ABSTRACT
PURPOSE: The topic of osseous variations of the craniocervical junction is a complex morphological and embryological chapter of human anatomy, with a possible impact on neurogical and vascular functionality in this morphological variable region. MATERIAL & METHODS: An until now undescribed anatomical variation of the exoccipital part of the occipital bone has been observed after maceration at the outer skull base of a West-European 68-year-old male body donor. RESULTS: On both sites of the foramen magnum accessory osseous processes were observed that arise from the jugular process and point towards the lateral margin of the foramen magnum. On the left site this process forms a full arc that bridges the condylar fossa completely. CONCLUSION: The observed osseous bridge over the condylar fossa has not been reported on before and can be explained by the partial persistence of a primordial vertebra between atlas and occipital bone: the Proatlas. The resulting accessory structure may affect due to its topographic conditions the V3-Segment of the vertebral artery and its accompanying nerves, and thus, play a role in diagnosis and therapy of vascular and/or neurological symptoms of head and neck.
Subject(s)
Anatomic Variation , Foramen Magnum , Occipital Bone , Skull Base , Humans , Male , Aged , Occipital Bone/abnormalities , Occipital Bone/anatomy & histology , Skull Base/anatomy & histology , Skull Base/diagnostic imaging , Foramen Magnum/anatomy & histology , Foramen Magnum/abnormalities , CadaverABSTRACT
Klippel-Feil syndrome (KFS) is characterized by the congenital fusion of the cervical vertebrae and is sometimes accompanied by anomalies in the craniocervical junction. In basilar invagination (BI), which is a dislocation of the dens in an upper direction, compression of the brainstem and cervical cord results in neurological defects and surgery is required. A 16-year-old boy diagnosed with KFS and severe BI presented with spastic tetraplegia, opisthotonus and dyspnea. CT scans showed basilar impression, occipitalization of C1 and fusion of C2/C3. MRI showed ventral compression of the medullocervical junction. Posterior occipitocervical reduction and fusion along with decompression were performed. Paralysis gradually improved postoperatively over 3 weeks. However, severe spasticity and opisthotonus persisted and intrathecal baclofen (ITB) therapy was initiated. Following this, opisthotonus disappeared and spasticity of the extremities improved. Rehabilitation therapy continued by controlling the dose of ITB. Five years after the surgery, self-propelled wheelchair driving was achieved and activities of daily life improved. The treatment strategy for patients with BI and congenital anomalies remains controversial. Posterior reduction and internal fixation using instrumentation were effective techniques in this case. Spasticity control achieved through a combination of surgery and ITB treatment enabled the amelioration of therapeutic efficacy of rehabilitation and the improvement of ADL.
Subject(s)
Baclofen , Cervical Vertebrae , Klippel-Feil Syndrome , Humans , Baclofen/therapeutic use , Baclofen/administration & dosage , Male , Klippel-Feil Syndrome/complications , Adolescent , Cervical Vertebrae/abnormalities , Cervical Vertebrae/surgery , Spinal Fusion/methods , Injections, Spinal/methods , Muscle Relaxants, Central/therapeutic use , Muscle Relaxants, Central/administration & dosage , Occipital Bone/abnormalities , Occipital Bone/surgery , Treatment Outcome , Decompression, Surgical/methodsABSTRACT
