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A Thrombotic Stroke Model Based On Transient Cerebral Hypoxia-ischemia
Published on: August 18, 2015
Acute ischemic stroke in a 7-month-old infant, risk factors, and diagnosis peculiarities: A case report
Lorena Elena Meliţ1, Cristina Oana Mărginean1, Iunius Simu2
1Department of Paediatrics.
Insights
Pediatric ischemic stroke, though rare, requires prompt diagnosis. This case highlights a 7-month-old infant
Area of Science:
- Pediatric Neurology
- Vascular Neurology
- Neonatal Stroke
Background:
- Ischemic stroke in children is rare, with diagnosis delays being common.
- Early recognition and intervention are critical for improved outcomes in pediatric stroke patients.
Observation:
- A 7-month-old infant presented with unilateral limb weakness and focal seizures.
- Clinical presentation included right-sided hemiparesis and focal clonic seizures affecting the hand and oral commissure.
Findings:
- Laboratory findings revealed elevated D-dimers and positive antiphospholipid antibodies (IgG anti-cardiolipin, anti-beta2 glycoprotein I).
- Genetic testing identified MTHFR C677T and A1298C heterozygote mutations.
- Brain imaging confirmed left frontal ischemic stroke, carotid artery hypoplasia, and cerebral artery agenesis.
Implications:
- Cerebral vascular malformations, obesity, and dyslipidemia can contribute to pediatric ischemic stroke.
- Multifaceted treatment including anticoagulation, antiplatelet therapy, and supportive care led to significant neurological improvement.
Introduction:
Ischemic stroke is an extremely rare disorder in children. The timely diagnosis is essential for the outcome of these children, but unfortunately, delays in diagnosis occur frequently.
Patient Concerns:
We report the case of a 7-month-old infant admitted in our clinic for limited movements of the superior and inferior right limbs whose onset was 27 hours before with repeated clonic movements of the right hand associated with the same manifestations in the right oral commissure lasting approximately 10 seconds.
Diagnosis:
The laboratory tests revealed high D-dimers, and positive IgG anti-cardiolipin and anti-beta2 glycoproteins I antibodies, whereas the genetic profile for thrombophilia revealed heterozygote mutation in MTHFR C677T and A1298C genes. Brain imaging established the diagnosis of left frontal ischemic stroke, frontal ischemic stroke, hypoplasia of internal carotid artery, and agenesia of segment M1 of median cerebral artery and segment A1 of left anterior cerebral artery.
Intervention:
We administered low-molecular-weight heparin, antiplatelet therapy along with vasodilators and depletive treatment, wide-spectrum antibiotics, and anticonvulsant therapy.
Outcome:
The neurological deficit was greatly improved, especially in the inferior limb after 6 month from the incident of stroke, and all laboratory parameters were within normal limits including the antibodies mentioned above.
Conclusion:
Cerebral vascular malformation, excessive weight, and altered lipid profiles contributed to the development of acute ischemic stroke in our patient.
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