Pediatric Chiari malformation type I: long‑term outcomes following small‑bone‑window posterior fossa decompression with autologous‑fascia duraplasty

  • Authors:
    • Hai Liu
    • Chenlong Yang
    • Jun Yang
    • Yulun Xu
  • View Affiliations

  • Published online on: September 27, 2017
  • Pages:5652-5658
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Chiari malformation type I (CM‑I) is a common hindbrain disorder that is associated with deformity and elongation of the cerebellar tonsils. Although CM‑I occurs in both pediatric and adult patients, its prevalence, clinical features and management in the pediatric population are not well defined. The current study evaluated a consecutive case series of 92 children (38 females and 54 males) who were diagnosed with congenital CM‑I. All patients underwent small‑bone‑window posterior fossa decompression with autologous‑fascia duraplasty. Clinical and radiological features were analyzed and long‑term follow‑up data were recorded. Risk factors associated with clinical outcomes were investigated using comprehensive statistical methods. Out of the 92 children, 11 (12.0%) were asymptomatic. Associated ventricular dilation was observed in 24 children (26.1%) and concomitant syringomyelia was observed in 72 children (78.3%). A total of 44 children (47.8%) showed scoliosis on plain films. Follow‑up data (mean duration, 88.6 months) were available for all patients. Syringomyelia was absent or markedly reduced in 56 patients (77.8%). Symptoms were alleviated in 66 patients, remained unchanged in 12 patients and progressed in 3 patients. Statistical analysis indicated that the cerebellar tonsillar descent (CTD) grade, basilar invagination and platybasia influenced the clinical outcome (P<0.05). In conclusion, early recognition and surgical treatment of CM‑I in pediatric patients can lead to good outcomes. The current results suggested that small‑bone‑window posterior fossa decompression with autologous‑fascia duraplasty was an effective safe treatment option with a low complication rate. High CTD grade, basilar invagination and platybasia were indicated to be predictors of poor clinical prognosis.


Chiari malformation (CM) is a hindbrain disorder that is associated with deformity and elongation of the cerebellar tonsils. It is specifically characterized by the descent of the cerebellar tonsils >5 mm below the foramen magnum into the spinal canal (1,2). CM can be divided into four types, among which CM type I (CM-I) is the most common. Although CM-I occurs in pediatric and adult patients, the prevalence of CM-I is not well defined (2). CM-I often becomes clinically apparent when the patient is aged 20–39. Thus, in the past, CM-I had been diagnosed primarily during adolescence or adulthood (2,3). With the advent of magnetic resonance imaging (MRI), however, the number of pediatric patients diagnosed with CM-I is increasing (4). Previous studies have described the clinical features of CM-I in pediatric populations (2,5,6).

CM-I is usually associated with ventricular dilation, syringomyelia and scoliosis, but the relevant pathogenesis is not clearly understood. Moreover, the incidence of these conditions co-presenting with CM-I has varied considerably in previous studies (710).

Management of CM-I and concomitant syringomyelia and scoliosis in children remains controversial. Some authors have recommended syringoperitoneal shunting for treating syringomyelia (11,12). The treatment of scoliosis consists of serial observation, bracing and/or corrective spinal surgery. It is yet to be established whether aggressive surgical treatment is necessary, and the ideal therapeutic option is undetermined (13). It is widely accepted, however, that posterior fossa decompression should be included in the treatment protocol for CM-I as it can lead to both clinical and radiological improvement (8,14,15). The use of specific surgical procedures and related issues, however, remain controversial; these include the use of craniectomy, the size of the bone window, whether the arachnoid should be opened and whether a cerebellar tonsil should be manipulated (14,15).

The current study evaluated a consecutive case series of 92 children who were diagnosed with CM-I. Their clinical manifestations, concomitant ventricular dilation, syringomyelia, basilar invagination, platybasia and scoliosis were analyzed. The study also evaluated the surgical outcomes of small-bone-window posterior fossa decompression (SPFD) with autologous-fascia duraplasty (AFD) in the treatment of pediatric CM-I.