OBJECTIVE: Congenital anomalies of the atlanto-occipital articulation may be present in patients with Chiari malformation type I (CM-I). However, it is unclear how these anomalies affect the biomechanical stability of the craniovertebral junction (CVJ) and whether they are associated with an increased incidence of occipitocervical fusion (OCF) following posterior fossa decompression (PFD). The objective of this study was to determine the prevalence of condylar hypoplasia and atlas anomalies in children with CM-I and syringomyelia. The authors also investigated the predictive contribution of these anomalies to the occurrence of OCF following PFD (PFD+OCF). METHODS: The authors analyzed the prevalence of condylar hypoplasia and atlas arch anomalies for patients in the Park-Reeves Syringomyelia Research Consortium database who underwent PFD+OCF. Condylar hypoplasia was defined by an atlanto-occipital joint axis angle (AOJAA) ≥ 130°. Atlas assimilation and arch anomalies were identified on presurgical radiographic imaging. This PFD+OCF cohort was compared with a control cohort of patients who underwent PFD alone. The control group was matched to the PFD+OCF cohort according to age, sex, and duration of symptoms at a 2:1 ratio. RESULTS: Clinical features and radiographic atlanto-occipital joint parameters were compared between 19 patients in the PFD+OCF cohort and 38 patients in the PFD-only cohort. Demographic data were not significantly different between cohorts (p > 0.05). The mean AOJAA was significantly higher in the PFD+OCF group than in the PFD group (144° ± 12° vs 127° ± 6°, p < 0.0001). In the PFD+OCF group, atlas assimilation and atlas arch anomalies were identified in 10 (53%) and 5 (26%) patients, respectively. These anomalies were absent (n = 0) in the PFD group (p < 0.001). Multivariate regression analysis identified the following 3 CVJ radiographic variables that were predictive of OCF occurrence after PFD: AOJAA ≥ 130° (p = 0.01), clivoaxial angle < 125° (p = 0.02), and occipital condyle-C2 sagittal vertical alignment (C-C2SVA) ≥ 5 mm (p = 0.01). A predictive model based on these 3 factors accurately predicted OCF following PFD (C-statistic 0.95). CONCLUSIONS: The authors' results indicate that the occipital condyle-atlas joint complex might affect the biomechanical integrity of the CVJ in children with CM-I and syringomyelia. They describe the role of the AOJAA metric as an independent predictive factor for occurrence of OCF following PFD. Preoperative identification of these skeletal abnormalities may be used to guide surgical planning and treatment of patients with complex CM-I and coexistent osseous pathology.
Subject(s)
Arnold-Chiari Malformation , Atlanto-Occipital Joint , Cervical Atlas , Occipital Bone , Spinal Fusion , Syringomyelia , Humans , Arnold-Chiari Malformation/surgery , Arnold-Chiari Malformation/diagnostic imaging , Syringomyelia/surgery , Syringomyelia/diagnostic imaging , Female , Male , Cervical Atlas/abnormalities , Cervical Atlas/surgery , Cervical Atlas/diagnostic imaging , Child , Occipital Bone/surgery , Occipital Bone/diagnostic imaging , Occipital Bone/abnormalities , Spinal Fusion/methods , Adolescent , Atlanto-Occipital Joint/diagnostic imaging , Atlanto-Occipital Joint/surgery , Atlanto-Occipital Joint/abnormalities , Treatment Outcome , Child, Preschool , Decompression, Surgical/methods , Retrospective Studies , Cervical Vertebrae/surgery , Cervical Vertebrae/abnormalities , Cervical Vertebrae/diagnostic imagingABSTRACT
This report describes the clinical, computed tomography, and magnetic resonance imaging findings for a Jacob sheep lamb diagnosed with meningoencephalocele and supernumerary ectopic limb. Key clinical message: This case demonstrates the utility of tomographic imaging in diagnosing congenital malformations in sheep and can be used to assess the extent of the lesion. This may help to determine any viable treatment, or, as in the case presented here, determine that the extent of the lesion precludes surgical intervention.
Méningoencéphalocèle et membre ectopique surnuméraire provenant de l'os occipital chez un agneau Jacob. Ce rapport décrit les résultats cliniques, de tomodensitométrie et d'imagerie par résonance magnétique d'un agneau de Jacob chez qui on a diagnostiqué une méningoencéphalocèle et un membre ectopique surnuméraire.Message clinique clé :Ce cas démontre l'utilité de l'imagerie tomographique dans le diagnostic des malformations congénitales chez le mouton et peut être utilisée pour évaluer l'étendue de la lésion. Cela peut aider à déterminer tout traitement viable ou, comme dans le cas présenté ici, à déterminer que l'étendue de la lésion exclut une intervention chirurgicale.(Traduit par Dr Serge Messier).
