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Published in: Child's Nervous System 5/2017

01-05-2017 | Original Paper

Altered cerebrospinal fluid dynamics in neurofibromatosis type l: severe arachnoid thickening in patients with neurofibromatosis type 1 may cause abnormal CSF dynamic

Authors: Young Sill Kang, Eun-Kyung Park, Yong-Oock Kim, Ju-Seong Kim, Dong-Seok Kim, U. W. Thomale, Kyu-Won Shim

Published in: Child's Nervous System | Issue 5/2017

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Abstract

Introduction

The object of this study is to understand abnormal dynamic of cerebrospinal fluid (CSF) in patients with neurofibromatosis type 1 (NF1), which may cause temporal lobe herniation and bulging of temporal fossa.

Methods

Four patients, three females and one male, with NF1 were studied retrospectively. They presented with a similar craniofacial deformity, which consisted of pulsatile exophthalmos, an enlarged bony orbit, dysplasia of the sphenoid wing with the presence of a herniation of the temporal lobe into the orbit, and a bulging temporal fossa.

Results and discussion

Surgical exploration demonstrated abnormally thickened arachnoid membrane in one case. Protruding temporal lobe, which was one of the main symptoms in NF1 patients, could be stopped by control of intracranial pressure (ICP) via programmable ventriculoperitoneal shunt (VPS) or extra ventricle drainage implantation. The dense fibrosis of the arachnoid membrane and consequent altered hemispheric CSF dynamics may cause symptoms including pulsatile exophthalmos and consequent worsening of vision, prolapse of the temporal lobe, and enlargement of the temporal fossa. This finding may not present with general features of hydrocephalus, so that delays in diagnosis often result.

