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Hydrozephalus und Liquorzirkulationsstörungen

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Zusammenfassung

Nach einer Darstellung der Anatomie des Plexus choroideus und der Physiologie des Liquor cerebrospinalis werden Pathologie und Pathogenese des nicht-kommunizierenden, kommunizierenden und hypersekretorischen Hydrozephalus besprochen.

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Literatur

  1. Azzi GM, Canady AI, Ham S, Mitchell JA (1999) Kaolininduced hydrocephalus in the hamster: temporal sequence of changes in intracranial pressure, ventriculomegaly and whole-brain specific gravity. Acta Neuropathol 98: 245–250

    Article  PubMed  CAS  Google Scholar 

  2. Britz GW, Kim DK, Loeser JD (1996) Hydrocephalus secondary to diffuse villous hyperplasia of the choroid plexus. Case report and review of the literature. J Neurosurg 85: 689–691

    Article  PubMed  CAS  Google Scholar 

  3. Brunetti-Pierri N, Berg JS, Scaglia F et al. (2008) Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities. Nat Genet 40: 1466–1471

    Article  PubMed  CAS  Google Scholar 

  4. Bruni JE, Del Bigio MR, Cardoso ER, Persaud TVN (1988) Hereditary hydrocephalus in laboratory animals and humans. Exp Pathol 35: 239–246

    PubMed  CAS  Google Scholar 

  5. Buttner A, Winkler PA, Eisenmenger W, Weis S (1997) Colloid cysts of the third ventricle with fatal outcome: a report of two cases and review of the literature. Int J Legal Med 110: 260–266

    Article  PubMed  CAS  Google Scholar 

  6. Chalmers RM, Andreae L, Wood NW, Durai Raj RV, Casey AT (1999) Familial hydrocephalus. J Neurol Neurosurg Psychiatry 67: 410–411

    Article  PubMed  CAS  Google Scholar 

  7. Campeau PM, Ah Mew N, Cartier L, Mackay KL, Shaffer LG, Der Kaloustian VM, Thomas MA (2008) Prenatal diagnosis of monosomy 1p36: a focus on brain abnormalities and a review of the literature. Am J Med Genet 146A: 3062–3069

    Article  PubMed  Google Scholar 

  8. Choux M, Di Rocco C, Hockley AD, Walker ML (1999) Pediatric Neurosurgery. Churchill Livingstone, London

    Google Scholar 

  9. Cinalli G (1999) Alternatives to shunting. Child’s Nerv Syst 15: 718–731

    Article  CAS  Google Scholar 

  10. Corkill RG, Cadoux-Hudsen TAD (1999) Normal pressure hydrocephalus: developments in determining surgical prognosis. Curr Opin Neurol 12: 671–677

    Article  PubMed  CAS  Google Scholar 

  11. Crews L, Wyss-Coray T, Masliah E (2004) Insights into the pathogenesis of hydrocephalus from transgenic and experimental animal models. Brain Pathol 14: 312–316

    Article  PubMed  CAS  Google Scholar 

  12. Criscuolo GR, Symon L (1986) Intraventricular meningioma. A review of 10 cases of the National Hospital, Queen Square (1974–1985) with reference to the literature. Acta Neurochir 83: 83–91

    Article  CAS  Google Scholar 

  13. Dandy WE, Blackfan KD (1914) Internal hydrocephalus. An experimental, clinical and pathological study. Am J Dis Child 8: 406–482

    Google Scholar 

  14. Davy BE, Robinson ML (2003) Congenital hydrocephalus in hy3 mice is caused by a frameshift mutation in Hydin, a large novel gene. Hum Mol Genet 12: 1163–1170

    Article  PubMed  CAS  Google Scholar 

  15. Del Bigio MR (1993) Neuropathological changes caused by hydrocephalus. Acta Neuropathol 85: 573–585

    Article  PubMed  Google Scholar 

  16. Ellison D, Love S, Chimelli L, Harding BN, Lowe J, Vinters HV (2004) Hydrocephalus. Neuropathology – A reference text of CNS pathology, 2. Aufl. Mosby, Edinburgh, pp 111–118

    Google Scholar 

  17. Esiri MM (1996) Hydrocephalus, cysts and syrinxes. Oppenheimer’s Diagnostic Neuropathology, 2. Aufl. Blackwell Science, Oxford, pp 142–151

