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Erschienen in: Child's Nervous System 10/2011

01.10.2011 | Special Annual Issue

Hydrocephalus and Chiari type I malformation

verfasst von: Concezio Di Rocco, Paolo Frassanito, Luca Massimi, Simone Peraio

Erschienen in: Child's Nervous System | Ausgabe 10/2011

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Abstract

Intoduction

Hydrocephalus has been related to Chiari type I malformation (CIM) for a long time. The pathogenesis of this association is complex and still debated.

Discussion

A supratentorial hypertensive hydrocephalus may cause CIM, exerting pressure from above. Another pathogenetic hypothesis is based on the clinical and radiological data from patients affected by complex craniosynostosis, in which this association is more commonly observed as the consequence of a “cephalo-cranial disproportion” ultimately leading to a secondary hydrocephalus. In some cases, the concomitant presence of a stenosis of the jugular foramina would determine a condition of upward venous hypertension, resulting in the development of CIM and an associated hydrocephalus due to cerebellar parenchyma turgor.

Conclusions

The radiological association of ventricular enlargement and hindbrain herniation would be the result of heterogeneous pathogenetic mechanisms which would then require specific therapeutic approaches. In this context, the endoscopic third ventricle-cisternostomy is gaining an increasing interest because of its more physiologic correction of the altered CSF dynamics and its minor interference on the developmental processes responsible for the association of hydrocephalus and CIM.
Literatur
1.
Zurück zum Zitat Amacher AL, Page LK (1971) Hydrocephalus due to membranous obstruction of the fourth ventricle. J Neurosurg 35(6):672–676PubMedCrossRef Amacher AL, Page LK (1971) Hydrocephalus due to membranous obstruction of the fourth ventricle. J Neurosurg 35(6):672–676PubMedCrossRef
2.
Zurück zum Zitat Banik R, Lin D, Miller NR (2006) Prevalence of Chiari I malformation and cerebellar ectopia in patients with pseudotumor cerebri. J Neurol Sci 247(1):71–75PubMedCrossRef Banik R, Lin D, Miller NR (2006) Prevalence of Chiari I malformation and cerebellar ectopia in patients with pseudotumor cerebri. J Neurol Sci 247(1):71–75PubMedCrossRef
3.
Zurück zum Zitat Bejjani GK (2003) Association of the adult Chiari malformation and idiopathic intracranial hypertension: more than a coincidence. Med Hypotheses 60(6):859–863PubMedCrossRef Bejjani GK (2003) Association of the adult Chiari malformation and idiopathic intracranial hypertension: more than a coincidence. Med Hypotheses 60(6):859–863PubMedCrossRef
4.
Zurück zum Zitat Britto JA, Chan JC, Evans RD, Hayward RD, Thorogood P, Jones BM (1998) Fibroblast growth factor receptors are expressed in craniosynostotic sutures. Plast Reconstr Surg 101(2):540–543PubMedCrossRef Britto JA, Chan JC, Evans RD, Hayward RD, Thorogood P, Jones BM (1998) Fibroblast growth factor receptors are expressed in craniosynostotic sutures. Plast Reconstr Surg 101(2):540–543PubMedCrossRef
5.
Zurück zum Zitat Caldarelli M, Novegno F, Di Rocco C (2009) A late complication of CSF shunting: acquired Chiari I malformation. Childs Nerv Syst 25(4):443–452PubMedCrossRef Caldarelli M, Novegno F, Di Rocco C (2009) A late complication of CSF shunting: acquired Chiari I malformation. Childs Nerv Syst 25(4):443–452PubMedCrossRef
6.
Zurück zum Zitat Chiari H (1891) Uber Veränderungen des Kleinhirns infolge von Hydrocephalie des Grosshirns. Dtsch Med Wochenschr 17:1172–1175CrossRef Chiari H (1891) Uber Veränderungen des Kleinhirns infolge von Hydrocephalie des Grosshirns. Dtsch Med Wochenschr 17:1172–1175CrossRef
7.
Zurück zum Zitat Cinalli G, Renier D, Sebag G, Sainte-Rose C, Arnaud E, Pierre-Khan A (1995) Chronic tonsillar herniation in Crouzon’s and Apert’s syndromes: the role of premature synostosis of the lambdoid suture. J Neurosurg 83(4):575–582PubMedCrossRef Cinalli G, Renier D, Sebag G, Sainte-Rose C, Arnaud E, Pierre-Khan A (1995) Chronic tonsillar herniation in Crouzon’s and Apert’s syndromes: the role of premature synostosis of the lambdoid suture. J Neurosurg 83(4):575–582PubMedCrossRef
8.