Patients and methods

Patient recruitment

A search of medical records was conducted to identify pediatric patients (aged 0–18 years at their initial presentation to the neurosurgery clinic) with CM-I who had been operated on in the Department of Neurosurgery at Beijing Tiantan Hospital, Capital Medical University (Beijing, China). The cohort included 92 children (female:male ratio, 1.00:1.42; mean age ± standard deviation, 10.0±4.5) with congenital CM-I who were treated with SPFD + AFD between January 2001 and January 2015. CM-I was diagnosed according to the following criteria (1): i) Herniation of tonsils ≥5 mm was below the plane of the foramen magnum; or ii) tonsillar herniation of 3–5 mm accompanied by other CM-I features, such as syringomyelia. Exclusion criteria were as follows: i) Occipitocervical instability; ii) congenital spinal bifida; iii) diastematomyelia; iv) concurrent intraspinal tumors or myelitis; v) acquired CM-I as a complication of cerebrospinal fluid (CSF) diversion procedures or chronic CSF leakage; and vi) incomplete data. The study protocol was approved by the Institutional Review Board and Ethics Committee of Beijing Tiantan Hospital, Capital Medical University.

Clinical presentation

Subjective clinical symptoms and physical examinations were documented. Symptoms recorded included headache, foramen magnum nerve compression symptoms (occipitocervical headaches, neck or shoulder pain), sensory disturbance, motor dysfunction (weakness or muscle atrophy), lower cranial nerve dysfunction (dysphagia, hoarseness or coughing), cerebellar syndrome (truncal and appendicular ataxia) and scoliosis. Some patients also had bradycardia. Following the exclusion of endocrine dysfunction and organic heart disease by comprehensive evaluations, including laboratory, electrophysiological and radiological examinations, these symptoms were suspected to be associated with CM-I or with concomitant syringomyelia.


Preoperative plain radiographs and perioperative MRI scans of the cervical spine were available for all patients. The descending distance between the inferior pole of the cerebellar tonsil and the level of the foramen magnum was measured on sagittal T1-weighted images in a picture archiving and communication system workstation (OsiriX software; version 6.0; Pixmeo SARL, Bernex, Switzerland). The degree of cerebellar descent was classified into three groups according to the cerebellar tonsillar descent (CTD) grading system (16): Grade I, the tonsil descends over the foramen magnum but does not reach the C1 arch; Grade II, the tonsil descends to the C1 arch level; and Grade III, the tonsil descends below the C1 arch. The location of the syringomyelia was determined on sagittal MRI images, and its size was determined by measuring the longitudinal and transverse diameters.

The data for concomitant scoliosis were collected from standing posteroanterior radiographs (Fig. 1), and coronal curvature measurements were performed according to the Cobb method (17). Scoliosis was defined as a Cobb's angle of ≥10°. Curve severity was defined as follows: mild, 10–25°; moderate, 26–40°; severe, ≥41°. In cases of S-shaped scoliosis, the major curve was selected for analysis and the minor curves were considered compensatory.

Other associated abnormalities were also recorded, such as ventricular dilation, platybasia and basilar invagination. Ventricular dilation was defined by an Evans' index of >0.30 (18).

Surgical approach

Surgery was performed on all children with a combined strategy that included SPFD and AFD. After patients were positioned left-laterally, a posterior midline skin incision was made from 1 cm below the inion to the spinous process of C4. An autologous graft (2×2 cm) was resected from the fascia and reserved. The SPFD procedure, which included a small-bone-window suboccipital craniectomy (diameter, 2.0–2.5 cm) and C-1 laminectomy (1.5 cm), was performed. The thick constraining dural band found at the occipitocervical junction was resected. When the dura mater was opened, the surgeon aimed to keep the arachnoid intact. The dura mater was subsequently grafted with the autologous graft to enlarge the cisterna magna. Six children presented with progressive hydrocephalus and severe intracranial hypertension, and an emergency ventriculoperitoneal shunt was implanted in these cases (Fig. 2).


Follow-up data for all children were available in their records. The data had been obtained during individual office visits or telephone interviews, with a mean follow-up time of 88.6 months (standard deviation, 46.2; range, 10–166 months). Clinical outcomes were qualitatively categorized as follows: i) Improved, the patients experienced partial or complete relief of their chief complaints; or ii) not improved, no notable change in their chief complaints, or deterioration of their clinical status. Furthermore, the clinical outcomes were quantitatively evaluated according to the Chicago Chiari Outcome Scale (CCOS; Table I) (19).

Table I.

Chicago Chiari outcome scale.

Table I.

Chicago Chiari outcome scale.