Conclusion

For the NF1 patients with cranio-orbito-temporal deformities, prior to any surgical reconstruction, control of increased ICP (IICP) should be primarily considered.
Literature
1.
go back to reference Gerber PA, Antal AS, Neumann NJ, Homey B, Matuschek C, Peiper M, Budach W, Bolke E (2009) Neurofibromatosis. Eur J Med Res 14:102–105PubMedPubMedCentral Gerber PA, Antal AS, Neumann NJ, Homey B, Matuschek C, Peiper M, Budach W, Bolke E (2009) Neurofibromatosis. Eur J Med Res 14:102–105PubMedPubMedCentral
2.
go back to reference Binet EF, Kieffer SA, Martin SH, Peterson HO (1969) Orbital dysplasia in neurofibromatosis. Radiology 93:829–833CrossRefPubMed Binet EF, Kieffer SA, Martin SH, Peterson HO (1969) Orbital dysplasia in neurofibromatosis. Radiology 93:829–833CrossRefPubMed
3.
go back to reference Mortada A (1967) Intermittent and pulsating exophthalmos. Bull Ophthalmol Soc Egypt 60:365–377PubMed Mortada A (1967) Intermittent and pulsating exophthalmos. Bull Ophthalmol Soc Egypt 60:365–377PubMed
5.
go back to reference Macfarlane R, Levin AV, Weksberg R, Blaser S, Rutka JT (1995) Absence of the greater sphenoid wing in neurofibromatosis type I: congenital or acquired: case report. Neurosurgery 37:129–133CrossRefPubMed Macfarlane R, Levin AV, Weksberg R, Blaser S, Rutka JT (1995) Absence of the greater sphenoid wing in neurofibromatosis type I: congenital or acquired: case report. Neurosurgery 37:129–133CrossRefPubMed
6.
go back to reference Marchac D (1984) Intracranial enlargement of the orbital cavity and palpebral remodeling for orbitopalpebral neurofibromatosis. Plast Reconstr Surg 73:534–543CrossRefPubMed Marchac D (1984) Intracranial enlargement of the orbital cavity and palpebral remodeling for orbitopalpebral neurofibromatosis. Plast Reconstr Surg 73:534–543CrossRefPubMed
7.
go back to reference Pomeranz SJ, Shelton JJ, Tobias J, Soila K, Altman D, Viamonte M (1987) MR of visual pathways in patients with neurofibromatosis. AJNR Am J Neuroradiol 8:831–836PubMed Pomeranz SJ, Shelton JJ, Tobias J, Soila K, Altman D, Viamonte M (1987) MR of visual pathways in patients with neurofibromatosis. AJNR Am J Neuroradiol 8:831–836PubMed
8.
go back to reference Krastinova-Lolov D, Hamza F (1996) The surgical management of cranio-orbital neurofibromatosis. Ann Plast Surg 36:263–269CrossRefPubMed Krastinova-Lolov D, Hamza F (1996) The surgical management of cranio-orbital neurofibromatosis. Ann Plast Surg 36:263–269CrossRefPubMed
9.
go back to reference Viskochil D, Buchberg AM, Xu G, Cawthon RM, Stevens J, Wolff RK, Culver M, Carey JC, Copeland NG, Jenkins NA et al (1990) Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus. Cell 62:187–192CrossRefPubMed Viskochil D, Buchberg AM, Xu G, Cawthon RM, Stevens J, Wolff RK, Culver M, Carey JC, Copeland NG, Jenkins NA et al (1990) Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus. Cell 62:187–192CrossRefPubMed
10.
go back to reference Cawthon RM, Weiss R, Xu GF, Viskochil D, Culver M, Stevens J, Robertson M, Dunn D, Gesteland R, O’Connell P et al (1990) A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations. Cell 62:193–201CrossRefPubMed Cawthon RM, Weiss R, Xu GF, Viskochil D, Culver M, Stevens J, Robertson M, Dunn D, Gesteland R, O’Connell P et al (1990) A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations. Cell 62:193–201CrossRefPubMed
11.
go back to reference Wallace MR, Marchuk DA, Andersen LB, Letcher R, Odeh HM, Saulino AM, Fountain JW, Brereton A, Nicholson J, Mitchell AL et al (1990) Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients. Science 249:181–186CrossRefPubMed Wallace MR, Marchuk DA, Andersen LB, Letcher R, Odeh HM, Saulino AM, Fountain JW, Brereton A, Nicholson J, Mitchell AL et al (1990) Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients. Science 249:181–186CrossRefPubMed
12.
go back to reference Abdel-Wanis ME, Kawahara N (2002) The role of neurofibromin and melatonin in pathogenesis of pseudarthrosis after spinal fusion for neurofibromatous scoliosis. Med Hypotheses 58:395–398CrossRefPubMed Abdel-Wanis ME, Kawahara N (2002) The role of neurofibromin and melatonin in pathogenesis of pseudarthrosis after spinal fusion for neurofibromatous scoliosis. Med Hypotheses 58:395–398CrossRefPubMed
13.
go back to reference Drobnik J, Dabrowski R (1996) Melatonin suppresses the pinealectomy-induced elevation of collagen content in a wound. Cytobios 85:51–58PubMed Drobnik J, Dabrowski R (1996) Melatonin suppresses the pinealectomy-induced elevation of collagen content in a wound. Cytobios 85:51–58PubMed
14.
go back to reference Friedrich RE, Heiland M, Kehler U, Schmelzle R (2003) Reconstruction of sphenoid wing dysplasia with pulsating exophthalmos in a case of neurofibromatosis type 1 supported by intraoperative navigation using a new skull reference system. Skull Base 13:211–217CrossRefPubMedPubMedCentral Friedrich RE, Heiland M, Kehler U, Schmelzle R (2003) Reconstruction of sphenoid wing dysplasia with pulsating exophthalmos in a case of neurofibromatosis type 1 supported by intraoperative navigation using a new skull reference system. Skull Base 13:211–217CrossRefPubMedPubMedCentral