Zurück zum Zitat Cinalli G, Sainte-Rose C, Kollar E, Arnaud E, Renier D (1998) Hydrocephalus and craniosynostosis. J Neurosurg 88(2):209–214PubMedCrossRef Cinalli G, Sainte-Rose C, Kollar E, Arnaud E, Renier D (1998) Hydrocephalus and craniosynostosis. J Neurosurg 88(2):209–214PubMedCrossRef
9.
Zurück zum Zitat Cinalli G, Spennato P, Sainte-Rose C, Arnaud E, Aliberti F, Brunelle F, Cianciulli E, Renier D (2005) Chiari malformation in craniosynostosis. Childs Nerv Syst 21(10):889–901PubMedCrossRef Cinalli G, Spennato P, Sainte-Rose C, Arnaud E, Aliberti F, Brunelle F, Cianciulli E, Renier D (2005) Chiari malformation in craniosynostosis. Childs Nerv Syst 21(10):889–901PubMedCrossRef
10.
Zurück zum Zitat Decq P, Le Guérinel C, Sol JC, Brugières P, Djindjian M, Nguyen JP (2001) Chiari I malformation: a rare cause of noncommunicating hydrocephalus treated by third ventriculostomy. J Neurosurg 95(5):783–790PubMedCrossRef Decq P, Le Guérinel C, Sol JC, Brugières P, Djindjian M, Nguyen JP (2001) Chiari I malformation: a rare cause of noncommunicating hydrocephalus treated by third ventriculostomy. J Neurosurg 95(5):783–790PubMedCrossRef
11.
Zurück zum Zitat Di Rocco C, Di Trapani G, Pettorossi VE, Caldarelli M (1979) On the pathology of experimental hydrocephalus induced by artificial increase in endoventricular CSF pulse pressare. Childs Brain 5(2):81–95PubMed Di Rocco C, Di Trapani G, Pettorossi VE, Caldarelli M (1979) On the pathology of experimental hydrocephalus induced by artificial increase in endoventricular CSF pulse pressare. Childs Brain 5(2):81–95PubMed
12.
Zurück zum Zitat Di Rocco C, Maira G, Rossi GF, Vignati A (1976) Cerebrospinal fluid pressare studies in normal pressare hydrocephalus and cerebral atrophy. Eur Neurol 14(2):119–128PubMedCrossRef Di Rocco C, Maira G, Rossi GF, Vignati A (1976) Cerebrospinal fluid pressare studies in normal pressare hydrocephalus and cerebral atrophy. Eur Neurol 14(2):119–128PubMedCrossRef
13.
Zurück zum Zitat Di Rocco C, Massimi L, Tamburrini G (2006) Shunts vs endoscopic third ventriculostomy in infants: are there different types and/or rates of complications? A review. Childs Nerv Syst 22(12):1573–1589PubMedCrossRef Di Rocco C, Massimi L, Tamburrini G (2006) Shunts vs endoscopic third ventriculostomy in infants: are there different types and/or rates of complications? A review. Childs Nerv Syst 22(12):1573–1589PubMedCrossRef
14.
Zurück zum Zitat Di Rocco C, Rende M (1987) Neural tube defects. Some remarks on the possible role of glycosaminoglycans in the genesis of the dysraphic state, the anomaly in the configuration of the posterior cranial fossa, and hydrocephalus. Childs Nerv Syst 3(6):334–341PubMedCrossRef Di Rocco C, Rende M (1987) Neural tube defects. Some remarks on the possible role of glycosaminoglycans in the genesis of the dysraphic state, the anomaly in the configuration of the posterior cranial fossa, and hydrocephalus. Childs Nerv Syst 3(6):334–341PubMedCrossRef
15.
Zurück zum Zitat Di Rocco F, Jucá CE, Arnaud E, Renier D, Sainte-Rose C (2010) The role of endoscopic third ventriculostomy in the treatment of hydrocephalus associated with faciocraniosynostosis. J Neurosurg Pediatr 6(1):17–22PubMedCrossRef Di Rocco F, Jucá CE, Arnaud E, Renier D, Sainte-Rose C (2010) The role of endoscopic third ventriculostomy in the treatment of hydrocephalus associated with faciocraniosynostosis. J Neurosurg Pediatr 6(1):17–22PubMedCrossRef
16.