    Google Scholar 

  18. Friede RL (1989) Developmental neuropathology, 2. Aufl. Springer, Berlin, pp 220–246

    Google Scholar 

  19. Gilkes CE, Steers AJW, Minns RA (2000) CSF shunt malfunction: a study of the spectrum of mechanisms and clinical presentation. Child’s Nerv Syst 16: 122

    Article  Google Scholar 

  20. Gjerris F, Børgesen SE (2000) Pathophysiology of cerebrospinal fluid circulation. In: Crockard A, Hayward R, Hoff JT (eds) Neurosurgery – the scientific basis of clinical practice. Blackwell Science, London, pp 147–168

    Google Scholar 

  21. Goto J, Tezuka T, Nakazawa T, Sagara H, Yamamoto T (2008) Loss of Fyn tyrosine kinase on the C57BL/6 genetic background causes hydrocephalus with defects in oligodendrocyte development. Mol Cell Neurosci 38: 203–212

    Article  PubMed  CAS  Google Scholar 

  22. Graff-Radford NR, Torner J, Adams HP, Kassell NF (1989) Factors associated with hydrocephalus after subarachnoid hemorrhage. Arch Neurol 46: 744–752

    PubMed  CAS  Google Scholar 

  23. Hagberg G, Fernell E, von Wendt L (1988) Epidemiology of infantile hydrocephalus in Sweden. Reduced optimality in prepartum, partum and postpartum conditions. A casecontrol study. Neuropediatr 19: 16–23

    Article  CAS  Google Scholar 

  24. Hakim S, Adams RD (1965) The special clinical problem of symptomatic hydrocephalus with normal cerebrospinal fluid pressure. Observations on cerebrospinal fluid hydrodynamics. J Neurol Sci 2: 307–327

    Article  PubMed  CAS  Google Scholar 

  25. Hakim S, Venegas JG, Burton JD (1976) The physics of the cranial cavity, hydrocephalus and normal pressure hydrocephalus: mechanical interpretation and mathematical model. Surg Neurol 5: 187–210

    PubMed  CAS  Google Scholar 

  26. Haverkamp F, Wölfle J, Aretz M, Krämer A, Höhmann B, Fahnenstich H, Zerres K (1999) Congenital hydrocephalus internus and aqueduct stenosis: aetiology and implications for genetic counselling. Eur J Pediatr 158: 474–478

    Article  PubMed  CAS  Google Scholar 

  27. Hochwald GM (1985) Animal models of hydrocephalus: recent developments. Proc Soc Exp Biol Med 178: 1–11

    PubMed  CAS  Google Scholar 

  28. Hoppe-Hirsch E, Laroussinie F, Brunet L, Sainte-Rose C, Renier D, Cinalli G, Zerah M, Pierre-Kahn A (1998) Late outcome of the surgical treatment of hydrocephalus. Child’s Nerv Syst 14: 97–99

    Article  CAS  Google Scholar 

  29. Jeng LB, Tarvin R, Robin NH (2001) Genetic advances in central nervous system malformations in the fetus and neonate. Semin Pediatr Neurol 8: 89–99

    Article  PubMed  CAS  Google Scholar 

  30. Jouet M, Rosenthal A, MacFarlane JA, Kenwrick S, Donnai D (1993) A missense mutation confirms the L1 defect in X-linked hydrocephalus. Nature Genet 4: 331

    Article  PubMed  CAS  Google Scholar 

  31. Kakita A, Takahashi H (2004) Hydrocephalus. In: Golden JA, Harding BN (eds) Pathology & Genetics. Developmental Neuropathology. ISN Neuropath Press, Basel, pp 126–130

    Google Scholar 

  32. Kang JK, Lee IW (1999) Long-term follow-up of shunting therapy. Child’s Nerv Syst 15: 711–771

    Article  CAS  Google Scholar 

  33. Katsuragi S, Teraoka K, Ikegami K, Amano K, Yamashita K, Ishizuka K, Miyakawa T (2000) Late onset X-linked hydrocephalus with normal cerebrospinal fluid pressure. Psychiatry Clin Neurosci 5: 487–492

