Skip to main content
Top
Published in: Child's Nervous System 10/2019

01-10-2019 | Scoliosis | Special Annual Issue

Clinical diagnosis—part I: what is really caused by Chiari I

Authors: Palma Ciaramitaro, Marilena Ferraris, Fulvio Massaro, Diego Garbossa

Published in: Child's Nervous System | Issue 10/2019

Login to get access

Abstract

Purpose

Chiari malformation is a group of congenital malformations involving the brainstem, cerebellum, and upper spinal cord, frequently identified in both young adults and in children. Chiari I malformation (CM1), classically defined as a caudal displacement of the cerebellar tonsils through the foramen magnum into the spinal cord, is the most common clinical type. A syringomyelia can be associated at the time of the diagnosis or appear secondarily and manifest with medullary symptoms. The aim of this paper is to update the knowledge on clinical manifestations specifically related to Chiari I malformation with or without syringomyelia in the pediatric population.

Methods

Current literature with focus on relevant clinical pediatric issues is reviewed and discussed, comparing with those related to adults; we include the results of a 10-year single-center experience on 600 CM1 patients.

Results and conclusions

Herniation of the cerebellar tonsils may lead to significant clinical symptoms, including neck and cervical pain, short-lasting occipital “cough” headache, dizziness, and gait impairment; in children younger than 3 years, oropharyngeal symptoms are prevalent (sleep apnea, feeding problems) whereas in those older than 3 years, a higher incidence of cough headache and scoliosis is reported. CM1 clinical features, both in children and in adults, have in common the presence of anatomical deformities of the brainstem and cerebellum. Clinical myelopathy (sensory/autonomic disorders, motor weakness) can result from direct compression of the cervical spinal cord by the herniated cerebellar tonsils or can be due to the presence of a syrinx, reported in association with Chiari I between 35 and 75% of pediatric patients. Similarly, in our series (440 females, 160 males, 98% > 18 years), syringomyelia associated with Chiari I was ranging from 40 to 60% (respectively in asymptomatic and symptomatic groups); headache was reported in 65%. Sensory disturbances (48%), cranial nerve deficits (45%), motor weakness (32%), and autonomic disorders (35%) were the most frequent neurological signs in our cohort. In Chiari I malformation, cervical pain and occipital cough headache are the most characteristic presenting symptoms, both in old children and in adults; however, headache is often multifactorial, and CM1 patients can report a wide variety of non-specific symptoms and signs. Clinical diagnostic CM1 criteria, shared at the national and international level, are recommended with the aim to avoid consequent controversies on diagnosis and on surgical decision making.
Literature
1.
go back to reference Meadows J, Kraut M, Guarneri M et al (2000) Asymptomatic Chiari type I malformations identified on magnetic resonance imaging. J Neurosurg 92(6):920–926CrossRef Meadows J, Kraut M, Guarneri M et al (2000) Asymptomatic Chiari type I malformations identified on magnetic resonance imaging. J Neurosurg 92(6):920–926CrossRef
2.
go back to reference Wu YW, Chin CT, Chan KM et al (1999) Pediatric Chiari I malformations: do clinical and radiologic features correlate? Neurology 25:221–226 Wu YW, Chin CT, Chan KM et al (1999) Pediatric Chiari I malformations: do clinical and radiologic features correlate? Neurology 25:221–226
3.
go back to reference Genitori L, Peretta P, Nurisso C, Macinante L, Mussa F (2000) Chiari type I anomalies in children and adolescents: minimally invasive management in a series of 53 cases. Childs Nerv Syst 16:707–718CrossRefPubMed Genitori L, Peretta P, Nurisso C, Macinante L, Mussa F (2000) Chiari type I anomalies in children and adolescents: minimally invasive management in a series of 53 cases. Childs Nerv Syst 16:707–718CrossRefPubMed
4.
go back to reference Park JK, Langham Gleason P, Madsen JR, Goumnerova LC, Scott M (1997) Presentation and management of Chiari I malformation in children. Pedriatr Neurosurg 26:190–196CrossRef Park JK, Langham Gleason P, Madsen JR, Goumnerova LC, Scott M (1997) Presentation and management of Chiari I malformation in children. Pedriatr Neurosurg 26:190–196CrossRef
5.
