298 results match your criteria: "Tumors of the Conus and Cauda Equina"
World Neurosurg
March 2018
Department of Neurosurgery, Hannover Medical School, Hannover, Germany; Department of Neurosurgery, Cologne Merheim Hospital, University of Witten/Herdecke, Cologne, Germany.
Background: Ependymomas are rare central nervous system tumors. Local tumor distribution in the central nervous system depends on age: among adults, ependymomas occur mostly in the spinal cord, whereas among children, intracranial manifestations are more common. To date, there are no prospective studies about treatment strategies for ependymomas.
View Article and Find Full Text PDFJ Neurosurg Spine
February 2018
1Department of Neurosurgery, Memorial Sloan Kettering Cancer Center, New York, New York; and.
Asian J Neurosurg
January 2017
Department of Neurosurgery, Liaquat National Hospital and Medical College, Karachi, Pakistan.
Intradural arachnoid cysts are a rare cause of spinal cord and nerve root compression. Primarily, they are present in the thoracic region posteriorly. We report a 25-year-old man who had an intradural arachnoid cyst at the level of conus medullaris presenting with cauda equina syndrome, which is very rare.
View Article and Find Full Text PDFActa Neurochir (Wien)
October 2017
Division of Neurosurgery, Addenbrooke's Hospital, Hills Road, Cambridge, CB2 0QQ, UK.
Introduction: Spinal bronchogenic cysts are rare findings, with only four cases of lumbar bronchogenic cysts reported in the literature. All of these bronchogenic cysts involved the conus medullaris. We present the first case of a lumbar bronchogenic cyst and arachnoid cyst arising from the cauda equina in a 68-year-old male.
View Article and Find Full Text PDFNMC Case Rep J
July 2016
Department of Neurosurgery, The Jikei University School of Medicine, Tokyo, Japan.
We present a rare case of spontaneous hemorrhage of a spinal ependymoma in the filum terminale presenting with acute cauda equina syndrome. A 16-year-old male presented with a sudden onset of severe back pain that began 10 days before hospitalization. This symptom progressed, followed by development of decreased sensation in the lower extremities, bladder dysfunction, and motor weakness that advanced to an inability to walk.
View Article and Find Full Text PDFAcad Radiol
August 2017
Department of Radiology, University of Utah Health Sciences Center, 30 North 1900 East #1A071, Salt Lake City, UT 84132-2140.
Rationale And Objectives: Emergency department (ED) patients with acute low back pain (LBP) may present with ambiguous clinical findings that pose diagnostic challenges to exclude cauda equina syndrome (CES). As a proof of concept, we aimed to determine the efficacy of a rapid lumbar spine (LS) magnetic resonance imaging (MRI) screening protocol consisting of a single 3D-T2 SPACE FS (3D-T2 Sampling Perfection with Application optimized Contrasts using different flip angle Evolution fat saturated) sequence relative to conventional LS MRI to exclude emergently treatable pathologies in this complex patient population.
Materials And Methods: LS MRI protocol including a sagittal 3D-T2 SPACE FS pulse sequence was added to the routine for ED patients presenting with acute atypical LBP over a 12-month period.
Neurosurg Rev
January 2018
Department of Neurosurgery, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka, 545-8585, Japan.
The objective of this retrospective case analysis was to evaluate the surgical impact on neurological functional recovery in cases of solitary spinal nerve sheath tumors (NSTs) originating around the epiconus, conus medullaris, or cauda equina and not associated with neurofibromatosis. This 10-year surgical study included 30 cases of spinal NSTs originating around the spine level of T12-L1 (epiconus-to-conus medullaris: Epi-CM group), and 15 cases of spinal NSTs originating below the spine level of L2 (cauda equina: CE group). A minimally invasive posterior unilateral approach was applied in 22 of 30 subjects in the Epi-CM group and in 14 of 15 subjects in the CE group.
View Article and Find Full Text PDFWorld Neurosurg
March 2017
Department of Neurosurgery, University of Tennessee Health Science Center, Memphis, Tennessee, USA; Semmes-Murphey Neurologic & Spine Institute, Memphis, Tennessee, USA. Electronic address:
Myxopapillary ependymoma (MPE) is a slow-growing tumor, occurring most often in adults. It originates from the filum terminale in the area of the conus medullaris and cauda equina and is considered a benign lesion. Despite this classification, however, recurrence after both partial and gross total resection is well known.