    Article  Google Scholar 

  34. Keene DL, Ventureyra ECG (1999) Hydrocephalus and epileptic seizures. Child’s Nerv Syst 15: 158–162

    Article  CAS  Google Scholar 

  35. Leestma JE (1988) Forensic Neuropathology. Raven Press, New York

    Google Scholar 

  36. McComb JG, Davis RL (1991) Choroid plexus, cerebrospinal fluid, hydrocephalus, cerebral edema, and herniation phenomena. In: Davis RL, Robertson DM (eds) Textbook of Neuropathology, 2nd edn. Williams & Wilkins, Baltimore, pp 175–187

    Google Scholar 

  37. Milhorat TH (1996) Hydrocephalus: Pathophysiology and clinical features. In: Wilkins RH, Rengachary SS (eds) Neurosurgery, 2nd edn. McGraw-Hill, New York, pp 3625–3631

    Google Scholar 

  38. Milhorat TH, Hammock MK, Davis DA, Fenstermacher JD (1976) Choroid plexus papilloma. I. Proof of cerebrospinal fluid overproduction. Child’s Brain 2: 273–289

    PubMed  CAS  Google Scholar 

  39. Mori K (1995) Current concept of hydrocephalus: evolution of new classifications. Child’s Nerv Syst 11: 523–532

    Article  CAS  Google Scholar 

  40. Nakakimura S, Sasaki F, Okada T, Arisue A, Cho K, Yoshino M, Kanemura Y, Yamasaki M, Todo S (2008) Hirschsprung’s disease, acrocallosal syndrome, and congenital hydrocephalus: report of 2 patients and literature review. J Pediatr Surg 43: E13–17

    Article  PubMed  Google Scholar 

  41. Norman MG, McGillivray BC, Kalousek DK, Hill A, Poskitt KJ (1995) Congenital malformations of the brain. Oxford University Press, New York, pp 333–339

    Google Scholar 

  42. Oi S, Yamada H, Sato O, Matsumoto S (1996) Experimental models of congenital hydrocephalus and comparable clinical problems in the fetal and neonatal periods. Child’s Nerv Syst 12: 292–302

    Article  CAS  Google Scholar 

  43. Okamoto N, Del Maestro R, Valero R, Monros E, Poo P, Kanemura Y, Yamasaki M (2004) Hydrocephalus and Hirschsprung’s disease with a mutation of L1CAM. J Hum Genet 49: 334–337

    Article  PubMed  Google Scholar 

  44. Piatt JH, Carlson CV (1996) Hydrocephalus and epilepsy: an actuarial analysis. Neurosurgery 39: 722–728

    Article  PubMed  Google Scholar 

  45. Portenoy RK, Berger A, Gross E (1984) Familial occurrence of idiopathic normal-pressure hydrocephalus. Arch Neurol 41: 335–337

    PubMed  CAS  Google Scholar 

  46. Portnoy HD, Branch C, Castro ME (1994) The relationship of intracranial venous pressure to hydrocephalus. Child’s Nerv Syst 10: 29–35

    Article  CAS  Google Scholar 

  47. Richards HK, Kane CO, Seeley H, Madakbas M, Whitfield P, Pickard JD (2000) The U.K. Shunt Registry. Child’s Nerv Syst 16: 123

    Google Scholar 

  48. Rickert CH (1998) Abdominal metastases of pediatric brain tumors via ventriculo-peritoneal shunts. Child‘s Nerv Syst 14: 10–14

    Article  CAS  Google Scholar 

  49. Rickert CH (1999) Neuropathology and prognosis of foetal brain tumours. Acta Neuropathol 98: 567–576

    Article  PubMed  CAS  Google Scholar 

  50. Rickert CH, Grabellus F, Varchmin-Schultheiß K, Stöß H, Paulus W (2001) Sudden unexpected death in young adults with chronic hydrocephalus. Int J Legal Med 114: 331–337

    Article  PubMed  CAS  Google Scholar 

  51. Robledo RF, Ciciotte SL, Gwynn B, Sahr KE, Gilligan DM, Mohandas N, Peters LL (2008) Targeted deletion of alphaadducin results in absent beta- and gamma-adducin, compensated hemolytic anemia, and lethal hydrocephalus in mice. Blood 112: 4298–4307

    Article  PubMed  CAS  Google Scholar 

  52. Rosenthal A, Jouet M, Kenwrick S (1992) Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X-linked hydrocephalus. Nature Genet 2: 107–112