go back to reference Milhorat TH, Chou MW, Trinidad EM, Kula RW, Mandell M, Wolpert C, Speer MC (1999) Chiari I malformation redefined: clinical and radiographic findings for 364 symptomatic patients. Neurosurgery 44:1005–1117CrossRef Milhorat TH, Chou MW, Trinidad EM, Kula RW, Mandell M, Wolpert C, Speer MC (1999) Chiari I malformation redefined: clinical and radiographic findings for 364 symptomatic patients. Neurosurgery 44:1005–1117CrossRef
6.
go back to reference Tubbs RS, Mc Girt MJ, Oakes WJ (2003) Surgical experience in 130 pediatric patients with Chiari I malformation. J Neurosurg 99(2):291–296CrossRef Tubbs RS, Mc Girt MJ, Oakes WJ (2003) Surgical experience in 130 pediatric patients with Chiari I malformation. J Neurosurg 99(2):291–296CrossRef
7.
go back to reference Attenello FJ, McGirt MJ, Gathinji M et al (2008) Outcome of Chiari-associated syringomyelia after hindbrain decompression in children: analysis of 49 consecutive cases. Neurosurgery 62(6):1307–1313CrossRefPubMed Attenello FJ, McGirt MJ, Gathinji M et al (2008) Outcome of Chiari-associated syringomyelia after hindbrain decompression in children: analysis of 49 consecutive cases. Neurosurgery 62(6):1307–1313CrossRefPubMed
8.
go back to reference Tubbs RS, Beckman J, Naftel RP, Chern JJ, Wellons JC, Rozzelle CJ, Blount JP, Oakes WJ (2011) Institutional experience with 500 cases of surgically treated pediatric Chiari malformation type I. J Neurosurg Pediatr 7(3):248–256CrossRefPubMed Tubbs RS, Beckman J, Naftel RP, Chern JJ, Wellons JC, Rozzelle CJ, Blount JP, Oakes WJ (2011) Institutional experience with 500 cases of surgically treated pediatric Chiari malformation type I. J Neurosurg Pediatr 7(3):248–256CrossRefPubMed
9.
go back to reference Greenlee JD, Donovan KA, Hasan DM et al (2001) Pediatrics 110(6):1212–1219CrossRef Greenlee JD, Donovan KA, Hasan DM et al (2001) Pediatrics 110(6):1212–1219CrossRef
10.
go back to reference Tubbs RS, Lyerly MJ, Loukas M, Shoja MM, Oakes WJ (2007) The pediatric Chiari I malformation: a review. Childs Nerv Syst 23:1239–1250CrossRefPubMed Tubbs RS, Lyerly MJ, Loukas M, Shoja MM, Oakes WJ (2007) The pediatric Chiari I malformation: a review. Childs Nerv Syst 23:1239–1250CrossRefPubMed
11.
go back to reference Furtado SV, Thakar S, Hedge AS (2011) Correlation of functional outcome and natural history with clinic-radiological factors in surgically managed pediatric Chiari I malformation. Neurosurgery 68:319–328CrossRefPubMed Furtado SV, Thakar S, Hedge AS (2011) Correlation of functional outcome and natural history with clinic-radiological factors in surgically managed pediatric Chiari I malformation. Neurosurgery 68:319–328CrossRefPubMed
12.
go back to reference Headache Classification Committee of the International Headache Society-HIS (2018) The International Classification of Headache Disorders, 3rd edition. Cephalalgia 38(1):110 Headache Classification Committee of the International Headache Society-HIS (2018) The International Classification of Headache Disorders, 3rd edition. Cephalalgia 38(1):110
13.
go back to reference Pascual J, Oterino A, Berciano J (1992) Headache in type I Chiari malformation. Neurology 42:1519–1521CrossRefPubMed Pascual J, Oterino A, Berciano J (1992) Headache in type I Chiari malformation. Neurology 42:1519–1521CrossRefPubMed
14.
go back to reference Grangeon L et al (2017) Predictive factors of headache resolution after Chiari type I malformation surgery. World Neurosurgery 110:e60–e66CrossRefPubMed Grangeon L et al (2017) Predictive factors of headache resolution after Chiari type I malformation surgery. World Neurosurgery 110:e60–e66CrossRefPubMed
15.
go back to reference Paul KS, Lye RH, Strang FA, Dutton J (1983) Arnold-Chiari malformation. Review of 71 cases. J Neurosurg 58:183–187CrossRefPubMed Paul KS, Lye RH, Strang FA, Dutton J (1983) Arnold-Chiari malformation. Review of 71 cases. J Neurosurg 58:183–187CrossRefPubMed
16.
go back to reference Pasquis P et al (1998) Chiari type I malformation and syringomyelia in unrelated patients with blepharophimosis. Report of two cases. J Neurosurg 89:835–838CrossRef Pasquis P et al (1998) Chiari type I malformation and syringomyelia in unrelated patients with blepharophimosis. Report of two cases. J Neurosurg 89:835–838CrossRef
17.
go back to reference Pettorini BL, Oesman C, Magdum S (2010) New presenting symptoms of Chiari I malformation: report of two cases. Childs Nerv Syst 26:399–402CrossRefPubMed Pettorini BL, Oesman C, Magdum S (2010) New presenting symptoms of Chiari I malformation: report of two cases. Childs Nerv Syst 26:399–402CrossRefPubMed