PainWorseUnchanged and refractory to medicationImproved or controlled with medicationResolved
Non-painWorseUnchanged or improved but impairedImproved and unimpairedResolved
FunctionalityUnable to attendModerate impairment (<50% attendance)Mild impairment (>50% attendance)Fully functional
ComplicationPersistent complication, poorly controlledPersistent complication, well-controlledTransient complicationUncomplicated course
Statistical analysis

SPSS 22.0 software (IBM SPSS, Armonk, NY, USA) was used for statistical analyses. Chi-squared test, continuity correction test or Fisher's exact probability test were used to screen the potential risk factors, including age at onset, age at diagnosis, sex, duration of symptoms, CTD grades, concomitant syringomyelia, hydrocephalus, basilar invagination, platybasia and scoliosis. Logistic regression analysis was performed to identify the risk factors for clinical outcomes (binary-classification qualitative data). Furthermore, to verify the association between potential risk factors and clinical outcomes, CCOS scores (continuous variables) were compared using one-way analysis of variance (ANOVA) with a Bonferroni post hoc test test for multi-group comparisons and Mann-Whitney U test for two-group comparison. P≤0.05 was considered to indicate a statistically significant significance.


Patient population and clinical characteristics

Over the 14-year span of this study, 98 pediatric patients were diagnosed with CM-I and underwent SPFD + AFD. Six patients were lost to follow-up and excluded. This case series consisted of 38 females and 54 males, with a female:male ratio of 1.00:1.42. The average age at the time of surgery was 10.0±4.5 years (range, 1–18 years). In total, 11 (12.0%) children were asymptomatic. In the symptomatic group (n=81), the duration of symptoms preceding the initial diagnosis ranged from 2 weeks to 4 years (mean, 16.8 months). A total of 59 children presented with headache (72.8% of all symptomatic children), 17 with foramen magnum nerve compression symptoms (21.0%), 29 with sensory disturbance (35.8%), 36 with motor dysfunction (44.4%), 7 with lower cranial nerve dysfunction (8.6%) and 16 with cerebellar syndrome (19.8%). In addition, the results of electrocardiography, which is performed routinely upon admission, indicated that 4 patients had atrioventricular block (3 patients with second-degree and 1 patient with third-degree block), with no relevant underlying disease detected. None of the children complained of bowel or bladder dysfunction.

Preoperative MRI

The distance of tonsillar herniation ranged from 6.0 to 18.4 mm (mean, 11.2±3.2 mm). On the preoperative MRI, platybasia was observed in 5 children (5.4%) and basilar invagination in 12 children (13.0%). Associated ventricular dilation was observed in 24 children (26.1%). Concomitant syringomyelia was observed in 72 children (78.3%): Cervical syringomyelia (n=4; 5.6% of concomitant syringomyelia cases), cervicothoracic syringomyelia (n=67; 93.0%) and holocord syringomyelia (n=1; 1.4%).

Scoliosis evaluation

A total of 44 children (47.8%; 19 females and 25 males) showed scoliosis on plain films: 35 children had C-shaped thoracic scoliosis in a single curve; 8 children had S-shaped thoracic scoliosis with two adjacent curves; and 1 child had S-shaped thoracolumbar scoliosis. According to the severity classification, 26 children were diagnosed with mild scoliosis, 12 with moderate scoliosis and 6 with severe scoliosis. Further analysis indicated that all children with scoliosis had concomitant syringomyelia. In total, 36 (81.8%) of the children with scoliosis also had a unilateral sensory disturbance and/or motor disturbance or unilateral muscle atrophy. These data are summarized in Table II.

Table II.

Characteristics of coexisting scoliosis.

Table II.

Characteristics of coexisting scoliosis.

CharacteristicNumberPercentage (%)
Curve type
  C-shaped thoracic scoliosis3579.5
  S-shaped thoracic scoliosis  818.2
  S-shaped thoracolumbar scoliosis  12.3
Curve orientation
  Convex to the left2045.5
  Convex to the right2454.5
  Mild (10–25°)2659.1
  Moderate (26–40°)1227.3
  Severe (>41°)  613.6
Complications and follow-up

