Laboratory Pathway Dissection from Medial Approach to Brain Hemisphere
Authors:
A. Hejčl 1–3; R. Bartoš 1,2; A. Zolal 1,2; A. Malucelli 1,2; M. Sameš 1,2; P. Petrovický 4
Authors place of work:
Neurochirurgická klinika UJEP a Krajská zdravotní, a. s. – Masarykova nemocnice v Ústí nad Labem
1; Neuroanatomická laboratoř UJEP v Ústí nad Labem
2; Centrum klinického výzkumu ICRC, Brno
3; Anatomický ústav 1. LF UK v Praze
4
Published in the journal:
Cesk Slov Neurol N 2012; 75/108(6): 707-713
Category:
Original Paper
Summary
In our paper we introduce the Klingler’s laboratory dissection of brain white matter tracts from the medial aspect of brain hemisphere. We continue in our previously published paper on white matter tracts dissection from the lateral aspect. Anatomical preparations are supplemented with tractographic imaging of some of the white matter tracts.
Key words:
white matter tracts – tractography – Klingler’s dissection
Zdroje
1. Bartoš R, Hejčl A, Zolal A, Malucelli A, Sameš M, Petrovický P. Laboratorní disekce drah laterálního aspektu mozkové hemisféry. Cesk Slov Neurol N 2012; 75/108(1): 30–37.
2. Agrawal A, Kapfhammer JP, Kress A, Wichers H, Deep A, Feindel W et al. Josef Klingler‘s models of white matter tracts: influences on neuroanatomy, neurosurgery, and neuroimaging. Neurosurgery 2011 69(2): 238–252.
3. Hong JH, Choi BY, Chang CH, Kim SH, Jung YJ, Byun WM et al. Injuries of cingulum and fornix following rupture of anterior communicating artery aneurysm: a diffusion tensor tractography study. Neurosurgery 2012; 70(4): 819–823.
4. Chang MC, Kim SH, Kim OL, Bai DS, Jang SH. The relation between fornix injury and memory impairment in patients with diffuse axonal injury: a diffusion tensor imaging study. NeuroRehabilitation 2010; 26(4): 347–353.
5. Chang MC, Jang SH. Corpus callosum injury in patients with diffuse axonal injury: a diffusion tensor imaging study. NeuroRehabilitation 2010; 26(4): 339–345.
6. Petrovický P. Anatomie s topografií a klinickými aplikacemi III. Martin: Osveta; 2001.
7. Petrovický P. Klinická neuroanatomie CNS. Praha//Kroměříž: Triton 2008.
8. von Lehe M, Wagner J, Wellmer J, Clusmann H, Kral T. Epilepsy surgery of the cingulate gyrus and the fronto-mesial cortex. Neurosurgery 2012; 70(4): 900–910.
9. von Lehe M, Schramm J. Gliomas of the cingulate gyrus: surgical management and functional outcome. Neurosurg Focus 2009; 27(2): E9.
10. Abdul-Rahman MF, Qiu A, Sim K. Regionally specific white matter disruptions of fornix and cingulum in schizophrenia. PLoS One 2011; 6(4): e18652.
11. O‘Dwyer L, Lamberton F, Bokde AL, Ewers M, Faluyi YO, Tanner C et al. Multiple indices of diffusion identifies white matter damage in mild cognitive impairment and Alzheimer‘s disease. PLoS One 2011; 6(6): e21745.
12. Kim JW, Lee DY, Choo IH, Seo EH, Kim SG, Park SY et al. Microstructural Alteration of the Anterior Cingulum is Associated With Apathy in Alzheimer Disease. Am J Geriatr Psychiatry 2011; 19(7): 644–653.
13. Yurgelun-Todd DA, Bueler CE, McGlade EC, Churchwell JC, Brenner LA, Lopez-Larson MP. Neuroimaging correlates of traumatic brain Injury and suicidal behavior. J Head Trauma Rehabil 2011; 26(4): 276–289.