    Article  PubMed  CAS  Google Scholar 

  53. Sabaratnam M (2000) Pathological and neuropathological findings in two males with fragile-X chromosome. J Intellect Disabil Res 44: 81–85

    Article  PubMed  Google Scholar 

  54. Saillour Y, Zanni G, Des Portes Vet al. (2007) Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal ganglia. J Med Genet 44: 739–744

    Article  PubMed  CAS  Google Scholar 

  55. Shaw CM, Alvord EC (1995) Hydrocephalus. In: Duckett S (ed) Pediatric neuropathology. Williams & Wilkins, Baltimore, pp 149–211

    Google Scholar 

  56. Schurr PH, Polkey CE (1993) Hydrocephalus. Oxford University Press, New York

    Google Scholar 

  57. Shen XQ, Miyajima M, Ogino I, Arai H (2006) Expression of the water-channel protein aquaporin 4 in the H-Tx rat: possible compensatory role in spontaneously arrested hydrocephalus. J Neurosurg 105: 459–464

    PubMed  Google Scholar 

  58. Sutton LN, Wood JH, Brooks BR, Barrer SJ, Kline M, Cohen SR (1983) Cerebrospinal fluid myelin basic protein in hydrocephalus. J Neurosurg 59: 467–470

    Article  PubMed  CAS  Google Scholar 

  59. Tegay DH, Lane AH, Roohi J, Hatchwell E (2007) Contiguous gene deletion involving L1CAM and AVPR2 causes X-linked hydrocephalus with nephrogenic diabetes insipidus. Am J Med Genet 143: 594–598

    Article  PubMed  Google Scholar 

  60. Töndury G, Kubik S, Krisch B (1987) Hirnhäute und Hirngefäße. In: Leonhardt H, Tillmann B, Töndury G, Zilles K (Hrsg) Anatomie des Menschen – Nervensystem, Sinnesorgane, 20. Aufl. Thieme, Stuttgart, S 186–191

    Google Scholar 

  61. Ulfig N, Bohl J, Neudörfer F, Rezaie P (2004) Brain macrophages and microglia in human fetal hydrocephalus. Brain Dev 26: 307–315

    Article  PubMed  Google Scholar 

  62. Vanneste JA (1994) Three decades of normal pressure hydrocephalus: are we wiser now? J Neurol Neurosurg Psychiatry 57: 1021–1025

    Article  PubMed  CAS  Google Scholar 

  63. Venes JL, Dauser RC (1987) Epilepsy following ventricular shunt placement. J Neurosurg 66: 154–155

    PubMed  CAS  Google Scholar 

  64. Vincent C, Kalatzis V, Compain S et al. (1994) A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR gene. Hum Mol Genet 3: 1859–1866

    Article  PubMed  CAS  Google Scholar 

  65. Vinters HV, Kleinschmidt-DeMasters BK (2008) Hydrocephalus: pathophysiology, causes and consequences for the central nervous system. In: Love S, Louis DN, Ellison DW (eds) Greenfield’s Neuropathology, 8th edn. Hodder Arnold, London, pp 52–56

    Google Scholar 

  66. Warkany J, Lemire RJ, Cohen MM (1981) Mental retardation and congenital malformations of the central nervous system. Year Book Medical Publishers, Chicago, pp 48–82

    Google Scholar 

  67. Weller RO, Kida S, Zhang ET (1992) Pathways of fluid drainage from the brain – morphological aspects and immunological significance in rat and man. Brain Pathol 2: 277–284

    Article  PubMed  CAS  Google Scholar 

  68. Wisniewski KE, Segan SM, Miezejeski CM, Sersen EA, Rudelli RD (1991) The Fra(X) syndrome: neurological, electrophysiological, and neuropathological abnormalities. Am J Med Genet 38: 476–480

    Article  PubMed  CAS  Google Scholar 

  69. Zhang J, Williams MA, Rigamonti D (2006) Genetics of human hydrocephalus. J Neurol 253: 1255–1266

    Article  PubMed  CAS  Google Scholar 

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Rickert, C. (2012). Hydrozephalus und Liquorzirkulationsstörungen. In: Klöppel, G., Kreipe, H., Remmele, W., Paulus, W., Schröder, J. (eds) Pathologie. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-02324-8_4

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  • DOI: https://doi.org/10.1007/978-3-642-02324-8_4

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