Zurück zum Zitat Di Rocco C, Pettorossi VE, Caldarelli M, Mancinelli R, Velardi F (1978) Communicating hydrocephalus induced by mechanically increased amplitude of the intraventricular cerebrospinal fluid pressure: experimental studies. Exp Neurol 59(1):40–52PubMedCrossRef Di Rocco C, Pettorossi VE, Caldarelli M, Mancinelli R, Velardi F (1978) Communicating hydrocephalus induced by mechanically increased amplitude of the intraventricular cerebrospinal fluid pressure: experimental studies. Exp Neurol 59(1):40–52PubMedCrossRef
17.
Zurück zum Zitat Du Bulay G, Shah SH, Currie JC, Logne V (1974) The mechanism of hydromyelia in Chiari type I malformation. Br J Radiol 47(561):579–587CrossRef Du Bulay G, Shah SH, Currie JC, Logne V (1974) The mechanism of hydromyelia in Chiari type I malformation. Br J Radiol 47(561):579–587CrossRef
18.
Zurück zum Zitat Elster AD, Chen MY (1992) Chiari I malformations: clinical and radiological reappraisal. Radiology 183(2):347–353PubMed Elster AD, Chen MY (1992) Chiari I malformations: clinical and radiological reappraisal. Radiology 183(2):347–353PubMed
19.
Zurück zum Zitat Ersahin Y, Gokcay A (2002) Acquired Chiari I malformation changes postendoscopic third ventriculostomy. Pediatr Neurosurg 36(1):54PubMedCrossRef Ersahin Y, Gokcay A (2002) Acquired Chiari I malformation changes postendoscopic third ventriculostomy. Pediatr Neurosurg 36(1):54PubMedCrossRef
20.
Zurück zum Zitat Fagan LH, Ferguson S, Yassari R, Frim DM (2006) The Chiari pseudotumor cerebri syndrome: symptom recurrence after decompressive surgery for Chiari malformation type I. Pediatr Neurosurg 42(1):14–19PubMedCrossRef Fagan LH, Ferguson S, Yassari R, Frim DM (2006) The Chiari pseudotumor cerebri syndrome: symptom recurrence after decompressive surgery for Chiari malformation type I. Pediatr Neurosurg 42(1):14–19PubMedCrossRef
21.
Zurück zum Zitat Francis PM, Beals S, Rekate HL, Pittman HW, Manwaring K, Reiff J (1992) Chronic tonsillar herniation and Crouzon’s syndrome. Pediatr Neurosurg 18(4):202–206PubMedCrossRef Francis PM, Beals S, Rekate HL, Pittman HW, Manwaring K, Reiff J (1992) Chronic tonsillar herniation and Crouzon’s syndrome. Pediatr Neurosurg 18(4):202–206PubMedCrossRef
22.
Zurück zum Zitat Fukuhara T, Vorster SJ, Luciano MG (2000) Risk factors for failure endoscopic third ventriculostomy for obstructive hydrocephalus. Neurosurgery 46(5):1100–1111PubMedCrossRef Fukuhara T, Vorster SJ, Luciano MG (2000) Risk factors for failure endoscopic third ventriculostomy for obstructive hydrocephalus. Neurosurgery 46(5):1100–1111PubMedCrossRef
23.
Zurück zum Zitat Grabb P, Mapstone T, Oakes WJ (1999) Ventral brainstem compression in pediatric and young adult patients with Chiari I malformations. Neurosurgery 44(3):520–528PubMedCrossRef Grabb P, Mapstone T, Oakes WJ (1999) Ventral brainstem compression in pediatric and young adult patients with Chiari I malformations. Neurosurgery 44(3):520–528PubMedCrossRef
24.
Zurück zum Zitat Gray JL, Kang SS, Zenni GC, Kim DU, Kim PI, Burgess WH, Drohan W, Winkles JA, Haudenschild CC, Greisler HP (1994) FGF-1 affixation stimulates ePTFE endothelialization without intimal hyperplasia. J Surg Res 57(5):596–612PubMedCrossRef Gray JL, Kang SS, Zenni GC, Kim DU, Kim PI, Burgess WH, Drohan W, Winkles JA, Haudenschild CC, Greisler HP (1994) FGF-1 affixation stimulates ePTFE endothelialization without intimal hyperplasia. J Surg Res 57(5):596–612PubMedCrossRef
25.
