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2014 | 73 | 2 |

Tytuł artykułu

Quantification of white matter fibre pathways disruption in frontal transcortical approach to the lateral ventricle or the interventricular foramen in diffusion tensor tractography

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EN

Abstrakty

EN
Pathologies occupying the interventricular foramen (foramen of Monro — FM) or the anterior part of lateral ventricle (LV) are accessed by the transcortical or transcallosal route. As severing of rostral corpus callosum has been deemed inferior to cortical incision, the approaches through various points of frontal lobe have been developed. Superior (F1), middle (F2) frontal gyrus or occasionally superior frontal sulcus are used as an entry of neurosurgical corridor. In spite of the fact that every approach to LV or FM causes its characteristic irreversible damage to white matter, to date all of transcortical routes are regarded as equivalent. The current study compared the damage of main neural bundles between virtual trans-F1 and trans-F2 corridors by means of diffusion tensor tractography method (DTT) in 11 magnetic resonance imaging (MRI) exams from clinical series (22 hemispheres, regardless of dominance). Corpus callosum, cingulum, subdivisions I and II of superior longitudinal fasciculus (SLF I and SLF II), corticoreticular as well as pyramidal tracts crossing both approaches were subjected to surgical violation. Both approaches served a similar total number of fibres (0.94 to 1.78 [× 10³]). Trans-F1 route caused significantly greater damage of total white matter volume (F1: 8.26 vs. F2: 7.16 mL), percentage of SLF I fibres (F1: 78.6% vs. F2: 28.6%) and cingulum (F1: 49.4% vs. F2: 10.6%), whereas trans-F2 route interrupted more corticoreticular fibres (F1: 4.5% vs. F2: 30.7%). Pyramidal tract (F1: 0.6% vs. F2: 1.3%) and SLF II (F1: 15.9% vs. F2: 26.2%) were marginally more vulnerable in case of the access via middle frontal gyrus. Both approaches destroyed 7% of callosal fibres. Summarising the above DTT findings, trans-F2 route disrupted a greater number of fibres from eloquent neural bundles (SLF II, pyramidal and corticoreticular tracts), therefore is regarded as inferior to trans-F1 one. Due to lack of up-to-date guidelines with recommendations of the approaches to LV or FM, an individual preoperative planning based on DTT should precede a surgery. (Folia Morphol 2014; 73, 2: 129–138)

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-

Czasopismo

Rocznik

Tom

73

Numer

2

Opis fizyczny

p.129-138,fig.,ref.

Twórcy

autor
  • Neurosurgery Department, Medical University of Gdansk, Gdansk, Poland
  • Neurosurgery Department, Medical University of Gdansk, Gdansk, Poland
autor
  • Neurosurgery Department, Medical University of Gdansk, Gdansk, Poland
autor
  • Neurosurgery Department, Medical University of Gdansk, Gdansk, Poland
  • Department of Maxillofacial and Oral Surgery, Medical University of Gdansk, Gdansk, Poland

