Primary craniovertebral anomalies and the hindbrain herniation syndrome (Chiari): Data base analysis

被引:130
作者
Menezes, AH
机构
[1] Division of Neurosurgery, University of Iowa Hospitals/Clinics, Iowa City, IA 52242
关键词
Chiari malformation; craniovertebral junction anomaly;
D O I
10.1159/000120969
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
This prospective study analyzes 100 patients with Chiari malformation and primary craniovertebral junction (CVJ) anomalies (3-66 years). Neurodiagnostic investigations employed tomography, gas myelography, CT and CT myelography, and MRI. Factors considered were reducibility, mode of encroachment, cerebrospinal fluid (CSF) dynamics and syringohydromyelia. Sixty-six patients with irreducible pathology underwent ventral or ventrolateral decompression and dorsal stabilization. Dorsal occipitocervical fixation was performed in reducible lesions that also required dorsal decompression (n = 34). Proatlas remnants were identified in 8 and atlas assimilation in 92 patients. Paramesial invagination was present in 20, syringohydromeylia in 46, and vertebral segmentation defects in 66 others. Completely reducible abnormalities were identified in 16 of 20 patients aged 2-14 years, and partially reducible abnormalities in 4 of 16 patients aged 14-20 years, 8 of 48 patients aged 20-40 years and 6 of 16 patients aged 40-60 years. The critical sagittal canal diameter at the foramen magnum was 19 mm. Twenty-two patients had previous posterior decompression and 27 had previous syrinx to subarachnoid shunt with delayed deterioration. Improvement occurred in all after ventral or ventrolateral decompression with resolution of the syringohydromyelia and normalization of CSF flow. We conclude that: (1) hindbrain herniation syndrome is frequently seen with fourth occipital sclerotome abnormalities; (2) Chiari malformation with craniovertebral abnormalities become symptomatic with a canal diameter of <19 mm: (3) abnormal ventral bony pathology is reducible in children with atlas assimilation and later becomes irreducible invagination, therefore early operation with fusion is recommended; (4) ventral decompression relieves brain stem, cerebellar symptoms and syringohydromyelia; (5) CSF studies with cine MRI shows reversal of craniospinal CSF dissociation after ventral CVJ decompression and; (6) craniovertebral anomalies associated with Chiari malformations must be addressed early and appropriately. (C) 1996 Karger AG, Basel
引用
收藏
页码:260 / 269
页数:10
相关论文
共 43 条
[1]
AREY LB, 1965, DEVELOPMENTAL ANATOM, P404
[2]
QUANTITATIVE CINE-MODE MAGNETIC-RESONANCE-IMAGING OF CHIARI-I MALFORMATIONS - AN ANALYSIS OF CEREBROSPINAL-FLUID DYNAMICS [J].
ARMONDA, RA ;
CITRIN, CM ;
FOLEY, KT ;
ELLENBOGEN, RG .
NEUROSURGERY, 1994, 35 (02) :214-223
[3]
Early development of the cervical vertebral and the base of the occipital bone in man [J].
Bardeen, CR .
AMERICAN JOURNAL OF ANATOMY, 1908, 8 (01) :181-186
[4]
Bystrow A, 1931, Z ANAT ENTW GESCH, V95, P210
[5]
CONSIDERATIONS IN THE DIAGNOSIS AND TREATMENT OF SYRINGOMYELIA AND THE CHIARI MALFORMATION [J].
CAHAN, LD ;
BENTSON, JR .
JOURNAL OF NEUROSURGERY, 1982, 57 (01) :24-31
[6]
DEBARROS MC, 1968, J NEUROL NEUROSUR PS, V31, P596
[7]
DEBEER GR, 1937, DEV VERTEBRATE SKULL, P356
[8]
CRANIOVERTEBRAL JUNCTION MALFORMATIONS - CLINICORADIOLOGICAL FINDINGS, LONG-TERM RESULTS, AND SURGICAL INDICATIONS IN 63 CASES [J].
DILORENZO, N ;
FORTUNA, A ;
GUIDETTI, B .
JOURNAL OF NEUROSURGERY, 1982, 57 (05) :603-608
[9]
FAWCETT E, 1910, J ANAT PHYSL, V44, P303
[10]
GAN GULY D. N., 1964, ANAT ANZ, V114, P433