Skip to main content

Standard Parafascicular Approaches to Subcortical Regions

  • Chapter
  • First Online:
Subcortical Neurosurgery

Abstract

Surgical access to subcortical brain lesions remains challenging due to limited visualization, narrow corridors for instrument maneuverability, and the delicate nature of the cortical and subcortical structures at risk. The success of minimally-invasive neurological surgery hinges upon effective utilization of modern neuroimaging for diagnosis and preoperative patient and approach selection, intimate knowledge of subcortical anatomy, delicate microsurgical technique, and adequate utilization of adjuvant techniques to preserve functionality and maximize safe resection. Minimally-invasive techniques strive to minimize trauma to surrounding tissues and thusly protect white matter fascicles, preserve neurological function, and reduce iatrogenic morbidity. Transsulcal-parafascicular corridors to subcortical and intraventricular regions were described based upon cadaveric, functional MRI, and diffusion tensor imaging (DTI) studies.

In this chapter, illustrative cases are used to describe anatomical and DTI considerations related to the white matter fibers involved in standard parafascicular approaches (anterior, posterior, and lateral) to subcortical regions.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 84.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 159.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Abbreviations

AF:

Arcuate fasciculus

CF:

Cingulate fasciculus

DTI:

Diffusion tensor imaging

FAT:

Frontal aslant tract

IFOF:

Inferior fronto-occipital fascicle

ILF:

Inferior longitudinal fascicle

MRI:

Magnetic resonance imaging

NIHSS:

National Institute of Health Stroke Score

OR:

Optic radiations

SFS:

Superior frontal sulcus

SLF:

Superior longitudinal fasciculus

References

  1. Geffen G, Walsh A, Simpson D, Jeeves M. Comparison of the effects of transcortical and transcallosal removal of intraventricular tumours. Brain. 1980;103(4):773–88.

    Article  CAS  PubMed  Google Scholar 

  2. Kelly PJ, Goerss SJ, Kall BA. The stereotaxic retractor in computer-assisted stereotaxic microsurgery. Technical note. J Neurosurg. 1988;69(2):301–6.

    Article  CAS  PubMed  Google Scholar 

  3. Yasargil MG, Cravens GF, Roth P. Surgical approaches to “inaccessible” brain tumors. Clin Neurosurg. 1988;34:42–110.

    CAS  PubMed  Google Scholar 

  4. Solaroglu I, Beskonakli E, Kaptanoglu E, Okutan O, Ak F, Taskin Y. Transcortical-transventricular approach in colloid cysts of the third ventricle: surgical experience with 26 cases. Neurosurg Rev. 2004;27(2):89–92.

    Article  PubMed  Google Scholar 

  5. Engh JA, Lunsford LD, Amin DV, Ochalski PG, Fernandez-Miranda J, Prevedello DM, et al. Stereotactically guided endoscopic port surgery for intraventricular tumor and colloid cyst resection. Neurosurgery. 2010;67(3 Suppl Operative):ons198–204; discussion ons-5.

    Google Scholar 

  6. Recinos PF, Raza SM, Jallo GI, Recinos VR. Use of a minimally invasive tubular retraction system for deep-seated tumors in pediatric patients. J Neurosurg Pediatr. 2011;7(5):516–21.

    Article  PubMed  Google Scholar 

  7. Labib MA, Shah M, Kassam AB, Young R, Zucker L, Maioriello A, et al. The safety and feasibility of image-guided BrainPath-mediated transsulcul hematoma evacuation: a multicenter study. Neurosurgery. 2017;80(4):515–24.

    Article  PubMed  Google Scholar 

  8. Bauer AM, Rasmussen PA, Bain MD. Initial single-center technical experience with the BrainPath system for acute intracerebral hemorrhage evacuation. Oper Neurosurg (Hagerstown). 2017;13(1):69–76.

