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To investigate the incidence of cervical spine deformity and instability after posterior cervical spinal cord tumor (CSCT) resection without fusion or fixation in adults and examine relevant risk factors by reviewing and summarizing previously reported studies.We selected peer reviewed articles published between January 1990 and December 2020 from the MEDLINE and Cochrane Library databases using relevant key words. Articles in which the authors mainly described spinal cord tumor resection through posterior surgery without fusion or fixation in adults were selected for analysis. Patient's data including age, sex, extensive number of laminectomy levels, laminectomy at C2, C3, or C7, multilevel facetectomy, facet destruction, preoperative cervical kyphosis, and preoperative motor deficit were documented. Comparable factors were assessed using the odds ratio (OR) and weighted mean difference (WMD) of 95% confidence intervals (CI).Among 133 articles identified, 18 met selection criteria. Overall incidence of deformity and instability after CSCT surgery was 0%-41.7% and 0%-20.5%, respectively. Younger age (WMD, -5.5; 95% CI, -10.52 ∼ -0.49; P = 0.03), C2 laminectomy (OR, 5.33; 95% CI, 2.39 ∼ 11.91; P 0.0001), more laminectomy level (WMD, 2.77; 95% CI, 1.78 ∼ 3.76; P 0.00001) were identified as risk factors for deformity and instability after CSCT surgery.Patients undergoing CSCT resection should receive careful follow-up for postoperative spinal deformity and instability. Younger age, C2 laminectomy, and more laminectomy level were significantly associated with occurrence of deformity and instability after CSCT surgery. Upfront spinal fixation at the time of resection should be considered in selected patients.

Background/Objective Atlantoaxial fusion procedures may be difficult in situations such as high-riding vertebral artery, a narrow C2 pedicle, and the presence of ponticulus posticus–arcuate foramen. With respect to vertebral artery (VA) anomalies, persistent first intersegmental artery, extracranial origin of the posterior inferior cerebellar artery at the C1–C2 level, and fenestration of the VA are all major risk factors for VA injury in C1–C2 fusion surgeries. Methods To safeguard the VA, we designed the unilateral fusion procedure (all screws lie in the ipsilateral side, either the right side or left side): a unilateral transarticular screw combined with an ipsilateral-side C1 posterior arch screw and a C2 laminar screw (LS), with both C1–C2 screws inserted from opposite side, although the trajectory will be on the same side. In addition to atlantoaxial stabilization with screws and rod, autograft bony fusion was performed on the same side as modified Brook's procedure and augmented with sublaminar tapping. Results We present a series of 3 cases operated for odontoid fracture with associated high risk for fusion on one side alone. The fact that the chance of VA injury is high in transarticular screw, in lateral mass screw, less in pars screw, and pedicle screw is well known. Alternate screw placement to avoid VA injury would be a posterior arch screw for C1 and laminar screw for C2, which was adopted in our technique. Conclusions We combined a unilateral transarticular screw and modified Brook's procedure with sublaminar tapping for additional augmentation of fusion. We would like to highlight this C1 posterior arch screw as an alternative procedure for atlantoaxial fusion.

Diffuse idiopathic skeletal hyperostosis (DISH) is a well-recognized disease characterized by calcifications and ossifications of the entheses mainly in the spine. Patients with DISH are prone to sustaining spinal injuries even after minor trauma because of the long-lever arm mechanism induced by any type of force acting on the rigid yet brittle spine. The number of cases of trauma in DISH-affected spines is predicted to increase during the coming decades because of an increase in DISH-related comorbidities. Generally, posterior fixation with spinal instrumentation spanning three levels above and below the injured site is regarded as a standard treatment for hyperextension fractures of the thoracolumbar spine in patients with DISH. However, no consensus has been reached regarding whether additional anterior fixation is needed for hyperextension injuries with remarkable vertebral body wedge. We experienced one case of hyperextension injury at the thoracic level in patient with DISH. A remarkable remodeling phenomenon in the fractured vertebral body was intraoperatively noticed, which was pathologically confirmed. This is the first report to have confirmed pathologically new bone formation in the anterior column wedge despite the fact that only 1 month had passed since the first injury. Although whether additional anterior fixation is needed for hyperextension injuries with remarkable vertebral body wedge is controversial, this report supports that posterior fixation alone might be an adequate treatment.