Subject(s)
Meningocele , Sheep Diseases , Animals , Sheep , Encephalocele/diagnostic imaging , Encephalocele/veterinary , Meningocele/diagnosis , Meningocele/surgery , Meningocele/veterinary , Occipital Bone/abnormalities , Occipital Bone/pathology , Extremities , Tomography, X-Ray Computed/veterinary , Magnetic Resonance Imaging/veterinary , Sheep Diseases/diagnosisABSTRACT
AIM: To determine a quantitative relationship between the postoperative clivus slope (CS) and the change in the Patient-Reported Japanese Orthopaedic Association (PRO-JOA) scores following reduction surgery of the basilar invagination (BI). MATERIAL AND METHODS: A single center retrospective study was conducted. Patients who met the inclusion and exclusion criteria at our hospital during the period from August 2015 to August 2020 were identified. The CS was introduced. Radiographic parameters including the CS were measured to assess realignment preoperatively and postoperatively. The PRO-JOA score was recorded to reveal the clinical outcome. The PRO-JOA score and the radiographic parameters that included the CS were compared between postoperative BI patients. RESULTS: Ninety-four patients with BI were included in the study. The CS (0.96, 0.93-1.00) was inversely correlated with the PROJOA score. The CS was negatively associated with the ΔPRO-JOA score in the crude model, while no significant associations in the fully adjusted model, although in the case of the latter, a slight trend was found (p for trend < < 0.05). In the non-linear model, the CS was negatively associated with the ΔPRO-JOA score in patients diagnosed with BI, unless the CS exceeded 63.4°. CONCLUSION: A reduction in the CS affects the postoperative PRO-JOA score of BI patients. This relationship can be employed as a quantitative reference in determining preoperative design with respect to the intraoperative correction needed to reduce craniovertebral junction deformity in BI.
Subject(s)
Cervical Vertebrae , Cranial Fossa, Posterior , Humans , Cervical Vertebrae/diagnostic imaging , Cervical Vertebrae/surgery , Decompression, Surgical/methods , East Asian People , Patient Reported Outcome Measures , Retrospective Studies , Treatment Outcome , Cranial Fossa, Posterior/diagnostic imaging , Occipital Bone/abnormalities , Occipital Bone/diagnostic imaging , Occipital Bone/surgery , Craniofacial Abnormalities/complicationsABSTRACT
To identify skull-base growth patterns in Crouzon syndrome, we hypothesized premature minor suture fusion restricts occipital bone development, secondarily limiting foramen magnum expansion.Skull-base suture closure degree and cephalometric measurements were retrospectively studied using preoperative computed tomography (CT) scans and multiple linear regression analysis.Evaluation of multi-institutional CT images and 3D reconstructions from Wake Forest's Craniofacial Imaging Database (WFCID).Sixty preoperative patients with Crouzon syndrome under 12 years-old were selected from WFCID. The control group included 60 age- and sex-matched patients without craniosynostosis or prior craniofacial surgery.None.2D and 3D cephalometric measurements.3D volumetric evaluation of the basioccipital, exo-occipital, and supraoccipital bones revealed decreased growth in Crouzon syndrome, attributed solely to premature minor suture fusion. Spheno-occipital (ß = -398.75; P < .05) and petrous-occipital (ß = -727.5; P < .001) suture fusion reduced growth of the basioccipital bone; lambdoid suture (ß = -14â 723.1; P < .001) and occipitomastoid synchondrosis (ß = -16â 419.3; P < .001) fusion reduced growth of the supraoccipital bone; and petrous-occipital suture (ß = -673.3; P < .001), anterior intraoccipital synchondrosis (ß = -368.47; P < .05), and posterior intraoccipital synchondrosis (ß = -6261.42; P < .01) fusion reduced growth of the exo-occipital bone. Foramen magnum morphology is restricted in Crouzon syndrome but not directly caused by early suture fusion.Premature minor suture fusion restricts the volume of developing occipital bones providing a plausible mechanism for observed foramen magnum anomalies.