    Article  PubMed  Google Scholar 

  9. Kassam AB, Engh JA, Mintz AH, Prevedello DM. Completely endoscopic resection of intraparenchymal brain tumors. J Neurosurg. 2009;110(1):116–23.

    Article  PubMed  Google Scholar 

  10. Nagatani K, Takeuchi S, Feng D, Mori K, Day JD. High-definition exoscope system for microneurosurgery: use of an exoscope in combination with tubular retraction and frameless neuronavigation for microsurgical resection of deep brain lesions. No Shinkei Geka. 2015;43(7):611–7.

    PubMed  Google Scholar 

  11. Eliyas JK, Glynn R, Kulwin CG, Rovin R, Young R, Alzate J, et al. Minimally invasive transsulcal resection of intraventricular and periventricular lesions through a tubular retractor system: multicentric experience and results. World Neurosurg. 2016;90:556–64.

    Article  PubMed  Google Scholar 

  12. Flores BC, Whittemore AR, Samson DS, Barnett SL. The utility of preoperative diffusion tensor imaging in the surgical management of brainstem cavernous malformations. J Neurosurg. 2015;122(3):653–62.

    Article  PubMed  Google Scholar 

  13. Bander ED, Jones SH, Kovanlikaya I, Schwartz TH. Utility of tubular retractors to minimize surgical brain injury in the removal of deep intraparenchymal lesions: a quantitative analysis of FLAIR hyperintensity and apparent diffusion coefficient maps. J Neurosurg. 2016;124(4):1053–60.

    Article  PubMed  Google Scholar 

  14. Soares JM, Magalhaes R, Moreira PS, Sousa A, Ganz E, Sampaio A, et al. A Hitchhiker’s guide to functional magnetic resonance imaging. Front Neurosci. 2016;10:515.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Day JD. Transsulcal parafascicular surgery using BrainPath® for subcortical lesions. Neurosurgery. 2017;64(CN_suppl_1):151–6.

    Google Scholar 

  16. Jennings JE, Kassam AB, Fukui MB, Monroy-Sosa A, Chakravarthi S, Kojis N, et al. The surgical white matter chassis: a practical 3-dimensional atlas for planning subcortical surgical trajectories. Oper Neurosurg (Hagerstown). 2018;14(5):469–82.

    Article  Google Scholar 

  17. Nimsky C, Ganslandt O, Hastreiter P, Wang R, Benner T, Sorensen AG, et al. Intraoperative diffusion-tensor MR imaging: shifting of white matter tracts during neurosurgical procedures--initial experience. Radiology. 2005;234(1):218–25.

    Article  PubMed  Google Scholar 

  18. Nimsky C, Ganslandt O, Merhof D, Sorensen AG, Fahlbusch R. Intraoperative visualization of the pyramidal tract by diffusion-tensor-imaging-based fiber tracking. NeuroImage. 2006;30(4):1219–29.

    Article  PubMed  Google Scholar 

  19. Ribas GC, Yasuda A, Ribas EC, Nishikuni K, Rodrigues AJ, Jr Surgical anatomy of microneurosurgical sulcal key points. Neurosurgery. 2006;59(4 Suppl 2):ONS177–210; discussion ONS-1.

    Google Scholar 

  20. Monroy-Sosa A, Chakravarthi SS, Fukui MB, Kura B, Jennings JE, Celix JM, et al. White matter-governed superior frontal sulcus surgical paradigm: a radioanatomic microsurgical study-part I. Oper Neurosurg (Hagerstown). 2020;19(4):E343–E56.

    Article  PubMed  Google Scholar 

  21. Gungor A, Baydin S, Middlebrooks EH, Tanriover N, Isler C, Rhoton AL Jr. The white matter tracts of the cerebrum in ventricular surgery and hydrocephalus. J Neurosurg. 2017;126(3):945–71.