There were no deaths in this series. Central nervous system infection occurred postoperatively in four children. Antibiotics were prescribed and the infections were effectively treated. Suboccipital hydrops was noted in two children (Fig. 3). During the follow-up period, symptoms were alleviated in 66 patients (81.5% of all the symptomatic children), remained unchanged in 12 patients (14.8%) and progressed in 3 patients (3.7%). Preoperatively, 72 patients had concomitant syringomyelia. According to follow-up MRI scans, syringomyelia was absent or markedly reduced in 56 of these patients (77.8%; Fig. 4). Analysis of these results using Chi-squared tests indicated that CTD grades and the incidence of basilar invagination (Fig. 5) and platybasia were associated with clinical outcomes (P<0.05); the statistical data are summarized in Table III. Logistic regression analysis indicated that a high CTD grade [P=0.016; odds ratio (OR)=3.675; 95% confidence interval (CI), 1.138–8.527], basilar invagination (P=0.008; OR=3.489; 95% CI, 1.048–10.754) or platybasia (P=0.002; OR=3.981; 95% CI, 1.654–9.386) significantly increased the likelihood of poor clinical outcomes. A comparison of CCOS scores by ANOVA also indicated that CTD grade, and basilar invagination and platybasia by Mann-Whitney U tests are predictors of poor clinical prognosis (P<0.05; Table IV).

Table III.

Results of Chi-squared tests.

Table III.

Results of Chi-squared tests.

CharacteristicChi-square valueP-value
Age at onset (<10 vs. >10 years)0.3050.581
Age at diagnosis (<10 vs. >10 years)0.0070.932
Sex (male vs. female)0.2680.605
Duration (<16.8 vs. >16.8 months)1.5220.217
CTD (Grade I–III)14.2240.001
Syringomyelia (present vs. absent)0.683a0.408a
Hydrocephalus (present vs. absent)1.658a0.198a
Basilar invagination (present vs. absent)11.864a0.001a
Platybasia (present vs. absent)0.004b
Scoliosis (present vs. absent)1.8970.168

a Continuity correction.

b Fisher's exact probability. CTD, cerebellar tonsillar descent.

Table IV.

Results of statistical analyses.

Table IV.

Results of statistical analyses.

CTD (Grade I–III)Basilar invagination (present vs. absent)Platybasia (present vs. absent)

Clinical CCOS assessmentF valueP-valueZ valueP-valueZ valueP-value
Composite CCOS score3.5800.032−4.9270.000−3.6010.000
Pain subscore0.1390.871−6.2150.000−3.9960.000
Non-pain subscore3.4590.036−3.6290.000−3.4510.001
Functionality subscore3.9420.023−3.5780.000−4.1250.000
Complications subscore0.9840.378−1.1770.239−1.5730.116

[i] CTD, cerebellar tonsil descent; CCOS, Chicago Chiari outcome scale.


CM-I is a craniocervical junction disorder characterized by a cerebellar tonsil descending below the foramen magnum into the spinal canal. This was first described by Hans Chiari in 1891 (1). The incidence of CM-I has been reported to be 0.5–3.5% in the general population (20). A previous study reported a slight female predominance (female/male ratio 1.3:1.0) (20), although this is inconsistent with the findings in the current study (female/male ratio 1.00:1.52). CM-I is generally considered a congenital neurological condition, although in recent years its acquired form has been identified as a complication of CSF diversion procedures or chronic CSF leakage (21,22).

CM-I is thought to be a multifactorial condition, although the pathogenesis is still undetermined. A well-accepted hypothesis is that the hindbrain tissues are dislocated into the spinal canal because of an overcrowded posterior cranial fossa, due to underdevelopment of the mesodermal occipital somite (23). Previous morphometric results have supported this postulation. The posterior fossa volume in CM-I patients was reported to be smaller compared with the control group, although the difference was not statistically significant (23,24). In addition, some familial cases suggest a genetic component (25).

The incidence of syringomyelia in CM-I patients has ranged widely in previous reports, from 30 to 70% (20). The exact prevalence of syringomyelia in pediatric patients remains unclear. In the current study, a high syringomyelia occurrence rate (78.3%) was observed in CM-I patients. There are several hypotheses concerning the development of syringomyelia in the CM-I context, including the ‘water-hammer’ mechanism proposed by Gardner (26) and the ‘pressure dissociation’ mechanism proposed by Williams (27). However, most authors agree that partial obstruction in the foramen magnum area, which blocks the normal circulation of CSF, is the pacing factor in the development of syringomyelia (28).