Background Sacral schwannomas are rare tumors arising from nerve sheath Schwann cells. They are classified into 3 types: first type schwannoma arising from the sacrum, second type schwannoma eroding the sacrum, and third type schwannoma extending extensively, involving anterior, posterior, and retroperitoneal space. Among these type 2 sacral tumors, according to Klimo's classification, an eroding sacrum extending all over posteriorly, anteriorly, and laterally is still rarer. Only 38 cases have been reported in literature reviews. Only 6 cases of giant tumors of >10 cm in any 1 dimension have been reported. Case Description We present such a giant sacral schwannoma, with invasiveness eroding the sacrum; compressing the ureters, aortic bifurcation, bladder, and bowel; and presenting as lower abdominal pain, hydronephrosis, dysuria, and constipation. This is the first case reported in the literature that has described a large retroperitoneal tumor compressing retroperitoneal structures—aortic bifurcation vascular compression and ureter compression causing hydronephrosis. Conclusions Though complete resection, which caused various severe postoperative complications in the reported cases, is the best option, a less morbid procedure would be appropriate; hence we underwent subtotal excision of the tumor, with complete recovery of our patient's symptoms without neurologic deficit.

Background Formation of a dural arteriovenous fistula (DAVF) after lumbar spine decompression in the lumbar spine has been reported as a late complication, but is extremely rare in the cervical spine. Case Description A 57-year-old man who underwent a C5-6, C6-7 anterior fusion 5 years previously for cervical myelopathy at another hospital presented with progressive gait disturbance and thermal hypoalgesia on the right side of the body. Magnetic resonance imaging showed flow voids in the spinal cord dorsally at the C4-7 level, which had not been detected before the initial operation. Digital subtraction angiography showed a fistulous connection at the C7 level between the perimedullary vein and a segmental artery from the right vertebral artery, which was diagnosed as a DAVF. Surgical interruption of the intradural draining vein with multilevel posterior cervical decompression was performed, and his symptoms improved. Conclusions To the best of our knowledge, this is the first report of a DAVF developing after multilevel anterior cervical discectomy and fusion. All the published cases of secondary DAVF, especially after spinal surgery, are reviewed.

Background Ventral lesions of upper thoracic spinal cord due to degenerative diseases are rare and often have poor operative outcomes. Anterior decompression of the lesion is difficult because of the local anatomy. This retrospective study aimed to evaluate reproducible anatomic measurements for selecting the best surgical approach for anterior decompression of ventral lesions of upper thoracic spinal cord. Methods Cases of anterior decompression of ventral lesions of upper thoracic spinal cord due to degenerative diseases at our institution from 2004 to 2015 were assessed. Several lines were drawn on magnetic resonance imaging and computed tomography scans of midsagittal sections of the upper thoracic spine to evaluate the most optimal approach for treating upper thoracic lesions. A line from the suprasternal notch to the vertebral body (suprasternal notch to vertebral body [SV] line) was accepted as baseline. Results The caudal edge of the lesion was above the SV line in 10 cases, each of which was treated via an anterior approach without sternotomy. The caudal edge was below the SV line in 7 cases, 5 of which underwent surgery with the sternum-splitting or transthoracic approach. The other 2 lesions were approached via an obliquely deviated route without sternotomy. The SV line sometimes changed with patients' posture alterations. Conclusions The SV line, a useful landmark for upper thoracic lesions, is not sufficiently reliable because it changes according to the patient's posture. By leaning in the direction of the surgical microscope, more caudal upper thoracic lesions can be reached than when using the SV line as a surgical landmark.