Subject(s)
Craniofacial Dysostosis , Craniosynostoses , Humans , Child , Foramen Magnum/diagnostic imaging , Foramen Magnum/surgery , Retrospective Studies , Craniofacial Dysostosis/diagnostic imaging , Craniofacial Dysostosis/surgery , Occipital Bone/diagnostic imaging , Occipital Bone/surgery , Occipital Bone/abnormalities , Cranial Sutures/diagnostic imaging , Craniosynostoses/diagnostic imaging , Craniosynostoses/surgery , SuturesABSTRACT
Morphological changes in the child skull due to mechanical and metabolic stimulation and synostosis of the suture are well known. On the other hand, few studies have focused on clinical conditions relevant for adult skull deformity. We retrospectively reviewed computed tomography (CT) findings obtained from 365 cases that were treated for head injuries, moyamoya disease, cervical internal carotid artery stenosis, and mental diseases, and investigated the morphological changes in the skull associated with these diseases. The findings from head injuries were used not only for control subjects, but also for the analysis of generational changes in skull shape based on birth year. Head shape had a brachiocephalic tendency with occipital flattening in people born from the 1950s onwards. Cases of moyamoya disease, cervical internal carotid artery stenosis, and mental diseases showed significantly thicker frontal and occipital bone than those of control subjects. The skull thickening was especially noticeable in the frontal bone in moyamoya disease. Plagiocephaly was significantly frequent in moyamoya disease. These uncommon skull shapes are useful CT findings in screening subjects for early evidence of mental diseases and intracranial ischemic diseases with arterial stenosis.
Subject(s)
Carotid Stenosis/pathology , Craniocerebral Trauma/pathology , Mental Disorders/pathology , Moyamoya Disease/pathology , Skull/abnormalities , Aged , Female , Frontal Bone/abnormalities , Frontal Bone/pathology , Humans , Male , Middle Aged , Occipital Bone/abnormalities , Occipital Bone/pathology , Retrospective Studies , Skull/pathology , Tomography, X-Ray ComputedABSTRACT
Atlas occipitalization (AO) is a spinal anomaly, characterized by the fusion of the first cervical vertebra and occipital bone, with a complex etiology that can arise from congenital and environmental causes. AO has been reported in three regions of pre-Hispanic Peru in skeletal remains with artificial cranial modification (ACM), which involves the use of compression devices to permanently alter cranial shape and may have affected the fusion of the atlas and occipital bone. The aims of this study were to gain insights into AO's etiology by testing correlations between AO and ACM presence/type and geographic region as well as to characterize morphological variation associated with AO. We investigated the geographic distribution of AO and its potential relationship to ACM in a large sample of human crania from eight coastal and highland regions of pre-Hispanic Peru, held at the Smithsonian's National Museum of Natural History (n = 608, 1300-1500 CE). Eleven cases of AO were observed in three coastal regions-including two previously unreported regions-at an overall frequency of 1.8%. The frequency of AO did not differ significantly between crania with and without ACM, in general or by type, suggesting that ACM is not an etiological factor that influences AO in this sample. AO was observed at a significantly higher rate in the southern coastal region of Arequipa than in any other region. Genetic, dietary, and epidemiological conditions are evaluated as factors possibly shaping the geographic distribution of AO along the central and southern coasts of Peru.
Subject(s)
Atlanto-Occipital Joint/abnormalities , Indians, South American/statistics & numerical data , Musculoskeletal Abnormalities/epidemiology , Occipital Bone/abnormalities , Archaeology , Cervical Atlas/abnormalities , Humans , PeruABSTRACT
BACKGROUND: Patients with Klippel-Feil syndrome may present with neurologic complaints such as neck pain, radiculopathy and gait instability. Here we describe surgical management of a patient with congenital fusion of the occipital-cervical region and also block circumferential fusion of dens to T3 with spinal cord compression. This report is the first of its kind with such extensive fusion. CASE DESCRIPTION: Our patient was a 56 year-old female, who presented with neck pain and tingling in all extremities. On exam, she had a short neck, prominent jaw with extremely limited range of motion in neck and features of myelopathy. CT showed fusion of the dens to T3 vertebrae. Patient underwent sub-occipital craniectomy, C1 laminectomy and Occiput to T5 posterior fixation and fusion with neurologic improvement. CONCLUSION: This is the first reported case of Klippel-Feil syndrome with fusion of all cervical vertebrae down to T3. We recommend surgery for advanced cases of myelopathy or radiculopathy due to stenosis and spinal instability.
