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dc.contributor.authorYuliatri, Nia-
dc.contributor.authorAyke Widjaya, Ingrid-
dc.contributor.authorAditiara Wibawa, Gibran-
dc.contributor.authorHarlyjoy, Alphadenti-
dc.contributor.authorSatyanegara, Satyanegara-
dc.date.accessioned2025-02-21T04:46:35Z-
dc.date.available2025-02-21T04:46:35Z-
dc.date.issued2024-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/9706-
dc.description.abstractIntracranial dural arteriovenous fistula (DAVF) that drains into spinal perimedullary veins can generate longitudinally extensive transverse myelitis (LETM)-like lesion, which often represents a significant diagnostic and therapeutic challenge. This is a case report of a 50-year-old male referred with all extremity weaknesses. Despite receiving high-dose intravenous steroids for suspected myelitis, no improvement was recorded. Spinal imaging showed abnormal hyperintensity extending from the T6 vertebral level to the medulla, and a flow void lesion from the cervicomedullary junction up to the L3 level. Angiography confirmed a Cognard type V spinal DAVF, which was treated with transarterial embolization of the feeding vessel. Follow-up angiography showed complete occlusion of the fistula without any backflow. Flow voids are no longer visible on MRI conducted 3 weeks post-procedure. Unfamiliarity with these disorders often leads to delays in diagnosis and treatment. Therefore, it is essential to consider intracranial DAVF as a differential diagnosis for LETM-like lesions. KEYWORDS endovascular procedures, dural arteriovenous fistula, transverse myelitisen_US
dc.subjectendovascular procedures, dural arteriovenous fistula, transverse myelitisen_US
dc.titleIntracranial dural arteriovenous fistula presenting like longitudinally extensive transverse myelitisen_US
dc.typeArticleen_US
Appears in Collections:VOL 33 NO 4 (2024)

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