Posterior Spinal Artery Infarct due to Patent Foramen Ovale
| Autor: | Francesco Federico, Mariapia Prontera, Maurizio Giorelli, V. Lucivero, Angela Fraddosio, Angelica Tinelli, M. Petruzzellis |
|---|---|
| Rok vydání: | 2010 |
| Předmět: |
medicine.medical_specialty
Ticlopidine Anterior spinal artery Foramen Ovale Patent Infarction Disease-Free Survival Posterior spinal artery Myelopathy Paradoxical embolism medicine.artery medicine Humans Orthopedics and Sports Medicine Physical Therapy Modalities Dysesthesia business.industry Middle Aged medicine.disease Magnetic Resonance Imaging Surgery Treatment Outcome Spinal Cord Patent foramen ovale Female Neurology (clinical) medicine.symptom business medicine.drug |
| Zdroj: | Spine. 35:E155-E158 |
| ISSN: | 0362-2436 |
| Popis: | Study design Case report. Objective To report the first case of posterior spinal artery (PSA) infarct due to patent foramen ovale (PFO). Summary of background data Infarct in the territories of PSA are very rare: till now 38 cases are reported in the literature. Moreover only 1 case of spinal cord infarction was attributed to paradoxical embolism through PFO, but in the anterior spinal artery territory. Methods A 60-year-old woman was hospitalized for sudden numbness of the right leg. Neurologic examination revealed right leg mild paresis and loss of proprioception and dysesthesia at T11. Spine-MRI showed T5-T7 posterolateral cord ischemia. Transesophageal echocardiography disclosed a PFO with severe right-left shunt confirmed by transcranial Doppler. Results During the hospitalization she was treated with oral-500 mg ticlopidine, because of a mild allergic reaction to acetylsalicylic acid. No steroids were administrated. Physiotherapy was performed daily. Motor and urinary symptoms disappeared in 20 days. At 1-month clinical follow-up only suspended dysesthesia on the right side was present. At 3 months follow-up spine-MRI showed no signal abnormalities within the spinal cord but the patient still complained of dysesthesia. The therapy was changed to oral 75 mg clopidogrel, cause of leucopoenia. At 1-year follow-up dysesthesia was still present, but less complaining and no recurrence and adverse effect due to clopidogrel therapy were reported. Conclusion This report describe a case of acute nontraumatic myelopathy. At 4 days after onset, PSA infarct was diagnosed on the basis of neurologic findings and MR images. After extensive diagnostic work-up, we were able to identify only PFO, so it was the first case of PSA due to probable paradoxical embolism. The patient was treated with antiplatelet therapy with good recovery and no recurrence at 1-year follow-up. |
| Databáze: | OpenAIRE |
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