Zurück zum Zitat Gripp KW, Hopkins E, Doyle D, Dobyns WB (2010) High incidence of progressive postnatal cerebellar enlargement in Costello syndrome: brain overgrowth associated with HRAS mutations as the likely cause of structural brain and spinal cord abnormalities. Am J Med Genet 152A(5):1161–1168PubMedCrossRef Gripp KW, Hopkins E, Doyle D, Dobyns WB (2010) High incidence of progressive postnatal cerebellar enlargement in Costello syndrome: brain overgrowth associated with HRAS mutations as the likely cause of structural brain and spinal cord abnormalities. Am J Med Genet 152A(5):1161–1168PubMedCrossRef
26.
Zurück zum Zitat Hackel M, Benes V, Mohapl M (2001) Simultaneous cerebral and spinal fluid pressure recordings in surgical indications of the Chiari malformation without myelodysplasia. Acta Neurochir 143(9):909–918CrossRef Hackel M, Benes V, Mohapl M (2001) Simultaneous cerebral and spinal fluid pressure recordings in surgical indications of the Chiari malformation without myelodysplasia. Acta Neurochir 143(9):909–918CrossRef
27.
Zurück zum Zitat Hashish H, Guenot M, Mertens P, Sindou M (1999) Hydrocéphalie chronique de l’adulte par occlusion membranaire congénitale de l’ouverture médiane du quatrième ventricule (Foramen de Magendie). Rapport de deux cas et revue de la literature. Neurochirurgie 45(3):232–236PubMed Hashish H, Guenot M, Mertens P, Sindou M (1999) Hydrocéphalie chronique de l’adulte par occlusion membranaire congénitale de l’ouverture médiane du quatrième ventricule (Foramen de Magendie). Rapport de deux cas et revue de la literature. Neurochirurgie 45(3):232–236PubMed
28.
Zurück zum Zitat Hayhurst C, Osman-Farah J, Das K, Mallucci C (2008) Initial management of hydrocephalus associate with Chiari malformation type I-syringomyelia complex via endoscopic third ventriculostomy: an outcome analysis. J Neurosurg 108(6):1211–1214PubMedCrossRef Hayhurst C, Osman-Farah J, Das K, Mallucci C (2008) Initial management of hydrocephalus associate with Chiari malformation type I-syringomyelia complex via endoscopic third ventriculostomy: an outcome analysis. J Neurosurg 108(6):1211–1214PubMedCrossRef
29.
Zurück zum Zitat Hoffman HJ, Tucker WS (1976) Cephalocranial disproportion. A complication of the treatment of hydrocephalus in children. Childs Brain 2(3):167–176PubMed Hoffman HJ, Tucker WS (1976) Cephalocranial disproportion. A complication of the treatment of hydrocephalus in children. Childs Brain 2(3):167–176PubMed
30.
Zurück zum Zitat Hofmann E, Warmuth-Metz M, Bendszus M, Solymosi L (2000) Phase-contrast MR imaging of the cervical CSF and spinal cord: volumetric motion analysis in patients with Chiari I malformation. AJNR 21(1):151–158PubMed Hofmann E, Warmuth-Metz M, Bendszus M, Solymosi L (2000) Phase-contrast MR imaging of the cervical CSF and spinal cord: volumetric motion analysis in patients with Chiari I malformation. AJNR 21(1):151–158PubMed
31.
Zurück zum Zitat Holder-Espinasse M, Winter RM (2003) Type 1 Chiari malformation and Noonan syndrome: a new diagnostic feature? Clin Dysmorphol 12(4):275PubMedCrossRef Holder-Espinasse M, Winter RM (2003) Type 1 Chiari malformation and Noonan syndrome: a new diagnostic feature? Clin Dysmorphol 12(4):275PubMedCrossRef
32.
Zurück zum Zitat Kandasamy J, Kneen R, Gladstone M, Newman W, Mohamed T, Mallucci C (2008) Chiari I malformation without hydrocephalus: acute intracranial hypertension managed with endoscopic third ventriculostomy. Childs Nerv Syst 24(12):1493–1497PubMedCrossRef Kandasamy J, Kneen R, Gladstone M, Newman W, Mohamed T, Mallucci C (2008) Chiari I malformation without hydrocephalus: acute intracranial hypertension managed with endoscopic third ventriculostomy. Childs Nerv Syst 24(12):1493–1497PubMedCrossRef
33.