Bibliografia

  • 1. Abe O, Masutani Y, Aoki S, Yamasue H, Yamada H, Kasai K, Mori H, Hayashi N, Masumoto T, Ohtomo K (2004) Topography of the human corpus callosum using diffusion tensor tractography. J Comput Assist Tomogr, 28: 533–539.
  • 2. Aicardi J (2008) Epilepsy syndromes. In: Engel J, Pedley T eds. Epilepsy: a comprehensive textbook. Lippincott Williams & Wilkins, New York, pp. 2283–2695.
  • 3. Antunes JL, Louis KM, Ganti SR (1980) Colloid cysts of the third ventricle. Neurosurgery, 7: 450–455.
  • 4. Apuzzo ML (1988) Surgery of masses affecting the third ventricular chamber: techniques and strategies. Clin Neurosurg, 34: 499–522.
  • 5. Aryan HE, Ozgur BM, Jandial R, Levy ML (2006) Complications of interhemispheric transcallosal approach in children: review of 15 years experience. Clin Neurol Neurosurg, 108: 790–793.
  • 6. Asgari S, Engelhorn T, Brondics A, Sandalcioglu IE, Stolke D (2003) ‘Transcortical or transcallosal approach to ventricle-associated lesions: a clinical study on the prognostic role of surgical approach. Neurosurg Rev, 26: 192–197.
  • 7. Basser PJ, Mattiello J, LeBihan D (1994) Estimation of the effective self-diffusion tensor from the NMR spin echo. J Magn Reson B, 103: 247–254.
  • 8. Basser PJ, Mattiello J, LeBihan D (1994) MR diffusion tensor spectroscopy and imaging. Biophys J, 66: 259–267.
  • 9. Basser PJ, Pajevic S, Pierpaoli C, Duda J, Aldroubi A (2000) In vivo fiber tractography using DT-MRI data. Magn Reson Med, 44: 625–632.
  • 10. Beaulieu C (2002) The basis of anisotropic water diffusion in the nervous system: a technical review. NMR Biomed, 15: 435–455.
  • 11. Broggi G (2008) Pain and psycho-affective disorders. Neurosurgery, 62: 901–919 (discussion 919–920).
  • 12. Bull JG (2010) Diffusion imaging and tractography. In: The paediatric neurosurgical population. University College, London.
  • 13. Cairns H (1971) Who’s in charge here?. Lancet, 2: 318–319.
  • 14. Carrasco EM (2011) Left intraventricular tumour resected via superior frontal transulcal transcortical approach. Neurosurgic blog and news channel. NEUROSURGIC.com, Santa Cruz, Bolivia.
  • 15. Casmiro M, Sintini M, Martinelli P, Leonardi M, D’alessandro R (1992) Chronic spastic atrophic hemiparesis with benign course. Ital J Neurol Sci, 13: 611–616.
  • 16. Catani M, Dell’acqua F, Vergani F, Malik F, Hodge H, Roy P, Valabregue R, Thiebaut De Schotten M (2012) Short frontal lobe connections of the human brain. Cortex, 48: 273–291.
  • 17. Catani M, Howard RJ, Pajevic S, Jones DK (2002) Virtual in vivo interactive dissection of white matter fasciculi in the human brain. Neuroimage, 17: 77–94.
  • 18. Ellenbogen RG (2001) Transcortical surgery for lateral ventricular tumors. Neurosurg Focus, 10: E2.
  • 19. Friedman MA, Meyers CA, Sawaya R (2003) Neuropsychological effects of third ventricle tumor surgery. Neurosurgery, 52: 791–798 (discussion 798).
  • 20. Fuh JL, Wang SJ (1995) Caudate hemorrhage: clinical features, neuropsychological assessments and radiological findings. Clin Neurol Neurosurg, 97: 296–299.
  • 21. Gasquoine PG (2013) Localization of function in anterior cingulate cortex: from psychosurgery to functional neuroimaging. Neurosci Biobehav Rev, 37: 340–348.
  • 22. Hasan KM, Kamali A, Iftikhar A, Kramer LA, Papanicolaou AC, Fletcher JM, Ewing-Cobbs L (2009) Diffusion tensor tractography quantification of the human corpus callosum fiber pathways across the lifespan. Brain Res, 1249: 91–100.
  • 23. Hassaneen W, Suki D, Salaskar AL, Levine NB, Demonte F, Lang FF, Mccutcheon IE, Dorai Z, Feiz-Erfan I, Wildrick DM, Sawaya R (2010) Immediate morbidity and mortality associated with transcallosal resection of tumors of the third ventricle. J Clin Neurosci, 17: 830–836.