View Article and Find Full Text PDFSurg Neurol Int
November 2016
Department of Neurosurgery, University of Medical Sciences, Rasool Akram Hospital, Tehran, Iran.
Background: Dermoid tumors are slow growing, benign CNS lesions.
Case Description: This case study concerns a 29-year-old female with a 6-year history of lower extremity paresthesias attributed to magnetic resonance (MR)/computed tomography (CT) documented intradural dermoid tumor that extended from L1 to S1. On MR, it was hypointense on T1, hyperintense on T2, and did not enhance with gadolinium.
J Clin Diagn Res
September 2016
Senior Resident, Department of Neurosurgery, TN Medical College and BYL Nair Hospital, Mumbai, Maharashtra, India .
Introduction: One half of all central nervous system ependymomas, arise within the spinal canal and about 40% of these arise from filum terminale. The myxopapillary variant of spinal ependymoma almost exclusively occurs in the lumbosacral region and they are histologically designated as Grade I. Long term control is best achieved by gross total removal at the initial operation.
View Article and Find Full Text PDFMyxopapillary ependymoma is a benign slow-growing tumour, arising predominantly in the region of the filum terminale. It has been designated histologically as grade I neoplasm according to the 2007 WHO classification. Despite this benign character dissemination and metastasis along the cerebrospinal axis and metastasis to distant sites have occasionally been reported.
View Article and Find Full Text PDFJ Neurosurg Pediatr
October 2016
Department of Neurosurgery, Brain Research Institute, University of Niigata, Niigata City; and.
The authors report the case of a mobile spinal enterogenous cyst in a 2-year-old boy, who was admitted to the hospital several times for intermittent paraplegia. Magnetic resonance imaging and CT revealed an isolated cyst in the lumbar spinal canal. The symptoms were caused by transient myelopathy of the conus medullaris and radiculopathy of the cauda equina due to the changing size and location of the cyst.
View Article and Find Full Text PDFKorean J Spine
March 2016
Department of Neurosurgery, Acıbadem University Faculty of Medicine, Istanbul, Turkey.
A 32-year-old man presented with gradually increasing bilateral buttock pain. He had intermittent claudication. Multiple, homogenously enhanced intradural extramedullary lesions at L2-L3 and L5-S1 levels were observed on magnetic resonance imaging.
View Article and Find Full Text PDFChilds Nerv Syst
July 2016
Department of Pediatric Neurosurgery, Necker-Enfants Malades Hospital, Assistance Publique Hopitaux de Paris, Paris V University, 149 rue de Sèvres, 75015, Paris, France.
Purpose: Spinal lipoma of the filum terminale (LFT) is a congenital lumbosacral anomaly that can cause tethered cord syndrome. Purposes of this study are to clarify preoperative characteristics of LFT, to elucidate surgical effects, and to discuss the rationale of prophylactic surgery for LFT.
Methods: Medical data of 174 children (2008-2014) who underwent section of LFT were prospectively recorded for prevalence of symptoms, skin stigmas, and associated malformations, motivator of diagnosis, conus level, and surgical outcome.
Eur Spine J
May 2016
Department of Neurological Surgery, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, Tokyo, 113-8603, Japan.
Purpose: Symptoms of cauda equina syndrome due to ependymoma in the conus medullaris or filum terminale develop slowly. However, hemorrhagic change inside spinal tumors can induce acute neurologic decline. Here, we report a case of posttraumatic hemorrhage inside a filum terminale myxopapillary ependymoma presenting as acute neurologic decline, which had a positive prognosis after surgical resection.
View Article and Find Full Text PDFWe present a rare extramedullary ependymoma with diffuse spinal metastatic disease, and review the previous reports of extramedullary spinal ependymomas. Ependymomas are the most common intramedullary spinal cord tumor in adults. These tumors rarely present as extramedullary masses.
View Article and Find Full Text PDFPract Neurol
February 2016
Department of Radiology, University of Chicago Medical Center, Chicago, Illinois, USA.