Zurück zum Zitat Kratz CP, Zampino G, Kriek M, Kant SG, Leoni C, Pantaleoni F, Oudesluys-Murphy AM, Di Rocco C, Kloska SP, Tartaglia M, Zenker M (2009) Craniosynostosis in patients with Noonan syndrome caused by germline KRAS mutations. Am J Med Genet A 149A(5):1036–1040PubMedCrossRef Kratz CP, Zampino G, Kriek M, Kant SG, Leoni C, Pantaleoni F, Oudesluys-Murphy AM, Di Rocco C, Kloska SP, Tartaglia M, Zenker M (2009) Craniosynostosis in patients with Noonan syndrome caused by germline KRAS mutations. Am J Med Genet A 149A(5):1036–1040PubMedCrossRef
34.
Zurück zum Zitat Kreiborg S, Marsh JL, Cohen MM Jr, Liversage M, Pedersen H, Skovby F, Borgesen SE, Vannier MW (1993) Comparative three-dimensional analysis of CT-scans of the calvaria and cranial base in Apert and Crouzon syndrome. J Craniomaxillofac Surg 21(5):181–188PubMed Kreiborg S, Marsh JL, Cohen MM Jr, Liversage M, Pedersen H, Skovby F, Borgesen SE, Vannier MW (1993) Comparative three-dimensional analysis of CT-scans of the calvaria and cranial base in Apert and Crouzon syndrome. J Craniomaxillofac Surg 21(5):181–188PubMed
35.
Zurück zum Zitat Lee M, Rezai AR, Wisoff JH (1995) Acquired Chiari I malformation and hydromyelia secondary to a giant craniopharingioma. Pediatr Neurosurg 22(5):251–254PubMedCrossRef Lee M, Rezai AR, Wisoff JH (1995) Acquired Chiari I malformation and hydromyelia secondary to a giant craniopharingioma. Pediatr Neurosurg 22(5):251–254PubMedCrossRef
36.
Zurück zum Zitat Lemire RJ, Loeser JD, Leech RW (1975) Normal and abnormal development of the human nervous system. Harper and Row, Hagerstown, pp 95–108 Lemire RJ, Loeser JD, Leech RW (1975) Normal and abnormal development of the human nervous system. Harper and Row, Hagerstown, pp 95–108
37.
Zurück zum Zitat Marin-Padilla M, Marin-Padilla TM (1981) Morphogenesis of experimentally induced Arnold-Chiari malformation. J Neurol Sci 50(1):29–55PubMedCrossRef Marin-Padilla M, Marin-Padilla TM (1981) Morphogenesis of experimentally induced Arnold-Chiari malformation. J Neurol Sci 50(1):29–55PubMedCrossRef
38.
Zurück zum Zitat Martinez-Lage JF, Guillén-Navarro E, Almagro MJ, Felipe-Murcia M, López López-Guerrero A, Galarza M (2010) Hydrocephalus and Chiari type 1 malformation in macrocephaly cutis marmorata telangiectatica congenita: a case-based update. Childs Nerv Syst 26(1):13–18PubMedCrossRef Martinez-Lage JF, Guillén-Navarro E, Almagro MJ, Felipe-Murcia M, López López-Guerrero A, Galarza M (2010) Hydrocephalus and Chiari type 1 malformation in macrocephaly cutis marmorata telangiectatica congenita: a case-based update. Childs Nerv Syst 26(1):13–18PubMedCrossRef
39.
Zurück zum Zitat Martinez-Perez D, Vander Woude DL, Barnes PD, Scott RM, Mulliken JB (1996) Jugular foraminal stenosis in Crouzon syndrome. Pediatr Neurosurg 25(5):252–255PubMedCrossRef Martinez-Perez D, Vander Woude DL, Barnes PD, Scott RM, Mulliken JB (1996) Jugular foraminal stenosis in Crouzon syndrome. Pediatr Neurosurg 25(5):252–255PubMedCrossRef
40.
Zurück zum Zitat Massimi L, Novegno F, Di Rocco C (2011) Chiari Type 1 malformation in children. In: Pickard JD (ed) Advances and technical standards in neurosurgery. Springer Verlag, Wien, Vol. 37 (ahead of print) Massimi L, Novegno F, Di Rocco C (2011) Chiari Type 1 malformation in children. In: Pickard JD (ed) Advances and technical standards in neurosurgery. Springer Verlag, Wien, Vol. 37 (ahead of print)
41.
Zurück zum Zitat Massimi L, Pravatà E, Tamburrini G, Gaudino S, Pettorini B, Novegno F, Colosimo C Jr, Di Rocco C (2011) Endoscopic third ventriculostomy for the management of Chiari I and related hydrocephalus: outcome and pathogenetic implications. Neurosurgery 68:950–956PubMed Massimi L, Pravatà E, Tamburrini G, Gaudino S, Pettorini B, Novegno F, Colosimo C Jr, Di Rocco C (2011) Endoscopic third ventriculostomy for the management of Chiari I and related hydrocephalus: outcome and pathogenetic implications. Neurosurgery 68:950–956PubMed
42.
