Evidence map›Paper›PMID 41477392›Full record

ArticleCureus2025

Surgical Management of Cervical Myelopathy Due to Congenital Synostosis at the Craniovertebral Junction: Vertebral Artery Anomalies and Full-Endoscopic Retropharyngeal Odontoidectomy in a Case Series of Five Patients.

Hiroshi Kageyama, Yukoh Ohara, Hirohiko Arimoto, Toru Maeda, Koichi Sairyo

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Hiroshi KageyamaOrthopedics, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, JPN.
Yukoh OharaNeurosurgery, Juntendo University, Tokyo, JPN.
Hirohiko ArimotoNeurological Surgery, Shin-Kuki General Hospital, Kuki, JPN.
Toru MaedaOrthopedics, Anan Medical Center, Anan, JPN.
Koichi SairyoOrthopedics, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, JPN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital synostosis at the craniovertebral junction (CVJ), including C1 assimilation and C2-C3 fusion, can lead to cervical myelopathy due to adjacent segment stenosis or instability. These anomalies are rare and frequently associated with vertebral artery (VA) variations, which complicate surgical planning and instrumentation. This case report describes five patients who developed cervical myelopathy associated with congenital CVJ synostosis and were surgically treated at our institution between 2019 and 2023. Preoperative imaging, including computed tomography (CT), magnetic resonance imaging (MRI), and CT angiography, was used to evaluate bony anomalies and VA morphology. Posterior decompression and fusion were performed under navigation guidance, with screw selection tailored to the individual anatomy. Among the five patients (mean age, 74.8 years), three had C1 assimilation, four had C2-C3 fusion, and two had both. VA anomalies, such as high-riding VA and unilateral hypoplasia, were present in all patients with C2-C3 fusion, requiring modified screw trajectories to prevent vascular injury. Three patients underwent full-endoscopic retropharyngeal odontoidectomy for persistent ventral compression after posterior fixation. All patients showed postoperative neurological improvement, and no VA injury or screw malposition occurred. Imaging confirmed sufficient decompression and appropriate fixation. Congenital CVJ synostosis with associated VA anomalies presents unique surgical challenges. Preoperative vascular imaging and intraoperative navigation are essential for safe fixation, and full-endoscopic retropharyngeal odontoidectomy offers a minimally invasive and effective option for anterior decompression in selected cases.

Indexed as

craniovertebral junctiondecompressionendoscopemyelopathysynostosisvertebral artery

Identifiers

PMID41477392
PMCPMC12751519

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