  • 24. Hernesniemi J, Romani R, R. Dashti, Albayrak BS, Savolainen S, Ramsey C, Karatas A, Lehto H, Navratil O, Niemelä M (2008) Microsurgical treatment of third ventricular colloid cysts by interhemispheric far lateral transcallosal approach: experience of 134 patients. Surg Neurol, 69: 447–453 (discussion 453–446).
  • 25. Hoeft F, Barnea-Goraly N, Haas BW, Golarai G, Ng D, Mills D, Korenberg J, Bellugi U, Galaburda A, Reiss AL (2007) More is not always better: increased fractional anisotropy of superior longitudinal fasciculus associated with poor visuospatial abilities in Williams syndrome. J Neurosci, 27: 11960–11965.
  • 26. Ino T, Nakai R, Azuma T, Yamamoto T, Tsutsumi S, Fukuyama H (2007) Somatotopy of corticospinal tract in the internal capsule shown by functional MRI and diffusion tensor images. Neuroreport, 18: 665–668.
  • 27. Jang SH, Hong JH (2012) The anatomical characteristics of superior longitudinal fasciculus I in human brain: Diffusion tensor tractography study. Neurosci Lett, 506: 146–148.
  • 28. Jellison BJ, Field AS, Medow J, Lazar M, Salamat MS, Alexander AL (2004) Diffusion tensor imaging of cerebral white matter: a pictorial review of physics, fiber tract anatomy, and tumor imaging patterns. Am J Neuroradiol, 25: 356–369.
  • 29. Keedwell PA, Chapman R, Christiansen K, Richardson H, Evans J, Jones DK (2012) Cingulum white matter in young women at risk of depression: the effect of family history and anhedonia. Biol Psychiatry, 72: 296–302.
  • 30. LeBihan D, Mangin JF, Poupon C, Clark CA, Pappata S, Molko N, Chabriat H (2001) Diffusion tensor imaging: concepts and applications. J Magn Reson Imaging, 13: 534–546.
  • 31. Lin F, Yu C, Jiang T, Li K, Li X, Qin W, Sun H, Chan P (2006) Quantitative analysis along the pyramidal tract by length-normalized parameterization based on diffusion tensor tractography: application to patients with relapsing neuromyelitis optica. Neuroimage, 33: 154–160.
  • 32. Makris N, Kennedy DN, Mcinerney S, Sorensen AG, Wang R, Caviness VS, Pandya DN (2005) Segmentation of subcomponents within the superior longitudinal fascicle in humans: a quantitative, in vivo, DT-MRI study. Cereb Cortex, 15: 854–869.
  • 33. Matsuyama K, Mori F, Nakajima K, Drew T, Aoki M, Mori S (2004) Locomotor role of the corticoreticular-reticulospinal-spinal interneuronal system. Prog Brain Res, 143: 239–249.
  • 34. Milligan BD, Meyer FB (2010) Morbidity of transcallosal and transcortical approaches to lesions in and around the lateral and third ventricles: a single-institution experience. Neurosurgery, 67: 1483–1496 (discussion 1496).
  • 35. Morgane PJ, Galler JR, Mokler DJ (2005) A review of systems and networks of the limbic forebrain/limbic midbrain. Prog Neurobiol, 75: 143–160.
  • 36. Moore AJ, Newell DW (2005) Neurosurgery: principles and practice. Springer, London.
  • 37. Mukherjee P, Berman JI, Chung SW, Hess CP, Henry RG (2008) Diffusion tensor MR imaging and fiber tractography: theoretic underpinnings. Am J Neuroradiol, 29: 632–641.
  • 38. O’donnell L, Haker S, Westin C (2002) New approaches to estimation of white matter connectivity in diffusion tensor MRI: Elliptic PDE’s and geodesics in tensor-warped space. In: Proc. of Medical Image Computing and Computer-Assisted Intervention (MICCAI), Springer, Berlin Heidelberg, pp. 459–466.
  • 39. Park ES, Cho YH, Kim JH, Kim SJ, Khang SK, Kim CJ (2012) Frontal transcortical approach in 12 central neurocytomas. Acta Neurochir, 154: 1961–1971 (discussion 1972).