Diagnosis of CM-I depends on MRI (29). For a long time, the diagnostic criteria have been under debate. Barkovich et al (30) proposed that 3 mm below the foramen magnum was the lowest extent of tonsillar descent in normal patients, and defined CM-I as >3 mm of tonsillar descent. Others have proposed that 5 mm of tonsillar ectopia should be adopted as the cutoff for diagnosing CM-I (2). In addition, Mikulis et al (31) reported that age affects the normal position of cerebellar tonsils and proposed age-based diagnostic criteria. These were as follows: In patients aged 0–9, the cutoff distance for tonsillar descent should be 6 mm; in patients aged 10–29, it should be 5 mm; in patients aged 30–79 years it should be 4 mm; and at >79 years of age, it should be 3 mm (31). Considering the fact that patients with lesser degrees of tonsillar ectopia (3–5 mm) may also develop classic neurological symptoms and syringomyelia that are amenable to neurosurgical intervention, the current study adopted the more flexible comprehensive diagnostic criteria proposed by Tubbs et al (1).

Patients with CM-I can be asymptomatic or can present with a variety of signs and symptoms ranging from headache to severe myelopathy and brain stem compression (29). With the increasing availability of diagnostic MRI, more asymptomatic patients are being identified (4). In the adult population, 15–30% of CM-I patients are asymptomatic (20). In the current study, 11 (12.0%) asymptomatic children were identified. Innate bias, however, is inevitable in an in-hospital cohort. Sleep apnea and feeding problems are reported to be more common in pediatric patients, although other clinical manifestations appear to be similar in different age groups (6). As previously reported, the most common presenting symptom of CM-I is headache (4), which is consistent with the current findings. In infants and children who are unable to communicate verbally, headaches may manifest as crying and irritability. Other common symptoms include non-radicular pain in the shoulder, back and extremities, motor and sensory disturbances, clumsiness, ataxia and lower cranial nerve dysfunction (29). In the current cohort, two patients with atrioventricular block were also identified.

There is no effective non-surgical strategy for treating patients with CM-I (12). Posterior fossa decompression, with or without dural opening, and with or without arachnoid opening or dissection, is most commonly used for the surgical treatment of CM-I and can change its clinical course (13,32). However, the size of the bone window required for posterior fossa decompression is still under debate (33,34). Furthermore, it has not yet been established whether a difference exists in the operative techniques used for pediatric and adult patients. Large-bone-window posterior fossa decompression effectively enlarges the posterior cranial fossa and therefore relieves symptoms (35). However, there may be a higher incidence of complications, such as CSF leak, pseudocysts, meningitis and hydrocephalus (35). Furthermore, excessive removal of the squamous part of the occipital bone could lead to downward and backward displacement of the cerebellum and brain stem, leading to long-term complications. According to a previous study, small-bone-window craniectomy is enough to achieve favorable clinical outcomes, and the incidence of complications is reduced (35). The procedure described in the aforementioned study relieves the compression of the occipitocervical bones and preserves enough bone to support the cerebellum and brain stem. In the current study, all patients underwent a small-bone-window approach, with which high rates of clinical (81.5%) and radiological (77.8%) improvement were achieved.

Whether it is necessary to open the arachnoid space is another focus of controversy. Some authors assert that CSF-related complications, such as CSF leak or meningitis, are directly associated with opening the arachnoid (36). A previous study has indicated that the incidence of CSF leaks is not higher in the arachnoid-opening group, provided that watertight duraplasty is performed (37). Furthermore, reconstruction of the cisterna magna and tonsillar manipulation could contribute to a better prognosis (37). It is the current authors’ opinion that arachnoid opening is unnecessary in most patients; SPFD and duraplasty without arachnoid incision is sufficient to relieve compression and alleviate clinical symptoms. It should be noted that the incidence of CSF-related complications was low in the pediatric cohort of the current study.

The prevalence of scoliosis in the general pediatric population is 2–4%, while in children with CM-I the prevalence of scoliosis is >4-fold increase (9,38). Progressive scoliosis is a relatively common manifestation of CM-I when there is coexistent syringomyelia (38). In the current study, the incidence of scoliosis was markedly higher (47.8%) in CM-I patients compared with the reported prevalence in the general pediatric population. Nokes et al (39) identified 3 patients with CM-I and scoliosis, but without syringomyelia. In the current cohort, all scoliotic children had coexistent syringomyelia. Considering the relatively mild severity of pediatric scoliosis, spinal orthopedic surgery was not recommended for the majority of these patients. It was considered that brace treatment could effectively reverse scoliotic progression. Eule et al (40) conducted a 20-year review of surgical and nonsurgical treatment in a pediatric cohort with CM-I associated with syringomyelia and scoliosis. It was found that early decompression of CM-I helped stabilize or alleviate the associated scoliosis, avoiding the requirement for orthopedic spinal surgery.