Zurück zum Zitat Metellus P, Dufour H, Levrier O, Grisoli F (2002) Endoscopic third ventriculostomy for treatment of noncommunicating syringomyelia associated with a Chiari I malformation and hydrocephalus: case report and pathophysiological considerations. Neurosurgery 51(2):500–503PubMedCrossRef Metellus P, Dufour H, Levrier O, Grisoli F (2002) Endoscopic third ventriculostomy for treatment of noncommunicating syringomyelia associated with a Chiari I malformation and hydrocephalus: case report and pathophysiological considerations. Neurosurgery 51(2):500–503PubMedCrossRef
43.
Zurück zum Zitat Milhorat TH, Chou MW, Trinidad EM (1999) Chiari I malformation redefined clinical and radiographic findings for 364 symptomatic patients. Neurosurgery 44(5):1005–1017PubMedCrossRef Milhorat TH, Chou MW, Trinidad EM (1999) Chiari I malformation redefined clinical and radiographic findings for 364 symptomatic patients. Neurosurgery 44(5):1005–1017PubMedCrossRef
44.
Zurück zum Zitat Mohanty A, Suman R, Shankar SR, Satish S, Shankar Praharaj S (2005) Endoscopic third ventriculostomy in the management of Chiari I malformation and syringomyelia associated with hydrocephalus. Clin Neurol Neurosurg 108(1):87–92PubMedCrossRef Mohanty A, Suman R, Shankar SR, Satish S, Shankar Praharaj S (2005) Endoscopic third ventriculostomy in the management of Chiari I malformation and syringomyelia associated with hydrocephalus. Clin Neurol Neurosurg 108(1):87–92PubMedCrossRef
45.
Zurück zum Zitat Nishihara T, Hara T, Suzuki I, Kirino T, Yamakawa K (1996) Third ventriculostomy for symptomatic syringomyelia using flexible endoscope: case report. Minim Invasive Neurosurg 39(4):130–132PubMedCrossRef Nishihara T, Hara T, Suzuki I, Kirino T, Yamakawa K (1996) Third ventriculostomy for symptomatic syringomyelia using flexible endoscope: case report. Minim Invasive Neurosurg 39(4):130–132PubMedCrossRef
46.
Zurück zum Zitat Nishikawa M, Sakamoto H, Hakuba A, Nakanishi N, Inoue Y (1997) Pathogenesis of Chiari malformation: a morphometric study o the posterior cranial fossa. J Neurosurg 86(1):40–47PubMedCrossRef Nishikawa M, Sakamoto H, Hakuba A, Nakanishi N, Inoue Y (1997) Pathogenesis of Chiari malformation: a morphometric study o the posterior cranial fossa. J Neurosurg 86(1):40–47PubMedCrossRef
47.
Zurück zum Zitat Okudera T, Huang YP, Ohta T, Yokota A, Nakamura Y, Maehara F, Utsunomiya H, Uemura K, Fukasawa H (1994) Development of posterior fossa dural sinuses, emissary veins, and jugular bulb: morphological and radiologic study. Am J Neuroradiol 15(10):1871–1883PubMed Okudera T, Huang YP, Ohta T, Yokota A, Nakamura Y, Maehara F, Utsunomiya H, Uemura K, Fukasawa H (1994) Development of posterior fossa dural sinuses, emissary veins, and jugular bulb: morphological and radiologic study. Am J Neuroradiol 15(10):1871–1883PubMed
48.
Zurück zum Zitat Osuagwu FC, Lazareff JA, Rahman S, Bash S (2005) Chiari I anatomy after ventriculoperitoneal shunting:posterior fossa volumetric evaluation with MRI. Childs Nerv Syst 22(11):1451–1456CrossRef Osuagwu FC, Lazareff JA, Rahman S, Bash S (2005) Chiari I anatomy after ventriculoperitoneal shunting:posterior fossa volumetric evaluation with MRI. Childs Nerv Syst 22(11):1451–1456CrossRef
49.
Zurück zum Zitat Park JK, Gleason PL, Madsen JR, Goumnerova LC, Scott RM (1997) Presentation and management of Chiari I malformation in children. Pediatr Neurosurg 26(4):190–196PubMedCrossRef Park JK, Gleason PL, Madsen JR, Goumnerova LC, Scott RM (1997) Presentation and management of Chiari I malformation in children. Pediatr Neurosurg 26(4):190–196PubMedCrossRef
50.
