Ossification of the cervical anterior longitudinal ligament contributing to dysphagia - Case report

Citation
Ne. Epstein et R. Hollingsworth, Ossification of the cervical anterior longitudinal ligament contributing to dysphagia - Case report, J NEUROSURG, 90(4), 1999, pp. 261-263
Citations number
12
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
JOURNAL OF NEUROSURGERY
ISSN journal
00223085 → ACNP
Volume
90
Issue
4
Year of publication
1999
Supplement
S
Pages
261 - 263
Database
ISI
SICI code
0022-3085(199904)90:4<261:OOTCAL>2.0.ZU;2-R
Abstract
The authors evaluated the clinical, radiological, and surgical management o f ossification of the anterior longitudinal ligament (OALL) that contribute d to dysphagia in a patient with simultaneous cervical ossification of the posterior longitudinal ligament (OPLL). A 57-year-old man presented with in creasing dysphagia and moderate myelopathy. Imaging studies, including esop hagoscopy, revealed marked esophageal compression due to GALL that extended between the C2-5 levels and significant C5-7 OPLL that compressed the dist al cervical spinal cord. The use of rongeurs and a high-speed drill facilit ated excision of the C2-5 GALL mass, and a routine anterior corpectomy with fusion was performed at the C5-7 level. Postoperatively, the patient's dys phagia and symptoms of myelopathy immediately resolved. The strut graft bec ame fully fused 3 months postoperatively, as demonstrated on dynamic x-ray films, and the patient has remained asymptomatic 4 months postoperatively. Patients with dysphagia and coexisting myelopathy benefit from simultaneous surgery for resection of GALL and OPLL masses.