The current study had several limitations. Preoperatively, the scoliosis evaluations were based only on standing posteroanterior radiographs. The absence of side-bending radiographs limited a three-dimensional assessment. During the follow-up period, only MRI scans were performed. Plain radiography was not performed in all of the patients. Therefore, the present study did not track the progression of scoliosis. Furthermore, for ethical reasons, there were no control groups undergoing large-bone-window posterior fossa decompression or arachnoid opening in the current study.

In conclusion, early recognition and surgical treatment of pediatric CM-I leads to good outcomes in the majority of patients. SPFD with duraplasty was demonstrated to be an effective, safe treatment option with a low complication rate. High CTD grade, basilar invagination and platybasia were indicated to be predictors of poor clinical prognosis.



Tubbs RS, Lyerly MJ, Loukas M, Shoja MM and Oakes WJ: The pediatric Chiari I malformation: A review. Childs Nerv Syst. 23:1239–1250. 2007. View Article : Google Scholar : PubMed/NCBI


Aitken LA, Lindan CE, Sidney S, Gupta N, Barkovich AJ, Sorel M and Wu YW: Chiari type I malformation in a pediatric population. Pediatr Neurol. 40:449–454. 2009. View Article : Google Scholar : PubMed/NCBI


Dones J, De Jesús O, Colen CB, Toledo MM and Delgado M: Clinical outcomes in patients with Chiari I malformation: A review of 27 cases. Surg Neurol. 60:142–148. 2003. View Article : Google Scholar : PubMed/NCBI


Poretti A, Ashmawy R, Garzon-Muvdi T, Jallo GI, Huisman TA and Raybaud C: Chiari type 1 deformity in children: Pathogenetic, clinical, neuroimaging, and management aspects. Neuropediatrics. 47:293–307. 2016. View Article : Google Scholar : PubMed/NCBI


Albert GW, Menezes AH, Hansen DR, Greenlee JD and Weinstein SL: Chiari malformation Type I in children younger than age 6 years: Presentation and surgical outcome. J Neurosurg Pediatr. 5:554–561. 2010. View Article : Google Scholar : PubMed/NCBI


Amin R, Sayal P, Sayal A, Massicote C, Pham R, Al-Saleh S, Drake J and Narang I: The association between sleep-disordered breathing and magnetic resonance imaging findings in a pediatric cohort with Chiari 1 malformation. Can Respir J. 22:31–36. 2015. View Article : Google Scholar : PubMed/NCBI


Tubbs RS, Doyle S, Conklin M and Oakes WJ: Scoliosis in a child with Chiari I malformation and the absence of syringomyelia: Case report and a review of the literature. Childs Nerv Syst. 22:1351–1354. 2006. View Article : Google Scholar : PubMed/NCBI


Ono A, Suetsuna F, Ueyama K, Yokoyama T, Aburakawa S, Numasawa T, Wada K and Toh S: Surgical outcomes in adult patients with syringomyelia associated with Chiari malformation type I: The relationship between scoliosis and neurological findings. J Neurosurg Spine. 6:216–221. 2007. View Article : Google Scholar : PubMed/NCBI


Krieger MD, Falkinstein Y, Bowen IE, Tolo VT and McComb JG: Scoliosis and Chiari malformation type I in children. J Neurosurg Pediatr. 7:25–29. 2011. View Article : Google Scholar : PubMed/NCBI


Strahle J, Smith BW, Martinez M, Bapuraj JR, Muraszko KM, Garton HJ and Maher CO: The association between Chiari malformation type I, spinal syrinx, and scoliosis. J Neurosurg Pediatr. 15:607–611. 2015. View Article : Google Scholar : PubMed/NCBI


Isik N, Elmaci I, Isik N, Cerci SA, Basaran R, Gura M and Kalelioglu M: Long-term results and complications of the syringopleural shunting for treatment of syringomyelia: A clinical study. Br J Neurosurg. 27:91–99. 2013. View Article : Google Scholar : PubMed/NCBI