Subject(s)
Cervical Vertebrae/diagnostic imaging , Klippel-Feil Syndrome/diagnostic imaging , Spinal Stenosis/diagnostic imaging , Thoracic Vertebrae/diagnostic imaging , Atlanto-Occipital Joint/diagnostic imaging , Atlanto-Occipital Joint/surgery , Cervical Vertebrae/abnormalities , Cervical Vertebrae/surgery , Craniotomy , Decompression, Surgical , Female , Humans , Joint Instability/diagnostic imaging , Joint Instability/surgery , Klippel-Feil Syndrome/complications , Klippel-Feil Syndrome/physiopathology , Klippel-Feil Syndrome/surgery , Laminectomy , Magnetic Resonance Imaging , Middle Aged , Neurosurgical Procedures , Occipital Bone/abnormalities , Occipital Bone/diagnostic imaging , Occipital Bone/surgery , Odontoid Process/abnormalities , Odontoid Process/diagnostic imaging , Odontoid Process/surgery , Spinal Fusion , Spinal Stenosis/etiology , Spinal Stenosis/physiopathology , Spinal Stenosis/surgery , Thoracic Vertebrae/abnormalities , Thoracic Vertebrae/surgery , Tomography, X-Ray ComputedABSTRACT
AIMS: To review and present the current knowledge of incidence, signs and symptoms, diagnosis and treatment of the occipital encephalocele. BACKGROUND: Encephalocele (E) is a defect of the neural tube that refers to congenital malformations featured by skull defect and dura with extracranial spread of intracranial structures. Occipital encephalocele (OE) are the most common form of this congenital disorder and are manifested as a swelling of different sizes over the occipital bone in the midline. Proper diagnosis and treatment is highly important in the management of this congenital malformation of brain. OBJECTIVE: To review and present the current knowledge of incidence, signs and symptoms, diagnosis and treatment of the occipital encephalocele. METHODS: We conducted a search of case reports or case-series of patients by the use of electronic databases: Pub Med, Medline, Index Medicus, Scorpus. The key words were: encephalocele, occipital encephalocele, neural tube defect, congenital malformation. The search was updated to December 31, 2018. Papers published in English were the only source of information. RESULTS: Occipital encephalocelle are more frequent in females than in males. The incidence is between 1 in 3000 to 1 in 10,000 live births; approximately 90% of them involve the midline. Magnetic resonance imaging is the method of choice in diagnosis and surgery is the best option for the treatment of OE. Overall morbidity and mortality is still high in spite of advenced surgical management, but have been significantly improved in recent years thanks to sophisticated highresolution imaging, adequate and proper surgical treatment and decent post-operative care. CONCLUSION: Occipital encephalocele is the most common form of encephalocele. The diagnosis is mostly based by the use of neuroimaging techniques. Operation is the best option for treatment. Overall morbidity and mortality is still high, but have been significantly improved in recent years thanks to sophisticated high-resolution imaging, adequate and proper surgical treatment and decent post-operative care.
