Myelopathy at the level of the atlas is rarely encountered by the practicing spine surgeon. Due to the region's unique anatomy, compression of the cord at this level is either caused by a large compressing lesion or an abnormally stenotic canal. We describe a rare instance of a congenitally stenotic canal due to a hypoplastic intact posterior arch of atlas, coexisting with an extremely rare ossified transverse ligament of the atlas. The coexistence of these two lesions has only been documented thrice before. We describe the clinical presentation, imaging findings, and favorable response to surgery.
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http://dx.doi.org/10.1155/2012/893284 | DOI Listing |
Cureus
December 2024
Department of Orthopaedic Surgery, The Jikei University School of Medicine, Tokyo, JPN.
Ossification of the ligamentum flavum (OLF) can lead to dural ossification, significantly increasing the risk of complications, including intraoperative nerve injury. The application of augmented reality (AR) and advanced digital technologies in spine surgery has the potential to reduce these risks. This case report highlights a perioperative nerve injury-free microsurgery using elastic image fusion technology, which integrates preoperative imaging with intraoperative computed tomography for a patient with severe stenotic OLF and dural ossification.
View Article and Find Full Text PDFCureus
November 2024
Radiology, University of Texas Medical Branch, Galveston, USA.
Based on the available literature, duplicated internal auditory canals (DIACs) represent an exceedingly rare temporal bone anomaly that can result in sensorineural hearing loss (SNHL) in the pediatric population. Often associated with a hypoplastic or aplastic cochlear nerve, DIAC poses limitations on treatment options, such as cochlear implants, for affected patients. Accurate diagnosis and optimal management necessitate a thorough assessment of inner ear structures and potential neural abnormalities with high-resolution computed tomography and magnetic resonance imaging of the temporal bones.
View Article and Find Full Text PDFBone Joint J
November 2024
Department of Orthopaedics and Traumatology, The University of Hong Kong, Hong Kong SAR, China.
Aims: Developmental cervical spinal stenosis (DcSS) is a well-known predisposing factor for degenerative cervical myelopathy (DCM) but there is a lack of consensus on its definition. This study aims to define DcSS based on MRI, and its multilevel characteristics, to assess the prevalence of DcSS in the general population, and to evaluate the presence of DcSS in the prediction of developing DCM.
Methods: This cross-sectional study analyzed MRI spine morphological parameters at C3 to C7 (including anteroposterior (AP) diameter of spinal canal, spinal cord, and vertebral body) from DCM patients (n = 95) and individuals recruited from the general population (n = 2,019).
Biomech Model Mechanobiol
October 2024
Department of Neurosurgery, Medical College of Wisconsin, Watertown Plank Road, Milwaukee, WI, 870153226, USA.
Spinal cord stress and strain contribute to degenerative cervical myelopathy (DCM), while cervical kyphosis is known to negatively impact surgical outcomes. In DCM, the relationship between spinal cord biomechanics, sagittal alignment, and cord compression is not well understood. Quantifying this relationship can guide surgical strategies.
View Article and Find Full Text PDFZhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi
April 2024
Department of Otorhinolaryngology, Zhengzhou University First Affiliated Hospital, Zhengzhou 450052, China.
To assess the clinical features and CT diagnostic characteristics of Branchio-Oto-Renal or Branchio-Oto Syndrome The temporal CT findings and clinical features observations of 13 patients with Branchio-Oto-Renal Syndrome (BORS) or Branchio-Oto Syndrome(BOS) confirmed by genetic testing were retrospectively analyzed. There were 8 males and 5 females, aged from 1 to 39 years, with a median age of 9 years, in which 3 pairs (6 cases) were parent-child relationship. All of 13 cases had hearing loss and preauricular fistula, 11 cases accompanied by 2nd branchial fistulas.
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