15.
go back to reference Alwan S, Armstrong L, Joe H, Birch PH, Szudek J, Friedman JM (2007) Associations of osseous abnormalities in neurofibromatosis 1. Am J Med Genet A 143A:1326–1333CrossRefPubMed Alwan S, Armstrong L, Joe H, Birch PH, Szudek J, Friedman JM (2007) Associations of osseous abnormalities in neurofibromatosis 1. Am J Med Genet A 143A:1326–1333CrossRefPubMed
16.
go back to reference Jacquemin C, Bosley TM, Svedberg H (2003) Orbit deformities in craniofacial neurofibromatosis type 1. AJNR Am J Neuroradiol 24:1678–1682PubMed Jacquemin C, Bosley TM, Svedberg H (2003) Orbit deformities in craniofacial neurofibromatosis type 1. AJNR Am J Neuroradiol 24:1678–1682PubMed
17.
go back to reference Hunt JC, Pugh DG (1961) Skeletal lesions in neurofibromatosis. Radiology 1–20 Hunt JC, Pugh DG (1961) Skeletal lesions in neurofibromatosis. Radiology 1–20
18.
go back to reference Anderson FM, Segall HD, Caton WL (1979) Use of computerized tomography scanning in supratentorial arachnoid cysts. A report on 20 children and four adults. J Neurosurg 50:333–338CrossRefPubMed Anderson FM, Segall HD, Caton WL (1979) Use of computerized tomography scanning in supratentorial arachnoid cysts. A report on 20 children and four adults. J Neurosurg 50:333–338CrossRefPubMed
19.
go back to reference Leo JS, Pinto RS, Hulvat GF, Epstein F, Kricheff II (1979) Computed tomography of arachnoid cysts. Radiology 130:675–680CrossRefPubMed Leo JS, Pinto RS, Hulvat GF, Epstein F, Kricheff II (1979) Computed tomography of arachnoid cysts. Radiology 130:675–680CrossRefPubMed
20.
go back to reference Smith RA, Smith WA (1976) Arachnoid cysts of the middle cranial fossa. Surg Neurol 5:246–254PubMed Smith RA, Smith WA (1976) Arachnoid cysts of the middle cranial fossa. Surg Neurol 5:246–254PubMed
21.
go back to reference Wilkins RH, Radtka RA, Burger PC (1993) Spontaneous temporal encephalocele. J Nerosurg 78:492–498CrossRef Wilkins RH, Radtka RA, Burger PC (1993) Spontaneous temporal encephalocele. J Nerosurg 78:492–498CrossRef
22.
go back to reference Rilliet B, Pittet B, Montandon D, Narata AP, de Ribaupierre S, Schils F, Boscherini D, Di Rocco C, Ducrey N (2010) Orbitotemporal facial involvement in type 1 neurofibromatosis (NF1). Neurochirurgie 56:257–270CrossRefPubMed Rilliet B, Pittet B, Montandon D, Narata AP, de Ribaupierre S, Schils F, Boscherini D, Di Rocco C, Ducrey N (2010) Orbitotemporal facial involvement in type 1 neurofibromatosis (NF1). Neurochirurgie 56:257–270CrossRefPubMed
23.
go back to reference Huson SM, Harper PS, Compston DA (1988) Von Recklinghausen neurofibromatosis: clinical and population study in South East Wales. Brain 55–81 Huson SM, Harper PS, Compston DA (1988) Von Recklinghausen neurofibromatosis: clinical and population study in South East Wales. Brain 55–81
24.
go back to reference Afifi AK, Dolan KD, Van Gilder JC, Fincham RW (1988) Ventriculomegaly in neurofibromatosis-1. Association with Chiari type I malformation. Neurofibromatosis 1:299–305PubMed Afifi AK, Dolan KD, Van Gilder JC, Fincham RW (1988) Ventriculomegaly in neurofibromatosis-1. Association with Chiari type I malformation. Neurofibromatosis 1:299–305PubMed
25.
go back to reference Bognanno JR, Edwards MK, Lee TA, Dunn DW, Roos KL, Klatte EC (1988) Cranial MR imaging in neurofibromatosis. AJNR 9:461–468 Bognanno JR, Edwards MK, Lee TA, Dunn DW, Roos KL, Klatte EC (1988) Cranial MR imaging in neurofibromatosis. AJNR 9:461–468
26.
go back to reference Dandy WE (1929) An operative treatment for certain cases of meningocele (or encephalocele) into the orbit. Arch Ophthalmol 2:123–132CrossRef Dandy WE (1929) An operative treatment for certain cases of meningocele (or encephalocele) into the orbit. Arch Ophthalmol 2:123–132CrossRef
27.
go back to reference Lotfy M, Xu R, McGirt M, Sakr S, Ayoub B, Bydon A (2010) Reconstruction of skull base defects in sphenoid wing dysplasia associated with neurofibromatosis I with titanium mesh. Clin Neurol Neurosurg 112:909–914CrossRefPubMed Lotfy M, Xu R, McGirt M, Sakr S, Ayoub B, Bydon A (2010) Reconstruction of skull base defects in sphenoid wing dysplasia associated with neurofibromatosis I with titanium mesh. Clin Neurol Neurosurg 112:909–914CrossRefPubMed
Metadata
Title
Altered cerebrospinal fluid dynamics in neurofibromatosis type l: severe arachnoid thickening in patients with neurofibromatosis type 1 may cause abnormal CSF dynamic
Authors
Young Sill Kang
Eun-Kyung Park
Yong-Oock Kim
Ju-Seong Kim
Dong-Seok Kim
U. W. Thomale
Kyu-Won Shim
Publication date
01-05-2017
Publisher
Springer Berlin Heidelberg
Published in
Child's Nervous System / Issue 5/2017
Print ISSN: 0256-7040
Electronic ISSN: 1433-0350
DOI
https://doi.org/10.1007/s00381-017-3370-9

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