Subject(s)
Encephalocele , Occipital Bone/abnormalities , Encephalocele/diagnostic imaging , Encephalocele/epidemiology , Encephalocele/etiology , Encephalocele/surgery , Humans , Incidence , Neuroimaging/methods , Neurosurgical Procedures/methods , Occipital Bone/diagnostic imaging , PrognosisABSTRACT
Objective: To examine the effect of posterior reduction in atlantoaxial dislocation (AAD) associated with basilar invagination(BI) using Xuanwu occipital-cervical fusion system in single stage. Methods: Thirty-seven AAD accompanied with BI cases treated at Department of Neurosurgery, Xuanwu Hospital, Capital Medical Universiy and the Second Hospital of Hebei Medical University were retrospective analyzed. There were 15 males and 22 females with age of (42.3±12.3)years (range: 18-69 yars). All the cases had congenital osseous abnormalities, such as assimilation of atlas and abnormal cervical fusion. Anterior tissue was released through posterior route followed by cage implantation into facet joint and occipital-cervical fixation with cantilever technique. The clinical results were evaluated using Japanese Orthopedic Association scale(JOA) and the main radiological measurements including anterior atlantodental interval (ADI),the distance of odontoid tip above Chamberlain line,clivus-canal angle (CCA) and the length of syrinx were collected.The preoperative and postoperative JOA score and radiological measurements were compared by paired t-test. Results: The mean JOA score of the patients increased from 10.5 to 14.4 at the one-year follow-up(t=14.3,P=0.00).Complete reduction of AAD and BI was achieved in 34 patients.The mean clivus-canal angle improved from 118.0 degrees preoperative to 143.7 degrees postoperative(t=6.2,P=0.00). Shrinkage of the syrinx was observed 1 week after surgery in 24 patients, and 6 months in 31 patients. Twenty-eight patients achieved bone fusion 6 months after surgery. All the patients achieved bone fusion 12 months after surgery. One-side vertebral artery occlusion was diagnosed in 1 case postoperatively for transient dizziness, and relieved in 2 weeks. Two patients developed moderate neck pain after surgery, and relieved in 1 month. No implant failure, spacer subsidence or infection was observed. Conclusions: The treatment of AAD associated with BI using Xuanwu occipital-cervical fusion system from posterior approach in single stage is effective and safe. Cage implantation intraarticularly and fixation with cantilever technique achieve complete reduction in most cases.
Subject(s)
Atlanto-Axial Joint/surgery , Decompression, Surgical/methods , Joint Dislocations/surgery , Platybasia/surgery , Spinal Fusion/methods , Adolescent , Adult , Aged , Cervical Vertebrae/abnormalities , Cervical Vertebrae/surgery , Decompression, Surgical/instrumentation , Female , Humans , Joint Dislocations/complications , Male , Middle Aged , Occipital Bone/abnormalities , Occipital Bone/surgery , Retrospective Studies , Spinal Fusion/instrumentation , Young AdultABSTRACT
BACKGROUND: Scaphocephaly is usually defined as the deformation of the skull resulting from the premature fusion of the sagittal suture. It is the most common type of craniosynostosis, and can be easily recognized on simple clinical examination. Its pathophysiology is easy to understand and to confirm on neuroradiological examination. In contrast, surgical indications are still somewhat controversial, the dispute mainly concerning therapeutic versus esthetic objectives. In recent years, however, several studies have challenged these basic and relatively simplistic interpretations of the pathophysiology of the condition. MATERIALS AND METHODS: To assess the heterogeneity of scaphocephaly, we reviewed cases of scaphocephaly operated on at the Hôpital Femme-Mère-Enfant, Lyon University Hospital, France during a 10-year period (2008-2017) and performed a review of the literature on scaphocephaly and sagittal suture closure. RESULTS: During the 10-year period, 401 children were operated on for a scaphocephaly at the Hôpital Femme Mère Enfant, Lyon University Hospital. Mean age at surgery was 1.14 years, for a median 0.7 years (range, 4 months to 8. 5 years). Several subtypes could be distinguished according to morphology, intracranial findings on imaging, patient age, and etiology associated to the sagittal synostosis. Two main surgical techniques were used to correct the malformation, depending on patient age, type of deformation and the surgeon's preference: cranial vault remodeling with occipital pole widening, with the patient in a prone position, and parietal enlargement with or without forehead remodeling, in dorsal decubitus. CONCLUSIONS: The complexity and heterogeneous nature of sagittal synostoses depend on different pathogenic mechanisms leading to and interfering with the skull abnormalities: abnormalities of CSF dynamics, possibly associated with systemic alterations, accounting for the varied postoperative morphological and functional course, in terms of cognitive impairment and late complications (notably intra-cranial pressure elevation). However, the real impact of such heterogeneous clinical presentations on surgical indications and surgical results remains to be elucidated.