Zurück zum Zitat Rifkinson-Mann S, Sachdev VP, Huang YP (1987) Congenital fourth ventricular midline outlet obstruction. Report of two cases. J Neurosurg 67(4):595–599PubMedCrossRef Rifkinson-Mann S, Sachdev VP, Huang YP (1987) Congenital fourth ventricular midline outlet obstruction. Report of two cases. J Neurosurg 67(4):595–599PubMedCrossRef
51.
Zurück zum Zitat Saldino RM, Steinbach HL, Epstein CJ (1972) Familial acrocephalosyndactily (Pfeiffer syndrome). Am J Roentgenol 116(3):609–622 Saldino RM, Steinbach HL, Epstein CJ (1972) Familial acrocephalosyndactily (Pfeiffer syndrome). Am J Roentgenol 116(3):609–622
52.
Zurück zum Zitat Schijman E, Steinbok P (2004) International survey on the management of Chiari I malformation and syringomyelia. Childs Nerv Syst 20(5):341–348PubMedCrossRef Schijman E, Steinbok P (2004) International survey on the management of Chiari I malformation and syringomyelia. Childs Nerv Syst 20(5):341–348PubMedCrossRef
53.
Zurück zum Zitat Sgouros S, Goldin JH, Hockley AD, Wake MJ (1996) Posterior skull surgery in craniosynostosis. Childs Nerv Syst 12(11):727–733PubMedCrossRef Sgouros S, Goldin JH, Hockley AD, Wake MJ (1996) Posterior skull surgery in craniosynostosis. Childs Nerv Syst 12(11):727–733PubMedCrossRef
54.
Zurück zum Zitat Sgouros S, Natarajan K, Hockley AD, Goldin JH, Wake M (1999) Skull base growth in craniosynostosis. Pediatr Neurosurg 31(6):281–293PubMedCrossRef Sgouros S, Natarajan K, Hockley AD, Goldin JH, Wake M (1999) Skull base growth in craniosynostosis. Pediatr Neurosurg 31(6):281–293PubMedCrossRef
55.
Zurück zum Zitat Sheehan JM, Jane JA Sr (2000) Resolution of tonsillar herniation and syringomyelia after supratentorial tumor resection: case report and review of the literature. Neurosurgery 47(1):233–235PubMed Sheehan JM, Jane JA Sr (2000) Resolution of tonsillar herniation and syringomyelia after supratentorial tumor resection: case report and review of the literature. Neurosurgery 47(1):233–235PubMed
56.
Zurück zum Zitat Stovner LJ, Bergan U, Nilsen G, Sjaastad O (1993) Posterior cranial fossa dimensions in the Chiari I malformation: relation to the pathogenesis and clinical presentation. Neuroradiology 35(2):113–118PubMedCrossRef Stovner LJ, Bergan U, Nilsen G, Sjaastad O (1993) Posterior cranial fossa dimensions in the Chiari I malformation: relation to the pathogenesis and clinical presentation. Neuroradiology 35(2):113–118PubMedCrossRef
57.
Zurück zum Zitat Suheiro T, Inamura T, Natori Y, Sasaki M, Fukui M (2000) Successful neuroendoscopic third ventriculostomy for hydrocephalus and syringomyelia associated with fourth ventricle outlet obstruction. J Neurosurg 93(2):326–329CrossRef Suheiro T, Inamura T, Natori Y, Sasaki M, Fukui M (2000) Successful neuroendoscopic third ventriculostomy for hydrocephalus and syringomyelia associated with fourth ventricle outlet obstruction. J Neurosurg 93(2):326–329CrossRef
58.
Zurück zum Zitat Teo C, Nakaji P, Seisier D, Coughlan M (2005) Resolution of trigeminal neuralgia following third ventriculostomy for hydrocephalus associate with Chiari I malformation: case report. Minim Invasive Neurosurg 48(5):302–305PubMedCrossRef Teo C, Nakaji P, Seisier D, Coughlan M (2005) Resolution of trigeminal neuralgia following third ventriculostomy for hydrocephalus associate with Chiari I malformation: case report. Minim Invasive Neurosurg 48(5):302–305PubMedCrossRef
59.
