effect.
- Intracranial angiography confirmed the DVBA and showed significant anterior cerebral circulation revascularization.
Findings:
- Endovascular treatment, specifically occlusion of both vertebral arteries while preserving the left posterior inferior cerebellar artery, was successfully performed.
- The patient experienced no neurological deficits post-embolization and remained clinically stable at 18 months.
Implications:
- Parent vessel deconstruction via endovascular techniques is a viable option for pediatric DVBA.
- This approach is suitable when collateral circulation is adequate and vital brain structures are not compromised.
Background/Aims:
Pediatric aneurysms are rare, accounting for 0.5-4.6% of all intracranial aneurysms. Dissecting vertebrobasilar aneurysms (DVBA) are more frequently observed among children than adults. Cases acutely presenting with subarachnoid hemorrhage need a prompt treatment because of the higher mortality related to untreated cases. Options for an active DVBA management depend on the features of the malformation and include endovascular and surgical approaches.
Methods:
We refer to an 8-year-old healthy female, who presented with a sudden severe headache and vomit, followed by a half-hour loss of consciousness. A CT scan revealed subarachnoid hemorrhage, and brain MR angiography showed a lesion with mass effect on bulbar structures, suggestive of an aneurysm of the vertebrobasilar junction. The intracranial angiography confirmed this diagnosis and showed a relevant revascularization coming from the anterior cerebral circulation.
Results:
Endovascular treatment was considered as a suitable option and occlusion of both vertebral arteries, saving the left posterior inferior cerebellar artery, was performed. No neurological deficits appeared after embolization, and the patient was clinically stable at 18 months of follow-up.
Conclusion:
In the 'stent era', parent vessel deconstruction throughout endovascular balloon or coil occlusion could be considered in patients with a sound collateral circulation and when cerebellar hemisphere and encephalic trunk feeding is not compromised.
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