Subject(s)
Cranial Sutures/pathology , Cranial Sutures/surgery , Craniosynostoses/pathology , Craniosynostoses/surgery , Age Factors , Child , Child, Preschool , Cranial Sutures/diagnostic imaging , Craniosynostoses/diagnostic imaging , Disease Progression , Female , Forehead/abnormalities , Forehead/surgery , Humans , Infant , Intracranial Hypertension , Male , Occipital Bone/abnormalities , Occipital Bone/surgery , Patient Positioning , Skull/abnormalities , Skull/surgeryABSTRACT
BACKGROUND: Patients with basilar invagination and atlas occipitalization usually present abnormal anatomy of the vertebral arteries (VAs) at the craniovertebral junction (CVJ). OBJECTIVE: To describe and further classify different types of VA variations at the CVJ with 3D visualization technology. METHODS: One hundred twenty patients with basilar invagination and atlas occipitalization who had undergone 3-dimensional computed tomographic angiography (3D-CTA) were retrospectively studied. Imaging data were processed via the separating, fusing, opacifying, and false-coloring-volume rendering technique. Abnormal anatomy of the VA at the CVJ was categorized and related anatomic parameters were measured. RESULTS: Seven different types were classified. Type I, VAs enter the cranium after leaving VA groove on the posterior arch of atlas (26.7% of 240 sides); Type II, VAs enter an extraosseous canal created in the assimilated atlas lateral mass-occipital condyle complex before reaching the cranium (53.3%); Type III, VA courses above the axis facet or curves below the atlas lateral mass then enter the cranium (11.7%); Type IV, VAs enter the spinal canal under the axis lamina (1.3%); Type V, high-riding VA (31.3%); Type VI, fenestrated VA (2.9%); Type VII, absent VA (4.2%). Distance from the canal of Type II VA to the posterior facet surface of atlas lateral mass (5.51 ± 2.17 mm) means a 3.5-mm screw can be safely inserted usually. Shorter distance from the midline (13.50 ± 4.35) illustrates potential Type III VA injury during exposure. Decreased height and width of axis isthmus in Type V indicate increased VA injury risks. CONCLUSION: Seven types of VA variations were described, together with valuable information helpful to minimize VA injury risk intraoperatively.
Subject(s)
Central Nervous System Vascular Malformations/diagnostic imaging , Cervical Atlas/abnormalities , Occipital Bone/abnormalities , Platybasia/diagnostic imaging , Vertebral Artery/diagnostic imaging , Adolescent , Adult , Central Nervous System Vascular Malformations/classification , Central Nervous System Vascular Malformations/complications , Cerebral Angiography , Child , Computed Tomography Angiography , Female , Humans , Imaging, Three-Dimensional , Male , Middle Aged , Musculoskeletal Abnormalities/complications , Retrospective Studies , Vertebral Artery/abnormalities , Young AdultABSTRACT
Occipital spur is an abnormal bony outgrowth of the external occipital protuberance (EOP). We describe an interesting and previously unreported case of fracture of an occipital spur following trauma. Our 20-year-old male patient was treated in the emergency department (ED) and discharged home without complication. Neurosurgical consultation was obtained but is not requisite for these injuries. Greater awareness of this unique presentation may help to expedite future emergency department treatment.
Subject(s)
Occipital Bone/diagnostic imaging , Skull Fractures/diagnostic imaging , Anatomic Variation , Humans , Lacerations/therapy , Male , Occipital Bone/abnormalities , Occipital Bone/injuries , Scalp , Skull Fractures/therapy , Suture Techniques , Therapeutic Irrigation , Tomography, X-Ray Computed , Young AdultABSTRACT
An adult male skeleton was submitted to the Department of Anatomy at the University of Belgrade for evaluation. It was believed to represent the remains of a second to third century Christian saint from the Lesje Monastery in central Serbia. Examination of the remains revealed an old crush fracture of a thoracic vertebra and an unusual, probably congenital, malformation of the atlanto-occipital joint with deformation of the left occipital condyle and resultant narrowing of the foramen magnum. Although the occipital malformations were most likely congenital, they may still have caused, or contributed to, death by compression of the underlying upper cervical spinal cord.