Morina D, Petridis AK, Fritzsche FS, Ntoulias G and Scholz M: Syringomyelia regression after shunting of a trapped fourth ventricle. Clin Pract. 3:e12013. View Article : Google Scholar : PubMed/NCBI


Whitson WJ, Lane JR, Bauer DF and Durham SR: A prospective natural history study of nonoperatively managed Chiari I malformation: Does follow-up MRI surveillance alter surgical decision making. J Neurosurg Pediatr. 16:159–166. 2015. View Article : Google Scholar : PubMed/NCBI


Guyotat J, Bret P, Jouanneau E, Ricci AC and Lapras C: Syringomyelia associated with type I Chiari malformation. A 21-year retrospective study on 75 cases treated by foramen magnum decompression with a special emphasis on the value of tonsils resection. Acta Neurochir (Wien). 140:745–754. 1998. View Article : Google Scholar : PubMed/NCBI


Beecher JS, Liu Y, Qi X and Bolognese PA: Minimally invasive subpial tonsillectomy for Chiari I decompression. Acta Neurochir (Wien). 158:1807–1811. 2016. View Article : Google Scholar : PubMed/NCBI


Yilmaz A, Kanat A, Musluman AM, Colak I, Terzi Y, Kayacı S and Aydin Y: When is duraplasty required in the surgical treatment of Chiari malformation type I based on tonsillar descending grading scale? World Neurosurg. 75:307–313. 2011. View Article : Google Scholar : PubMed/NCBI


Morrissy RT, Goldsmith GS, Hall EC, Kehl D and Cowie GH: Measurement of the Cobb angle on radiographs of patients who have scoliosis. Evaluation of intrinsic error. J Bone Joint Surg Am. 72:320–327. 1990. View Article : Google Scholar : PubMed/NCBI


Ambarki K, Israelsson H, Wåhlin A, Birgander R, Eklund A and Malm J: Brain ventricular size in healthy elderly: Comparison between Evans index and volume measurement. Neurosurgery. 67:94–99. 2010. View Article : Google Scholar : PubMed/NCBI


Yarbrough CK, Greenberg JK, Smyth MD, Leonard JR, Park TS and Limbrick DD Jr: External validation of the Chicago Chiari outcome scale. J Neurosurg Pediatr. 13:679–684. 2014. View Article : Google Scholar : PubMed/NCBI


Arnautovic A, Splavski B, Boop FA and Arnautovic KI: Pediatric and adult Chiari malformation Type I surgical series 1965–2013: A review of demographics, operative treatment, and outcomes. J Neurosurg Pediatr. 15:161–177. 2015. View Article : Google Scholar : PubMed/NCBI


Atkinson JL, Weinshenker BG, Miller GM, Piepgras DG and Mokri B: Acquired Chiari I malformation secondary to spontaneous spinal cerebrospinal fluid leakage and chronic intracranial hypotension syndrome in seven cases. J Neurosurg. 88:237–242. 1998. View Article : Google Scholar : PubMed/NCBI


Riffaud L, Moughty C, Henaux PL, Haegelen C and Morandi X: Acquired Chiari I malformation and syringomyelia after valveless lumboperitoneal shunt in infancy. Pediatr Neurosurg. 44:229–233. 2008. View Article : Google Scholar : PubMed/NCBI


Urbizu A, Poca MA, Vidal X, Rovira A, Sahuquillo J and Macaya A: MRI-based morphometric analysis of posterior cranial fossa in the diagnosis of chiari malformation type I. J Neuroimaging. 24:250–256. 2014. View Article : Google Scholar : PubMed/NCBI


Furtado SV, Reddy K and Hegde AS: Posterior fossa morphometry in symptomatic pediatric and adult Chiari I malformation. J Clin Neurosci. 16:1449–1454. 2009. View Article : Google Scholar : PubMed/NCBI


Shimojima K, Okamoto N, Tamasaki A, Sangu N, Shimada S and Yamamoto T: An association of 19p13.2 microdeletions with Malan syndrome and Chiari malformation. Am J Med Genet A. 167A:724–730. 2015. View Article : Google Scholar : PubMed/NCBI


Gardner WJ: Hydrodynamic mechanism of syringomyelia: Its relationship to myelocele. J Neurol Neurosurg Psychiatry. 28:247–259. 1965. View Article : Google Scholar : PubMed/NCBI


Williams B: On the pathogenesis of syringomyelia: A review. J R Soc Med. 73:798–806. 1980.PubMed/NCBI