14. Kim H, Piao Z, Liu P, Bingaman W, Diehl B. Secondary white matter degeneration of the corpus callosum in patients with intractable temporal lobe epilepsy: a diffusion tensor imaging study. Epilepsy Res 2008; 81(2–3): 136–142.
15. Witelson SF. Hand and sex differences in the isthmus and genu of the human corpus callosum. A postmortem morphological study. Brain 1989; 112 (Pt 3): 799–835.
16. Hofer S, Frahm J. Topography of the human corpus callosum revisited – comprehensive fiber tractography using diffusion tensor magnetic resonance imaging. Neuroimage 2006; 32(3): 989–994.
17. Wahl M, Lauterbach-Soon B, Hattingen E, Jung P, Singer O, Volz S et al. Human motor corpus callosum: topography, somatotopy, and link between microstructure and function. J Neurosci 2007; 27(45): 12132–12138.
18. Jea A, Vachhrajani S, Widjaja E, Nilsson D, Raybaud C, Shroff M et al. Corpus callosotomy in children and the disconnection syndromes: a review. Childs Nerv Syst 2008; 24(6): 685–692.
19. Kasowski H, Piepmeier JM. Transcallosal approach for tumors of the lateral and third ventricles. Neurosurg Focus 2001; 10(6): E3.
20. Peltier J, Verclytte S, Delmaire C, Deramond H, Pruvo JP, Le Gars D et al. Microsurgical anatomy of the ventral callosal radiations: new destination, correlations with diffusion tensor imaging fiber-tracking, and clinical relevance. J Neurosurg 2010; 112(3): 512–519.
21. Mosier K, Bereznaya I. Parallel cortical networks for volitional control of swallowing in humans. Exp Brain Res 2001; 140(3): 280–289.
22. Tettamanti M, Paulesu E, Scifo P, Maravita A, Fazio F, Perani D, et al. Interhemispheric transmission of visuomotor information in humans: fMRI evidence. J Neurophysiol 2002; 88(2): 1051–1058.
23. Mazerolle EL, D‘Arcy RC, Beyea SD. Detecting functional magnetic resonance imaging activation in white matter: interhemispheric transfer across the corpus callosum. BMC Neurosci 2008; 9: 84.
24. Mazerolle EL, Beyea SD, Gawryluk JR, Brewer KD, Bowen CV, D‘Arcy RC. Confirming white matter fMRI activation in the corpus callosum: co-localization with DTI tractography. Neuroimage 2010; 50(2): 616–621.
25. Gawryluk JR, D‘Arcy RC, Mazerolle EL, Brewer KD, Beyea SD. Functional mapping in the corpus callosum: a 4T fMRI study of white matter. Neuroimage 2011; 54(1): 10–15.
26. Horn EM, Feiz-Erfan I, Bristol RE, Lekovic GP, Goslar PW, Smith KA et al. Treatment options for third ventricular colloid cysts: comparison of open microsurgical versus endoscopic resection. Neurosurgery 2008; 62 (6 Suppl 3): 1076–1083.
27. Grondin RT, Hader W, MacRae ME, Hamilton MG. Endoscopic versus microsurgical resection of third ventricle colloid cysts. Can J Neurol Sci 2007; 34(2): 197–207.
28. Hong JH, Jang SH. Degeneration of cingulum and fornix in a patient with traumatic brain injury: diffuse tensor tractography study. J Rehabil Med 2010; 42(10) 979–981.
29. Hattori T, Sato R, Aoki S, Yuasa T, Mizusawa H. Different Patterns of Fornix Damage in Idiopathic Normal Pressure Hydrocephalus and Alzheimer Disease. AJNR Am J Neuroradiol 2012; 33(2); 274–279.
30. Colnat-Coulbois S, Mok K, Klein D, Penicaud S, Tanriverdi T, Olivier A. Tractography of the amygdala and hippocampus: anatomical study and application to selective amygdalohippocampectomy. J Neurosurg 2010; 113(6): 1135–1143.