Subject(s)
Atlanto-Occipital Joint/abnormalities , Crush Injuries/pathology , Saints/history , Thoracic Vertebrae/injuries , Adult , Foramen Magnum/abnormalities , Foramen Magnum/diagnostic imaging , Forensic Anthropology , History, Ancient , Humans , Male , Occipital Bone/abnormalities , Occipital Bone/diagnostic imaging , Religion and Medicine , Serbia , Skull/anatomy & histology , Thoracic Vertebrae/pathology , Tomography, X-Ray ComputedSubject(s)
Encephalocele/diagnostic imaging , Fetal Diseases/diagnostic imaging , Occipital Bone/abnormalities , Prenatal Diagnosis/methods , Amniocentesis/methods , Cytogenetics/methods , Encephalocele/congenital , Encephalocele/surgery , Female , Fetal Diseases/genetics , Homeodomain Proteins/genetics , Humans , Karyotype , Magnetic Resonance Imaging/methods , Occipital Bone/diagnostic imaging , Pregnancy , Treatment Outcome , Young AdultABSTRACT
Torticollis could be the only symptom and sign of craniovertebral junction (CVJ) abnormality. It could be difficult to identify CVJ abnormality as a cause of torticollis due to their rarity, especially for the subjects with torticollis caused by nontraumatic CVJ abnormalities. There has been no report to focus on nontraumatic CVJ abnormalities as a cause of torticollis. The objective of this study was to report 27 patients of torticollis caused by nontraumatic CVJ abnormalities, with the aim of helping clinicians to identify nontraumatic CVJ abnormalities as a cause of torticollis. This is a retrospective cohort study including 27 subjects who had torticollis caused by nontraumatic CVJ abnormalities. The CVJ was examined in terms of atlanto-occipital angle, atlanto-axial angle, and lateral and anterior atlanto-dens intervals for the evaluation of occipital condylar hypoplasia, rotation of atlanto-axial joint, and lateral and anterior shift of the dens, respectively. Abnormalities of the lower cervical or thoracic spine were also evaluated. Occipital condylar hypoplasia, rotation of atlanto-axial joint, and lateral shift of the dens were the most common CVJ abnormalities. The 18.5% of the subjects had concurrent anomalies of lower cervical or thoracic vertebrae along with CVJ abnormalities. Each subject had 2.22â±â1.10 types of CVJ abnormalities on average. In conclusion, comprehensive evaluation of CVJ abnormalities is recommended for differential diagnosis of subjects with unexplained torticollis. Once CVJ abnormalities are identified, concurrent abnormalities of other vertebrae need to be evaluated.
Subject(s)
Atlanto-Axial Joint/abnormalities , Atlanto-Occipital Joint/abnormalities , Occipital Bone/abnormalities , Odontoid Process/abnormalities , Torticollis/etiology , Adolescent , Adult , Child , Child, Preschool , Female , Humans , Infant , Male , Musculoskeletal Abnormalities/complications , Retrospective Studies , Thoracic Vertebrae/abnormalities , Young AdultABSTRACT
The craniovertebral junction (CVJ) is the bony transition between the cranium and cervical spine. It is a biomechanically complex articulation comprising the occipital condyles (Oc) the atlas (C1) and axis (C2). Pathologies affecting the CVJ in children are myriad with clinical features resulting from biomechanical instability, deformity, or neuraxial compression. Establishing the natural history and clinical burden of a condition is challenging in infants and young children, often complicated by co-existing neuromuscular and cognitive impairment. This makes investigation and treatment planning difficult. Each disease entity has a predilection for a particular biomechanical abnormality. Investigation using dynamic imaging is most appropriate in instability, computed tomography examination in abnormalities of deformity and magnetic resonance imaging examination in neuraxial compression. Treatment comprises reduction and immobilisation of instability, re-alignment of deformity, or decompression of the neuraxis. We present a review of disease entities affecting the CVJ in children categorised according to a simple mechanistic approach to aid investigation and treatment planning.