Background Spinal epidural hematoma (SEH) is a potentially devastating problem that requires rapid diagnosis and surgical intervention. A chronic course is rarely seen following SEH, and the clinical characteristics are quite different from acute cases. The epidemiology, clinical history, and radiologic findings of chronic SEH (CSEH) are not well understood, although the detection rate has increased with the widespread use of magnetic resonance imaging. The purpose of this article was to report 4 cases of surgically confirmed CSEH and clarify the radiologic features and clinical scenarios by reviewing all published cases of CSEH. Case Description All 4 patients presented with gradually worsening radicular pain in the lower extremities. Patients’ mean age was 69.5 years (range, 55–85 years). Magnetic resonance imaging revealed an epidural mass in the lower lumbar spine that was heterogeneously enhanced after gadolinium administration. The rim of the mass was low intensity on T2*-weighted images. Local erosions of the adjacent cortical bone were seen with computed tomography in all cases. All patients’ postoperative courses were satisfactory with complete disappearance of radicular symptoms. Conclusions CSEH is a rare disease, and it is difficult to diagnose preoperatively on the basis of diagnostic imaging. The incidence of a low-intensity rim on T2*-weighted images and bone erosions on computed tomography may help differentiate rare CSEH from other lumbar degenerative diseases and epidural space-occupying masses.

Background Bone metastases from endometrial cancer are rare. To our knowledge, only 2 cases of solitary vertebral metastases from endometrial cancer presenting with osseous and/or neurologic symptoms before the diagnosis of the primary endometrial cancer have been reported; however, in both cases, the metastases were thoracic. Thus, cervical vertebral metastases are extremely rare. Case Description We describe the case of a 55-year-old woman who presented with right C6 radicular and neck pain. Neurologic imaging showed destruction of the C6 vertebral body by an extradural mass with kyphotic changes in the cervical spine. Fluorodeoxyglucose positron emission tomography showed increased uptake in the enlarged body of the uterus as well as the C6 vertebral body. Additional pelvic magnetic resonance images and endometrial biopsy confirmed endometrial cancer. The patient underwent excision of the cervical tumor with anterior reconstruction and posterior fixation followed 1 month later by semiradical hysterectomy and bilateral salpingo-oophorectomy with pelvic and para-aortic lymph node dissection. The cervical and endometrial histopathologic findings were similar, and the final diagnosis made was cervical metastatic adenocarcinoma originating from an endometrial cancer. Conclusions We describe an extremely rare case of a precocious solitary cervical metastasis from an endometrial cancer presenting as cervical radicular pain. In our review of published reports, we found that solitary spinal metastases are significantly associated with longer overall survival than are multiple lesions. Resection of the spinal lesion with rigid spinal reconstruction followed by radical hysterectomy may be beneficial in such patients.

The prevalence of fragility sacral fractures has been increasing with the rise in the number of osteoporotic patients and the development of diagnostic imaging. Sacral fracture can cause injury to the fifth lumbar (L5) nerve, although the incidence is low. The therapeutic strategy for sacral fracture with neurological injury has not yet been established, and the surgical strategy for fragility sacral fracture is more controversial. We describe a new therapeutic method using endoscopic surgery for L5 nerve root involvement caused by far-lateral lumbar disc herniation triggered by a fragility sacral fracture. A 55-year-old woman presented with right buttock and right lower limb pain without signs of trauma. Neurological examination revealed paresis of the right lower limb and hypoesthesia in the region innervated by the right L5 nerve root. Neuroimaging demonstrated a U-shaped sacral fracture, including the sacral ala, and right L5 extra-foraminal stenosis. The L5 nerve root was located near the vertical fracture, and compressed by far-lateral L5/S1 disc herniation. Full-endoscopic spine surgery (FESS) was performed to partially remove the right S1 superior articular process and to resect the degenerated disc material. L5 radiculopathy improved partially after the surgery. We suggest that FESS is an effective and safe therapeutic method for fragility sacral fractures associated with far-lateral lumbar disc herniation.