Zurück zum Zitat Tubbs RS, McGirt MJ, Oakes WJ (2003) Surgical experience in 130 pediatric patients with Chiari I malformation. J Neurosurg 99(2):291–296PubMedCrossRef Tubbs RS, McGirt MJ, Oakes WJ (2003) Surgical experience in 130 pediatric patients with Chiari I malformation. J Neurosurg 99(2):291–296PubMedCrossRef
60.
Zurück zum Zitat Tubbs RS, Rutledge SL, Kosentka A, Bartolucci AA, Oakes WJ (2004) Chiari I malformation and neurofibromatosis type 1. Pediatr Neurol 30(4):278–280PubMedCrossRef Tubbs RS, Rutledge SL, Kosentka A, Bartolucci AA, Oakes WJ (2004) Chiari I malformation and neurofibromatosis type 1. Pediatr Neurol 30(4):278–280PubMedCrossRef
61.
Zurück zum Zitat Tubbs RS, Lyerly MJ, Loukas M, Shoja M, Oakes WJ (2007) The pediatric Chiari I malformation: a review. Childs Nerv Syst 23(11):1239–1250PubMedCrossRef Tubbs RS, Lyerly MJ, Loukas M, Shoja M, Oakes WJ (2007) The pediatric Chiari I malformation: a review. Childs Nerv Syst 23(11):1239–1250PubMedCrossRef
62.
Zurück zum Zitat Venes JL (1988) Arnold-Chiari malformation in an infant with Kleeblattschadel: an acquired malformation. Neurosurgery 23(3):360–362PubMedCrossRef Venes JL (1988) Arnold-Chiari malformation in an infant with Kleeblattschadel: an acquired malformation. Neurosurgery 23(3):360–362PubMedCrossRef
63.
Zurück zum Zitat Williams B (1975) Cerebrospinal fluid pressure gradients in spina bifida cystic, with special reference to the Arnold-Chiari malformation and aqueductal stenosis. Dev Med Child Neurol 35:138–150 Williams B (1975) Cerebrospinal fluid pressure gradients in spina bifida cystic, with special reference to the Arnold-Chiari malformation and aqueductal stenosis. Dev Med Child Neurol 35:138–150
64.
Zurück zum Zitat Williams B (1981) Simultaneous cerebral and spinal fluid pressure recordings, 2. Cerebrospinal dissociation with lesions at the foramen magnum. Acta Neurochir 59(1–2):123–142CrossRef Williams B (1981) Simultaneous cerebral and spinal fluid pressure recordings, 2. Cerebrospinal dissociation with lesions at the foramen magnum. Acta Neurochir 59(1–2):123–142CrossRef
65.
66.
Zurück zum Zitat Williams H (2008) A unifying hypothesis for hydrocephalus, Chiari malformation, syringomyelia, anencephaly and spina bifida. Cerebrospinal Fluid Res 5:7PubMedCrossRef Williams H (2008) A unifying hypothesis for hydrocephalus, Chiari malformation, syringomyelia, anencephaly and spina bifida. Cerebrospinal Fluid Res 5:7PubMedCrossRef
67.
Zurück zum Zitat Zampino G, Pantaleoni F, Carta C, Cobellis G, Vasta I, Neri C, Pogna EA, DeFeo E, Delogu A, Sarlozy A, Atzeri F, Selicorni A, Rauen KA, Cytrymbaum CS, Weksberg R, Dallapiccola B, Ballabio A, Gelb BD, Neri G, Tartaglia M (2007) Diveristy, parental germline origin, and phenotypic spectrum of de novo HRAS missense changes in Costello syndrome. Hum Mutat 28(3):265–272PubMedCrossRef Zampino G, Pantaleoni F, Carta C, Cobellis G, Vasta I, Neri C, Pogna EA, DeFeo E, Delogu A, Sarlozy A, Atzeri F, Selicorni A, Rauen KA, Cytrymbaum CS, Weksberg R, Dallapiccola B, Ballabio A, Gelb BD, Neri G, Tartaglia M (2007) Diveristy, parental germline origin, and phenotypic spectrum of de novo HRAS missense changes in Costello syndrome. Hum Mutat 28(3):265–272PubMedCrossRef
Metadaten
Titel
Hydrocephalus and Chiari type I malformation
verfasst von
Concezio Di Rocco
Paolo Frassanito
Luca Massimi
Simone Peraio
Publikationsdatum
01.10.2011
Verlag
Springer-Verlag
Erschienen in
Child's Nervous System / Ausgabe 10/2011
Print ISSN: 0256-7040
Elektronische ISSN: 1433-0350
DOI
https://doi.org/10.1007/s00381-011-1545-3

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