Koyanagi I and Houkin K: Pathogenesis of syringomyelia associated with Chiari type 1 malformation: Review of evidences and proposal of a new hypothesis. Neurosurg Rev. 33:271–285. 2010. View Article : Google Scholar : PubMed/NCBI


McVige JW and Leonardo J: Neuroimaging and the clinical manifestations of Chiari malformation type I (CMI). Curr Pain Headache Rep. 19:182015. View Article : Google Scholar : PubMed/NCBI


Barkovich AJ, Wippold FJ, Sherman JL and Citrin CM: Significance of cerebellar tonsillar position on MR. AJNR Am J Neuroradiol. 7:795–799. 1986.PubMed/NCBI


Mikulis DJ, Diaz O, Egglin TK and Sanchez R: Variance of the position of the cerebellar tonsils with age: Preliminary report. Radiology. 183:725–728. 1992. View Article : Google Scholar : PubMed/NCBI


Chotai S and Medhkour A: Surgical outcomes after posterior fossa decompression with and without duraplasty in Chiari malformation-I. Clin Neurol Neurosurg. 125:182–188. 2014. View Article : Google Scholar : PubMed/NCBI


Menezes AH: Current opinions for treatment of symptomatic hindbrain herniation or Chiari type I malformation. World Neurosurg. 75:226–228. 2011. View Article : Google Scholar : PubMed/NCBI


Abd-El-Barr M and Groff MW: Less is more: Limiting the size of posterior fossa decompressions in Chiari I malformations. World Neurosurg. 81:706–707. 2014. View Article : Google Scholar : PubMed/NCBI


Bao C, Yang F, Liu L, Wang B, Li D, Gu Y, Zhang S and Chen L: Surgical treatment of Chiari I malformation complicated with syringomyelia. Exp Ther Med. 5:333–337. 2013. View Article : Google Scholar : PubMed/NCBI


Navarro R, Olavarria G, Seshadri R, Gonzales-Portillo G, McLone DG and Tomita T: Surgical results of posterior fossa decompression for patients with Chiari I malformation. Childs Nerv Syst. 20:349–356. 2004. View Article : Google Scholar : PubMed/NCBI


Alfieri A and Pinna G: Long-term results after posterior fossa decompression in syringomyelia with adult Chiari Type I malformation. J Neurosurg Spine. 17:381–387. 2012. View Article : Google Scholar : PubMed/NCBI


Godzik J, Dardas A, Kelly MP, Holekamp TF, Lenke LG, Smyth MD, Park TS, Leonard JR and Limbrick DD: Comparison of spinal deformity in children with Chiari I malformation with and without syringomyelia: Matched cohort study. Eur Spine J. 25:619–626. 2016. View Article : Google Scholar : PubMed/NCBI


Nokes SR, Murtagh FR, Jones JD III, Downing M, Arrington JA, Turetsky D and Silbiger ML: Childhood scoliosis: MR imaging. Radiology. 164:791–797. 1987. View Article : Google Scholar : PubMed/NCBI


Eule JM, Erickson MA, O'Brien MF and Handler M: Chiari I malformation associated with syringomyelia and scoliosis: A twenty-year review of surgical and nonsurgical treatment in a pediatric population. Spine (Phila Pa 1976). 27:1451–1455. 2002. View Article : Google Scholar : PubMed/NCBI

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December 2017
Volume 14 Issue 6

Print ISSN: 1792-0981
Online ISSN:1792-1015

2016 Impact Factor: 1.261
Ranked #50/128 Medicine Research and Experimental
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Liu, H., Yang, C., Yang, J., & Xu, Y. (2017). Pediatric Chiari malformation type I: long‑term outcomes following small‑bone‑window posterior fossa decompression with autologous‑fascia duraplasty. Experimental and Therapeutic Medicine, 14, 5652-5658.
Liu, H., Yang, C., Yang, J., Xu, Y."Pediatric Chiari malformation type I: long‑term outcomes following small‑bone‑window posterior fossa decompression with autologous‑fascia duraplasty". Experimental and Therapeutic Medicine 14.6 (2017): 5652-5658.
Liu, H., Yang, C., Yang, J., Xu, Y."Pediatric Chiari malformation type I: long‑term outcomes following small‑bone‑window posterior fossa decompression with autologous‑fascia duraplasty". Experimental and Therapeutic Medicine 14, no. 6 (2017): 5652-5658.