Surgical management of thoracic ossification of the posterior longitudinal ligament (OPLL) remains challenging because of the fragility of the thoracic spinal cord. Posterior approach with long instrumentation has been predominantly performed. However, this procedure includes the risk of neurologic deterioration caused by the progression of OPLL during long-term follow-up and the need for long instrumentation to achieve dekyphosis, even for so-called beaked-type OPLL between 1 vertebra. The present Video shows the microsurgical removal of OPLL in the middle thoracic level without spinal fusion, including the operative tips. The surgical techniques were demonstrated in detail handling patients with single OPLL. The patient is a 54-year-old woman with T5-6 OPLL. She presented with gradually worsening myelopathy and underwent the operation via the transthoracic anterolateral approach. Although intraoperative cerebrospinal fluid leakage occurred, it was successfully treated with fibrin glue sealing and spinal drainage. The modified Japanese Orthopaedic Association score improved from 5.5 preoperatively to 8.0 postoperatively. Postoperative deterioration of the thoracic kyphotic angle has not been noticed during the follow-up period of 149.7 months. Anterior decompression is the logical and ideal procedure to treat thoracic myelopathy caused by OPLL; however, this procedure is technically demanding. Microsurgery via the transthoracic anterolateral approach enables direct visualization of the thoracic ventral ossified lesion. Relatively narrow and little resection of the vertebral body under the presently demonstrated microsurgical procedures might negate the need for bone grafting or spinal instrumentation. The patient gave informed consent for surgery and video recording (Video 1).

Background Context Hemorrhage that results from spinal dural arteriovenous fistula (Type I arteriovenous malformation [AVM]) is uncommon. There are some reports of subarachnoid hemorrhage and subdural hematoma caused by Type I spinal AVM, but there are few reported cases of hematomyelia caused by spinal dural arteriovenous fistula. Purpose To describe an interesting patient who had hematomyelia caused by a dural arteriovenous fistula (Type I spinal AVM). Study design A case report. Methods We present a case of a 51-year-old man who presented acute onset epigastric pain, paraplegia, and sensory loss below his nipples. Magnetic resonance imaging and selective spinal angiogram demonstrated hematomyelia, subarachnoid hemorrhage, and spinal arteriovenous fistula fed by the right Th7 intercostal artery. By laminotomy of Th6–8, the varix-like draining vein and intramedurally hematoma were partially removed and the arterial supply was interrupted by coagulation of the right Th7 segmental artery. Results One month after surgery, he regained movement against gravity at the left ankle and toe but no functionally significant improvement. Conclusions It must be kept in mind that spinal dural arteriovenous fistulas (Type I spinal AVM) has possibility of hematomyelia origin, despite the fact that it is extremely rare.

BACKGROUND Subarachnoid hemorrhage (SAH) with a spinal origin is a rare clinical entity. The most common source of SAH is an arteriovenous malformation. Only six cases of spinal hemangioblastomas causing SAH have been reported. CASE DESCRIPTION This 48-year-old man had experienced severe headache 12 years earlier, which was diagnosed as SAH by computed tomography (CT) scan and lumbar puncture. However, cerebral angiography could not detect either aneurysm or arteriovenous malformation. Thereafter, he spent an uneventful life until he was incidentally diagnosed with a cervical tumor on magnetic resonance imaging (MRI) study for Meniere's disease. The tumor was situated at the cervicomedullary junction, and fed by the left vertebral artery. Histologic findings of the tumor showed features typical of hemangioblastoma. CONCLUSIONS We describe a case of cervical spinal extramedullary hemangioblastoma with a past history of SAH. In our case, the SAH of 12 years ago perhaps occurred from the cervicomedullary junction hemangioblastoma. Since the etiology of SAH could not be detected at the first angiography, not only follow-up reangiography, but also MRI of the spinal cord and spinal angiography could have played an important role.