Case Report: We report the case of a nine-year-old child with a cervical medullary arteriovenous malformation (AVM), revealed by total paraplegia, whose regression started during steroid therapy, before embolization.
Conclusion: The frequency of AVM's spontaneous favorable outcome is unknown but should not be underestimated. It might be improved by steroids.
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http://dx.doi.org/10.1016/s0929-693x(00)00284-0 | DOI Listing |
Acta Neurochir (Wien)
December 2024
Department of Neurosurgery, National Center for Neurological Disorders, Huashan Hospital, Shanghai Medical College, Fudan University, No. 12 Wulumuqi Zhong Road, Shanghai, 200040, China.
Background: Craniocervical junction (CCJ) dural arteriovenous fistulas (DAVFs) represent a rare yet critical vascular anomaly that may result in significant neurological impairments.
Method: We report the case of a 52-year-old male with a history of medullary hemorrhage who underwent surgical intervention for a left CCJ DAVF. Through comprehensive surgical planning and meticulous intraoperative monitoring, multiple feeders of the DAVF were safely coagulated and transected, with successful DAVF obliteration confirmed by intraoperative angiography.
Surg Neurol Int
November 2024
Department of Neurosurgery, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Background: Arteriovenous malformation (AVM) and developmental venous anomaly (DVA) rarely coexist. Developing a surgical strategy to treat this co-occurrence is difficult due to the unclear pathogenesis. We report the use of super-selective digital subtraction angiography (DSA) and Three-dimensional (3D) rotational digital subtraction venography (DSV) to develop a surgical strategy for complex AVM draining into a DVA.
View Article and Find Full Text PDFEinstein (Sao Paulo)
November 2024
Laboratory of Molecular and Cellular Biology (LIM15), Department of Neurology, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.
J Neuroendovasc Ther
September 2024
Department of Neurosurgery, Dokkyo Medical University, Shimotsugagun, Tochigi, Japan.
Objective: We describe two cases of myelopathy onset due to intracranial dural arteriovenous fistulas (DAVFs) and present a literature review.
Case Presentation: (Case 1) A 44-year-old man with subacute onset myelopathy underwent an MRI and DSA. MRI showed T2-hyperintensity from the medulla oblongata to the cervical spinal cord with vascular flow voids, suggestive of a spinal DAVF.
Neurology
December 2024
From the Department of Neurology (M.B., G.M., F.C., S.S., K.O.R., C.F.), Mater Misericordiae University Hospital, Dublin; and Department of Neuroradiology (D.B., P.N.), Beaumont Hospital, Dublin, Ireland.
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