98%
921
2 minutes
20
Arteriovenous fistulas of the filum terminale are rare vascular malformations that predominantly affect males and can present with various neurological symptoms. In this study, we indexed previously published cases of filum terminale arteriovenous fistulas demonstrating that endovascular and microsurgical management are both proven to be appropriate and successful treatment modalities with low complication rates. Endovascular treatment is far less invasive; however, it is associated with higher failure rates, which need to be managed surgically. In this case, we report a 64-year-old male patient who presented with lower back pain and bilateral lower extremity weakness. He was found to have a filum terminal arteriovenous fistula causing thoracolumbar spinal cord edema. Following a failed attempt of endovascular embolization complicated by declining neuromonitoring signals, open microsurgical obliteration of the lesion was successfully performed. While endovascular management of filum terminale arteriovenous fistulas is a viable and successful treatment modality in select cases, surgeons should be prepared to manage these cases with an open microsurgical approach should embolization fail or become unsafe. Proper radiologic characterization of the lesion and accurate localization of the location of the fistula are requisites to a safe and successful obliteration of these lesions.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11697502 | PMC |
http://dx.doi.org/10.7759/cureus.75083 | DOI Listing |
Childs Nerv Syst
September 2025
Department of Orthopedics, The Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Objective: To analyze the filum terminale (FT) of children with tethered cord syndrome (TCS) and aborted fetuses without neurological disorders in order to investigate the expression of significantly differentially expressed proteins in the FT under both pathological and physiological conditions.
Methods: According to the inclusion and exclusion criteria, 35 FT samples were selected, and the samples were subjected to immunohistochemistry and H&E staining. The data were analyzed using one-way analysis of variance, and P < 0.
Cureus
August 2025
Department of Neurosurgery, Faculty of Medicine, Medical University of Plovdiv, Plovdiv, BGR.
This report presents the case of a 36-year-old man complaining of chronic low back pain and numbness along the posterolateral surface of the right leg. Magnetic resonance imaging (MRI) revealed a disc degeneration and protrusion at the L-S level and an extensive fluid-equivalent formation with a craniocaudal dimension of 8 cm at the S-S level. Initially, due to the minimal clinical complaints, the cyst was considered asymptomatic.
View Article and Find Full Text PDFAim: This study aims to assess the incidence of retethering in patients who underwent surgery for tethered cord in our clinic.
Material And Methods: We included patients who underwent surgical intervention for tethered cord in our clinic between 2010 and 2020 and were subsequently diagnosed with retethering during follow-up. Only those with available postoperative clinical follow-up data were included.
J CME
September 2025
AO Foundation, AO Education Institute, Davos Platz, Switzerland.
Integrating patient perspectives in medical education is increasingly recognised as critical for patient-centred care. However, many continuing professional development (CPD) programmes - particularly in surgical education - lack a structured approach to involve the patient perspective. This study explored faculty awareness, exposure, engagement and perceived barriers to integrating patient perspectives in surgeon education.
View Article and Find Full Text PDFCureus
August 2025
Department of Research for Spine and Spinal Surgery, Fukushima Medical University, Fukushima, JPN.
Dural tears are a well-known complication of spinal surgery. While most occur intraoperatively and are promptly identified, some are overlooked or develop postoperatively. Delayed-onset dural tears are relatively rare but can result in significant neurological complications, including cauda equina syndrome (CES).
View Article and Find Full Text PDF