Cauda equina syndrome refers to dysfunction of the cauda equina, the collection of ventral and dorsal lumbar, sacral and coccygeal nerve roots that surround the filum terminale. This most commonly occurs as a result of compression by a herniated lumbosacral disc. However, the syndrome may also complicate metastatic cancer or a primary neoplasm within or infiltrating the spinal canal.
View Article and Find Full Text PDFAsian J Neurosurg
September 2015
Department of Neurosurgery, Tashkent Pediatric Medical Institute, Tashkent, Uzbekistan.
A 9-year-old boy admitted to the neurosurgical hospital complaining of headache, vomiting, abdominal pain, and weakness in the arms and legs, urinary retention. Previously, the patient had a treatment of pediatricians. He was examined, magnetic resonance imaging revealed the tumor of the conus medullaris and cauda equina.
View Article and Find Full Text PDFNo Shinkei Geka
September 2015
Department of Neurosurgery, Otaru General Hospital.
Leptomeningeal metastasis is a rare entity and its diagnosis is often difficult. Moreover, evidence-based therapeutic strategies have not yet been established. A 52-year-old woman presented with high fever and was diagnosed with bacterial meningitis at first examination;although her fever was alleviated, she experienced motor weakness in both of her lower extremities.
View Article and Find Full Text PDFNeurosurg Focus
August 2015
Department of Neurosurgery, Christliches Krankenhaus, Quakenbrück, Germany.
OBJECT Ependymomas of the filum terminale provide specific surgical challenges due to their often enormous size, contact with nerve roots of the cauda equina and conus, and potential for subarachnoid dissemination. This study presents treatment results for these tumors over a 30-year period. METHODS Among 1447 patients with tumors of the spinal canal treated between 1980 and 2014, 618 patients presented with extramedullary tumors.
View Article and Find Full Text PDFJ Neurosurg Sci
December 2017
Division of Neurosurgery, Department of Surgery, American University of Beirut Medical Center, Beirut, Lebanon -
Migrating intra-spinal lesions are quite rare, and are most of the reported cases are schwannomas. Several theories have been proposed to explain the changing location of an intra-spinal tumor. We present a very rare case of migrating lumbar intra-spinal intra-dural lesion at the conus level, the pathology of which was an ependymoma, and review the possible etiologies of such a unique occurrence in view of the reported literature.
View Article and Find Full Text PDFJ Neurosurg Sci
December 2016
Department of Neurosurgery, Arad Hospital, Tehran, Iran -
Background: Myxopapillary ependymoma (MPE) is a rare variant of ependymoma usually occurring in the conus medullaris or the filum terminale. It is usually a single encapsulated lesion. The aim of this study was to describe patients with primary multifocal MPE of the filum terminale.
View Article and Find Full Text PDFJ Craniovertebr Junction Spine
January 2014
Department of Neurosurgery, King Edward Memorial Hospital, Seth Gordhandas Sunderdas Medical College, Parel, Mumbai, Maharashtra, India.
Context: Spinal paragangliomas are rare neuroendocrine tumors of the extra-adrenal paraganglionic system.
Aims: This study describes the clinicopathological features of eight cases of spinal paraganglioma and highlights the significance of important morphological features and immunohistochemistry in the diagnosis of paraganglioma at this unusual site.
Material And Methods: All the cases of primary spinal paragangliomas diagnosed during the last six years (2008-2013) in the Department of Pathology at our hospital were reviewed.
J Neurosurg Spine
September 2014
Department of Neurosurgery, Louisiana State University Health Sciences Center-Shreveport, Shreveport, Louisiana.
The authors report the case of a spinal intradural schwannoma presenting with intracranial subarachnoid hemorrhage (SAH). Cerebral angiography did not show any intracranial lesion; however, MRI revealed two separate tumors in the lower segment of the spinal cord. The proximal lesion arising from the conus medullaris was well circumscribed and homogeneously enhanced, whereas the tumor in the cauda equina revealed hemorrhagic signals on MRI.
View Article and Find Full Text PDFJ Neurosurg Pediatr
July 2014
Department of Neurosurgery, Brain Research Institute, University of Niigata, Japan.
Unlabelled: OBJECT.: Sacrococcygeal dimples in the gluteal fold, also known as coccygeal pits, are observed in 2%-4% of newborns. Sacrococcygeal dimples are not generally considered to be associated with a significant risk of intraspinal anomalies and therefore are not thought to require further radiographic evaluation.
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