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1.
J Neurosurg ; 120(3): 639-44, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24405074

ABSTRACT

OBJECT: Despite its long-reported successful record, with almost 60 years of clinical use, the technical complexity regarding the placement of stereoelectroencephalography (SEEG) depth electrodes may have contributed to the limited widespread application of the technique in centers outside Europe. The authors report on a simplified and novel SEEG surgical technique in the extraoperative mapping of refractory focal epilepsy. METHODS: The proposed technique was applied in patients with medically refractory focal epilepsy. Data regarding general demographic information, method of electrode implantation, time of implantation, number of implanted electrodes, seizure outcome after SEEG-guided resections, and complications were prospectively collected. RESULTS: From March 2009 to April 2012, 122 patients underwent SEEG depth electrode implantation at the Cleveland Clinic Epilepsy Center in which the authors' technique was used. There were 65 male and 57 female patients whose mean age was 33 years (range 5-68 years). The group included 21 pediatric patients (younger than 18 years). Planning and implantations were performed in a single stage. The time for planning was, on average, 33 minutes (range 20-47 minutes), and the time for implantation was, on average, 107 minutes (range 47-150 minutes). Complications related to the SEEG technique were observed in 3 patients. The calculated risk of complications per electrode was 0.18%. The seizure-free rate after SEEG-guided resections was 62% in a mean follow-up period of 12 months. CONCLUSIONS: The authors report on a safe, simplified, and less time-consuming method of SEEG depth electrode implantation, using standard and widely available surgical tools, making the technique a reasonable option for extraoperative monitoring of patients with medically intractable epilepsy in centers lacking the Talairach stereotactic armamentarium.


Subject(s)
Brain Mapping/standards , Electrodes, Implanted/standards , Electroencephalography/standards , Epilepsies, Partial/diagnosis , Epilepsies, Partial/surgery , Stereotaxic Techniques/standards , Adolescent , Adult , Aged , Brain Mapping/instrumentation , Brain Mapping/methods , Child , Child, Preschool , Electrodes, Implanted/adverse effects , Electroencephalography/adverse effects , Electroencephalography/methods , Epilepsies, Partial/physiopathology , Female , Humans , Male , Middle Aged , Postoperative Complications/epidemiology , Prospective Studies , Reproducibility of Results , Risk Factors , Stereotaxic Techniques/adverse effects , Stereotaxic Techniques/instrumentation , Young Adult
2.
World Neurosurg ; 76(5): 478.e7-478.e11, 2011 Nov.
Article in English | MEDLINE | ID: mdl-22152584

ABSTRACT

OBJECTIVE: To present the unusual finding of a lumbar intradural carcinoid metastasis in a 67-year-old man with a primary thymic carcinoid diagnosed 16 years before presentation. METHODS: The history and imaging findings of this patient are presented, and the literature is reviewed. RESULTS: Only three patients with intradural carcinoid tumors, including the one described here, have been reported. In each case, the tumor was discovered in the lumbar region. All patients were treated with surgery. The clinical behavior of metastatic carcinoid in the central nervous system (CNS) and the treatment rationale are also described. CONCLUSIONS: Carcinoid tumor metastases are rarely identified in the CNS even in patients with advanced metastatic disease.


Subject(s)
Carcinoid Tumor/secondary , Dura Mater/pathology , Lumbar Vertebrae/pathology , Spinal Neoplasms/secondary , Thymus Neoplasms/pathology , Aged , Carcinoid Tumor/therapy , Dura Mater/surgery , Fatal Outcome , Humans , Lumbar Vertebrae/surgery , Male , Spinal Neoplasms/therapy , Thymus Neoplasms/therapy
3.
J Neurointerv Surg ; 3(3): 300-3, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21990848

ABSTRACT

INTRODUCTION: Intracranial dural arteriovenous fistulas (dAVFs) with perimedullary drainage are an uncommon but well-recognized lesion that can lead to spinal cord edema. The authors present a case of a foramen magnum dAVF with unilateral arterial supply from the ascending pharyngeal artery. PRESENTATION: A 49-year-old male presented with a 1-year history of slowly progressive lower extremity weakness and underwent a two-level cervical corpectomy for presumed spondylotic myelopathy. On further workup, he was found to have a dAVF arising from the ascending pharyngeal artery. INTERVENTION: Selective angiography revealed the origin of the neuromeningeal trunk, which was proximal to the arteriovenous fistula. The microcatheter was advanced into the neuromeningeal trunk past the origin of the inferior tympanic artery and origin of the hypoglossal artery. A 4×7 mm Hyperform balloon (EV3, Irvine, California, USA) was then delivered past the origin of the vessel supplying the skull base cranial nerves, but proximal to the microcatheter tip. The balloon was inflated and Onyx embolization was employed to obliterate the fistula with controlled penetration. The patient showed immediate postprocedural improvement in motor function. DISCUSSION: Embolization of branches of the ascending pharyngeal artery carries risks of inadvertent embolization of branches of the neuromeningeal trunk as well as the risk for extracranial to intracranial anastamoses. An awareness of the highly variable anatomy of the ascending pharyngeal artery is necessary for the safe treatment of lesions supplied by this artery. This is, to the authors' knowledge, the first report of balloon-augmented embolization of an arteriovenous fistula arising from the neuromeningeal trunk.


Subject(s)
Balloon Occlusion/methods , Central Nervous System Vascular Malformations/therapy , Dimethyl Sulfoxide/therapeutic use , Polyvinyls/therapeutic use , Angiography , Arteries/abnormalities , Central Nervous System Vascular Malformations/diagnostic imaging , Embolization, Therapeutic/methods , Humans , Male , Middle Aged , Pharynx/blood supply
4.
Cleve Clin J Med ; 75(4): 311-5, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18491438

ABSTRACT

The symptoms of spinal arachnoid cysts are variable and nonspecific, so they are commonly misdiagnosed. Often the cysts are discovered incidentally on magnetic resonance imaging (MRI). If they cause no symptoms, no treatment is warranted regardless of the size of the cyst. Cysts that cause symptoms from mechanical compression of the spinal cord are best evaluated with MRI and surgically excised if possible.


Subject(s)
Arachnoid Cysts/diagnosis , Spinal Cord Compression/diagnosis , Spinal Cord/pathology , Arachnoid Cysts/complications , Humans , Magnetic Resonance Imaging/instrumentation , Myelography , Spinal Cord Compression/etiology , Tomography, Emission-Computed/instrumentation
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