18.
go back to reference Sivakanthan S, Goldhagen C, Danner C, Agazzi S (2014) Hearing loss and Chiari malformation: a clinical pearl. Clin Neurol Neurosurg 122:20–22CrossRefPubMed Sivakanthan S, Goldhagen C, Danner C, Agazzi S (2014) Hearing loss and Chiari malformation: a clinical pearl. Clin Neurol Neurosurg 122:20–22CrossRefPubMed
19.
go back to reference Massimi L, Della Pepa GM, Tamburrini G et al (2011) Sudden onset of Chiari malformation type I in previously asymptomatic patients. J Neurosurg Pediatr 8(5):438–442CrossRefPubMed Massimi L, Della Pepa GM, Tamburrini G et al (2011) Sudden onset of Chiari malformation type I in previously asymptomatic patients. J Neurosurg Pediatr 8(5):438–442CrossRefPubMed
20.
go back to reference Miranda SP, Kimmel KT, Silberstein HJ (2016) Acute presentation of Chiari I malformation with hemiparesis in a pediatric patient. World Neurosurgery 85:366.e1–366.e4CrossRef Miranda SP, Kimmel KT, Silberstein HJ (2016) Acute presentation of Chiari I malformation with hemiparesis in a pediatric patient. World Neurosurgery 85:366.e1–366.e4CrossRef
21.
go back to reference Lewis AR, Kline LB, Sharpe JA (1996) Aquired esotropia due to Arnold-Chiari malformation. J Neuroophthalmol 16:49–54CrossRefPubMed Lewis AR, Kline LB, Sharpe JA (1996) Aquired esotropia due to Arnold-Chiari malformation. J Neuroophthalmol 16:49–54CrossRefPubMed
22.
go back to reference Almotairi FS, Andersson M, Andersson O, Skoglund T, Tisell M (2018) Swallowing dysfunction in adult patients with Chiari I malformation. J Neurol Surg 79:606–613CrossRef Almotairi FS, Andersson M, Andersson O, Skoglund T, Tisell M (2018) Swallowing dysfunction in adult patients with Chiari I malformation. J Neurol Surg 79:606–613CrossRef
23.
go back to reference Isu T, Iwasaki Y, Akino M, Abe H (1990) Syringomyelia associated with a Chiari I malformation in children and adolescents. Neurosurgery 26(4):591–596CrossRefPubMed Isu T, Iwasaki Y, Akino M, Abe H (1990) Syringomyelia associated with a Chiari I malformation in children and adolescents. Neurosurgery 26(4):591–596CrossRefPubMed
24.
go back to reference Isu T, Chono Y, Iwasaki Y, Koyanagi I, Akino M, Abe H, Abumi K, Kaneda K (1992) Scoliosis associated with syringomyelia presentingin children. Childs Nerv Syst 8(2):97–100CrossRefPubMed Isu T, Chono Y, Iwasaki Y, Koyanagi I, Akino M, Abe H, Abumi K, Kaneda K (1992) Scoliosis associated with syringomyelia presentingin children. Childs Nerv Syst 8(2):97–100CrossRefPubMed
25.
go back to reference Oakes J, Thompson D (2014) Paediatric perspectives. In: Flint G, Rusbridge C (eds) Syringomyelia. Springer-Verlag, Berlin, pp 193–2017CrossRef Oakes J, Thompson D (2014) Paediatric perspectives. In: Flint G, Rusbridge C (eds) Syringomyelia. Springer-Verlag, Berlin, pp 193–2017CrossRef
27.
28.
go back to reference Ciaramitaro P, Baldovino S, Roccatello D et al (2011) Chiari and syringomyelia consortium: a model of multidisciplinary and sharing path for rare diseases. Neurol Sci 32 (Suppl.3:S271–S272CrossRefPubMed Ciaramitaro P, Baldovino S, Roccatello D et al (2011) Chiari and syringomyelia consortium: a model of multidisciplinary and sharing path for rare diseases. Neurol Sci 32 (Suppl.3:S271–S272CrossRefPubMed
29.
go back to reference Taylor RF, Larkins MV (2002) Headache and Chiari I malformation: clinical presentation, diagnosis and controversies in management. Current Pain Headache Reports 6:331–337CrossRefPubMed Taylor RF, Larkins MV (2002) Headache and Chiari I malformation: clinical presentation, diagnosis and controversies in management. Current Pain Headache Reports 6:331–337CrossRefPubMed
30.
go back to reference Scelsa SN (2000) Syringomyelia presenting as ulnar neuropathy at the elbow. Clin Neurophysiol 111:1527–1530CrossRefPubMed Scelsa SN (2000) Syringomyelia presenting as ulnar neuropathy at the elbow. Clin Neurophysiol 111:1527–1530CrossRefPubMed
Metadata
Title
Clinical diagnosis—part I: what is really caused by Chiari I
Authors
Palma Ciaramitaro
Marilena Ferraris
Fulvio Massaro
Diego Garbossa
Publication date
01-10-2019
Publisher
Springer Berlin Heidelberg
Published in
Child's Nervous System / Issue 10/2019
Print ISSN: 0256-7040
Electronic ISSN: 1433-0350
DOI
https://doi.org/10.1007/s00381-019-04206-z

Other articles of this Issue 10/2019

Child's Nervous System 10/2019 Go to the issue