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Severe Cerebral Vasospasm and Childhood Arterial Ischemic Stroke After Intrathecal Cytarabine
Daniel Tibussek1, Rungrote Natesirinilkul2, Lisa R Sun3
1Division of Neurology, Department of Pediatrics, Hospital for Sick Children, Toronto, Canada; Department of General Pediatrics, Neonatology and Pediatric Cardiology, University Children's Hospital, Heinrich-Heine University, Düsseldorf, Germany; daniel.tibussek@gmx.net.
Insights
Intrathecal cytarabine can cause serious neurological issues like cerebral vasospasm and stroke in children with acute lymphoblastic leukemia (ALL). Early MRI and MRA are recommended for any child experiencing neurological symptoms after this treatment.
Area of Science:
- Pediatric Neurology
- Neuro-oncology
- Pharmacology
Background:
- Intrathecal (IT) cytarabine is a common chemotherapy for acute lymphoblastic leukemia (ALL).
- Neurological adverse events following IT cytarabine are known but can be severe.
- Cerebral vasospasm and arterial ischemic strokes (AIS) are rare but serious potential complications.
Abstract:
We report on 2 patients who developed widespread cerebral vasospasm and arterial ischemic strokes (AIS) after application of intrathecal (IT) cytarabine. In a 3-year-old child with acute lymphoblastic leukemia (ALL), left leg weakness, hyperreflexia, and clonus were noted 4 days after her first dose of IT cytarabine during the induction phase of her chemotherapy. Cerebral MRI revealed multiple acute cerebral ischemic infarcts and widespread cerebral vasospasm. A 5-year-old girl complained of right arm and leg pain and began limping 11 days after IT cytarabine. Symptoms progressed to right dense hemiplegia, left gaze deviation, headache, and speech arrest. MRI revealed 2 large cortical areas of diffusion restriction in the right frontal and left parietal lobes. Cerebral magnetic resonance angiography (MRA) showed irregular narrowing affecting much of the intracranial arterial circulation. Although the first child fully recovered from her neurologic symptoms, the second patient had persistent hemiplegia on follow-up. Including this report, there are now 4 pediatric ALL cases of severe cerebral vasospasm and AIS in the context of IT cytarabine administration, strongly suggesting a true association. Differential diagnosis and management issues are discussed. Along with the more widespread use of MRI and MRA, the true frequency of this severe adverse effect will become clearer in future. For any child with neurologic symptoms within hours or days of receiving IT cytarabine, a low threshold for cerebral imaging with MRI and MRA is recommended.
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