31. Sincoff EH, Tan Y, Abdulrauf SI. White matter fiber dissection of the optic radiations of the temporal lobe and implications for surgical approaches to the temporal horn. J Neurosurg 2004; 101(5): 739–746.
32. Kawashima M, Li X, Rhoton AL jr, Ulm AJ, Oka H, Fujii K. Surgical approaches to the atrium of the lateral ventricle: microsurgical anatomy. Surg Neurol 2006; 65(5): 436–445.
33. Jacobson DM. The localizing value of a quadrantanopia. Arch Neurol 1997; 54(4): 401–404.
34. Marino R jr, Rasmussen T. Visual field changes after temporal lobectomy in man. Neurology 1968; 18(9): 825–835.
35. Pujari VB, Jimbo H, Dange N, Shah A, Singh S, Goel A. Fiber dissection of the visual pathways: analysis of the relationship of optic radiations to lateral ventricle: a cadaveric study. Neurol India 2008; 56(2): 133–137.
36. Tecoma ES, Laxer KD, Barbaro NM, Plant GT. Frequency and characteristics of visual field deficits after surgery for mesial temporal sclerosis. Neurology 1993; 43(6): 1235–1238.
37. Jensen I, Seedorff HH. Temporal lobe epilepsy and neuro-ophthalmology. Ophthalmological findings in 74 temporal lobe resected patients. Acta Ophthalmol (Copenh) 1976; 54(6): 827–841.
38. Ebeling U, Reulen HJ. Neurosurgical topography of the optic radiation in the temporal lobe. Acta Neurochir (Wien) 1988; 92(1–4): 29–36.
39. Chen X, Weigel D, Ganslandt O, Buchfelder M, Nimsky C. Prediction of visual field deficits by diffusion tensor imaging in temporal lobe epilepsy surgery. Neuroimage 2009; 45(2): 286–297.
40. Kuhnt D, Bauer MH, Becker A, Merhof D, Zolal A, Richter M et al. Intraoperative visualization of fiber tracking based reconstruction of language pathways in glioma surgery. Neurosurgery 2012; 70(4): 911–919.
41. Zolal A, Hejčl A, Vachata P, Bartoš R, Humhej I, Malucelli A et al. The use of diffusion tensor images of the corticospinal tract in intrinsic brain tumor surgery – a comparison with direct subcortical stimulation. Neurosurgery 2012; 71(2): 331–340.
42. Catani M, Thiebaut de Schotten M. A diffusion tensor imaging tractography atlas for virtual in vivo dissections. Cortex 2008; 44(8): 1105–1132.
43. Zolal A, Vachata P, Hejčl A, Bartoš R, Malucelli A, Nováková M et al. Anatomy of the supraventricular portion of the pyramidal tract. Acta Neurochirurgica 2012; 154(6): 1097–1104.
44. Tijssen RH, Jansen JF, Backes WH. Assessing and minimizing the effects of noise and motion in clinical DTI at 3 T. Hum Brain Mapp 2009; 30(8): 2641–2655.
45. Mukherjee P, Chung SW, Berman JI, Hess CP, Henry RG. Diffusion tensor MR imaging and fiber tractography: technical considerations. AJNR Am J Neuroradiol 2008; 29(5): 843–852.
46. Yaşargil MG, Ture U, Yaşargil DC. Surgical anatomy of supratentorial midline lesions. Neurosurg Focus 2005; 18(6B): E1.
47. Fernández-Miranda JC, Rhoton AL jr, Alvarez-Linera J, Kakizawa Y, Choi C, de Oliveira EP. Three-dimensional microsurgical and tractographic anatomy of the white matter of the human brain. Neurosurgery 2008; 62 (6 Suppl 3): 989–1026.
48. Choi CY, Han SR, Yee GT, Lee CH. Central core of the cerebrum. J Neurosurg 2011; 114(2): 463–469.
Štítky
Paediatric neurology Neurosurgery NeurologyČlánok vyšiel v časopise
Czech and Slovak Neurology and Neurosurgery
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