  • 40. Perneczky A, Reisch R (2008) Transcortical approach. Keyhole approaches in neurosurgery. Vol. 1: Concept and surgical technique. Springer-Verlag, Wien, pp. 267–282.
  • 41. Prince DA (1985) Physiological mechanisms of focal epileptogenesis. Epilepsia, 26 (suppl. 1): S3–S14.
  • 42. Qazi AA, Radmanesh A, O’donnell L, Kindlmann G, Peled S, Whalen S, Westin CF, Golby AJ (2009) Resolving crossings in the corticospinal tract by two-tensor streamline tractography: Method and clinical assessment using fMRI. Neuroimage, 47: Suppl 2 T98–106.
  • 43. Raj A, Kuceyeski A, Weiner M (2012) A network diffusion model of disease progression in dementia. Neuron, 73: 1204–1215.
  • 44. Shinoura N, Onodera T, Kurokawa K, Tsukada M, Yamada R, Tabei Y, Koizumi T, Yagi K (2010) Damage to the upper portion of area 19 and the deep white matter in the left inferior parietal lobe, including the superior longitudinal fasciculus, results in alexia with agraphia. Eur Neurol, 64: 224–229.
  • 45. Shinoura N, Suzuki Y, Yamada R, Tabei Y, Saito K, Yagi K (2009) Damage to the right superior longitudinal fasciculus in the inferior parietal lobe plays a role in spatial neglect. Neuropsychologia, 47: 2600–2603.
  • 46. Spooner J, Yu H, Kao C, Sillay K, Konrad P (2007) Neuromodulation of the cingulum for neuropathic pain after spinal cord injury. Case report. J Neurosurg, 107: 169–172.
  • 47. Sullivan EV, Adalsteinsson E, Pfefferbaum A (2006) Selective age-related degradation of anterior callosal fiber bundles quantified in vivo with fiber tracking. Cereb Cortex, 16: 1030–1039.
  • 48. Vigneron LM, Warfield SK, Robe PA, Verly JG (2011) 3D XFEM-based modeling of retraction for preoperative image update. Comput Aided Surg, 16: 121–134.
  • 49. Villani R, Tomei G (2006) Approach to tumors of the third ventricle. In: Schmidek H, Roberts D eds. Schmidek and Sweet’s operative neurosurgical techniques: indications, methods, and results. Saunders Elsevier, Philadelphia, pp. 772–785.
  • 50. Wen HT, Mussi ACM, Rhoton AL Jr., Oliveira ED, Tedeschi H (2006) Surgical approaches to lesions located in the lateral, third, and fourth ventricles. In: Sekhar LN, Fessler RG eds. Atlas of neurosurgical techniques: brain. Thieme, New York, pp. 527–528.
  • 51. Westerhausen R, Huster RJ, Kreuder F, Wittling W, Schweiger E (2007) Corticospinal tract asymmetries at the level of the internal capsule: is there an association with handedness? Neuroimage, 37: 379–386.
  • 52. Winn HR (2011) Youmans neurological surgery. Elsevier Saunders, Philadelphia.
  • 53. Yaşargil MG, Abdulrauf SI (2008) Surgery of intraventricular tumors. Neurosurgery, 62: 1029–1040 (discussion 1040–1021).
  • 54. Yeo SS, Chang MC, Kwon YH, Jung YJ, Jang SH (2012) Corticoreticular pathway in the human brain: diffusion tensor tractography study. Neurosci Lett, 508: 9–12.
  • 55. Yonekawa T, Nakagawa E, Takeshita E, Inoue Y, Inagaki M, Kaga M, Sugai K, Sasaki M, Kaido T, Takahashi A, Otsuki T (2011) Effect of corpus callosotomy on attention deficit and behavioral problems in pediatric patients with intractable epilepsy. Epilepsy Behav, 22: 697–704.
  • 56. Yu CS, Li KC, Xuan Y, Ji XM, Qin W (2005) Diffusion tensor tractography in patients with cerebral tumors: a helpful technique for neurosurgical planning and postoperative assessment. Eur J Radiol, 56: 197–204.
  • 57. Zhao Y, Chen X, Wang F, Sun G, Wang Y, Song Z, Xu B (2012) Integration of diffusion tensor-based arcuate fasciculus fibre navigation and intraoperative MRI into glioma surgery. J Clin Neurosci, 19: 255–261.

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Bibliografia

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