    Article  PubMed  Google Scholar 

  22. Baker CM, Burks JD, Briggs RG, Smitherman AD, Glenn CA, Conner AK, et al. The crossed frontal aslant tract: a possible pathway involved in the recovery of supplementary motor area syndrome. Brain Behav. 2018;8(3):e00926.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Koutsarnakis C, Liakos F, Kalyvas AV, Skandalakis GP, Komaitis S, Christidi F, et al. The superior frontal transsulcal approach to the anterior ventricular system: exploring the sulcal and subcortical anatomy using anatomic dissections and diffusion tensor imaging tractography. World Neurosurg. 2017;106:339–54.

    Article  PubMed  Google Scholar 

  24. Shinoura N, Suzuki Y, Yamada R, Tabei Y, Saito K, Yagi K. Damage to the right superior longitudinal fasciculus in the inferior parietal lobe plays a role in spatial neglect. Neuropsychologia. 2009;47(12):2600–3.

    Article  CAS  PubMed  Google Scholar 

  25. Jang SH, Jang WH. Ideomotor apraxia due to injury of the superior longitudinal fasciculus. Am J Phys Med Rehabil. 2016;95(8):e117–20.

    Article  PubMed  Google Scholar 

  26. Yucel M, Wood SJ, Fornito A, Riffkin J, Velakoulis D, Pantelis C. Anterior cingulate dysfunction: implications for psychiatric disorders? J Psychiatry Neurosci. 2003;28(5):350–4.

    PubMed  PubMed Central  Google Scholar 

  27. Fornito A, Yucel M, Wood SJ, Bechdolf A, Carter S, Adamson C, et al. Anterior cingulate cortex abnormalities associated with a first psychotic episode in bipolar disorder. Br J Psychiatry. 2009;194(5):426–33.

    Article  PubMed  Google Scholar 

  28. Ribas GC. The cerebral sulci and gyri. Neurosurg Focus. 2010;28(2):E2.

    Article  PubMed  Google Scholar 

  29. Alves RV, Ribas GC, Parraga RG, de Oliveira E. The occipital lobe convexity sulci and gyri. J Neurosurg. 2012;116(5):1014–23.

    Article  PubMed  Google Scholar 

  30. Martino J, da Silva-Freitas R, Caballero H, Marco de Lucas E, Garcia-Porrero JA, Vazquez-Barquero A. Fiber dissection and diffusion tensor imaging tractography study of the temporoparietal fiber intersection area. Neurosurgery. 2013;72(1 Suppl Operative):87–97; discussion -8.

    Google Scholar 

  31. Yagmurlu K, Vlasak AL, Rhoton AL, Jr. Three-dimensional topographic fiber tract anatomy of the cerebrum. Neurosurgery. 2015;11 Suppl 2:274–305; discussion.

    Google Scholar 

  32. Ivanova MV, Isaev DY, Dragoy OV, Akinina YS, Petrushevskiy AG, Fedina ON, et al. Diffusion-tensor imaging of major white matter tracts and their role in language processing in aphasia. Cortex. 2016;85:165–81.

    Article  PubMed  Google Scholar 

  33. Kamali A, Sair HI, Radmanesh A, Hasan KM. Decoding the superior parietal lobule connections of the superior longitudinal fasciculus/arcuate fasciculus in the human brain. Neuroscience. 2014;277:577–83.

    Article  CAS  PubMed  Google Scholar 

  34. Monroy-Sosa A, Jennings J, Chakravarthi S, Fukui MB, Celix J, Kojis N, et al. Microsurgical anatomy of the vertical rami of the superior longitudinal fasciculus: an intraparietal sulcus dissection study. Oper Neurosurg (Hagerstown). 2019;16(2):226–38.

    Article  PubMed  Google Scholar 

  35. Grefkes C, Fink GR. The functional organization of the intraparietal sulcus in humans and monkeys. J Anat. 2005;207(1):3–17.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Luckmann HC, Jacobs HI, Sack AT. The cross-functional role of frontoparietal regions in cognition: internal attention as the overarching mechanism. Prog Neurobiol. 2014;116:66–86.

    Article  PubMed  Google Scholar 

  37. Culham JC, Kanwisher NG. Neuroimaging of cognitive functions in human parietal cortex. Curr Opin Neurobiol. 2001;11(2):157–63.

    Article  CAS  PubMed  Google Scholar 

  38. Sanai N, Martino J, Berger MS. Morbidity profile following aggressive resection of parietal lobe gliomas. J Neurosurg. 2012;116(6):1182–6.

    Article  PubMed  Google Scholar 

  39. Andersen RA, Andersen KN, Hwang EJ, Hauschild M. Optic ataxia: from Balint’s syndrome to the parietal reach region. Neuron. 2014;81(5):967–83.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. Jang SH, Kim SH, Kwon HG. The safe area in the parieto-occipital lobe in the human brain: diffusion tensor tractography. World Neurosurg. 2015;83(6):982–6.

    Article  PubMed  Google Scholar 

  41. Koutsarnakis C, Liakos F, Kalyvas AV, Liouta E, Emelifeonwu J, Kalamatianos T, et al. Approaching the atrium through the intraparietal sulcus: mapping the sulcal morphology and correlating the surgical corridor to underlying fiber tracts. Oper Neurosurg (Hagerstown). 2017;13(4):503–16.

    Article  PubMed  Google Scholar 

  42. De Benedictis A, Duffau H, Paradiso B, Grandi E, Balbi S, Granieri E, et al. Anatomo-functional study of the temporo-parieto-occipital region: dissection, tractographic and brain mapping evidence from a neurosurgical perspective. J Anat. 2014;225(2):132–51.

    Article  PubMed  PubMed Central  Google Scholar 

  43. Catani M, Jones DK, Donato R, Ffytche DH. Occipito-temporal connections in the human brain. Brain. 2003;126(Pt 9):2093–107.

    Article  PubMed  Google Scholar 

  44. Saur D, Kreher BW, Schnell S, Kummerer D, Kellmeyer P, Vry MS, et al. Ventral and dorsal pathways for language. Proc Natl Acad Sci U S A. 2008;105(46):18035–40.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  45. Ffytche DH, Blom JD, Catani M. Disorders of visual perception. J Neurol Neurosurg Psychiatry. 2010;81(11):1280–7.

    Article  PubMed  Google Scholar 

  46. Rubino PA, Rhoton AL Jr, Tong X, Oliveira E. Three-dimensional relationships of the optic radiation. Neurosurgery. 2005;57(4 Suppl):219–27; discussion -27.

    PubMed  Google Scholar 

  47. Kier EL, Staib LH, Davis LM, Bronen RA. MR imaging of the temporal stem: anatomic dissection tractography of the uncinate fasciculus, inferior occipitofrontal fasciculus, and Meyer’s loop of the optic radiation. AJNR Am J Neuroradiol. 2004;25(5):677–91.

    PubMed  PubMed Central  Google Scholar 

  48. Baydin S, Gungor A, Tanriover N, Baran O, Middlebrooks EH, Rhoton AL Jr. Fiber tracts of the medial and inferior surfaces of the cerebrum. World Neurosurg. 2017;98:34–49.

    Article  PubMed  Google Scholar 

  49. Kamali A, Flanders AE, Brody J, Hunter JV, Hasan KM. Tracing superior longitudinal fasciculus connectivity in the human brain using high resolution diffusion tensor tractography. Brain Struct Funct. 2014;219(1):269–81.

    Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Gustavo Pradilla .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2022 Springer Nature Switzerland AG

About this chapter

Check for updates. Verify currency and authenticity via CrossMark

Cite this chapter

Barbero, J.M.R., Bray, D., Pradilla, G. (2022). Standard Parafascicular Approaches to Subcortical Regions. In: Zada, G., Pradilla, G., Day, J.D. (eds) Subcortical Neurosurgery. Springer, Cham. https://doi.org/10.1007/978-3-030-95153-5_10

Download citation

Publish with us

Policies and ethics