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Neurosurgery. 2012 Mar;70(1 Suppl Operative):145-56; discussion 156. doi: 10.1227/NEU.0b013e31822efcae.

Visual pathway study using in vivo diffusion tensor imaging tractography to complement classic anatomy.

Author information

1
Brigham and Women's Hospital, Department of Neurosurgery, Harvard Medical School, Boston, Massachusetts 02115, USA.

Abstract

BACKGROUND:

Knowledge of the individual course of the optic radiations (ORs) is important to avoid postoperative visual deficits. Cadaveric studies of the visual pathways are limited because it has not been possible to separate the OR from neighboring tracts accurately and results may not apply to individual patients. Diffusion tensor imaging studies may be able to demonstrate the relationships between the OR and neighboring fibers in vivo in individual subjects.

OBJECTIVE:

To use diffusion tensor imaging tractography to study the OR and the Meyer loop (ML) anatomy in vivo.

METHODS:

Ten healthy subjects underwent magnetic resonance imaging with diffusion imaging at 3 T. With the use of a fiducial-based diffusion tensor imaging tractography tool (Slicer 3.3), seeds were placed near the lateral geniculate nucleus to reconstruct individual visual pathways and neighboring tracts. Projections of the ORs onto 3-dimensional brain models were shown individually to quantify relationships to key landmarks.

RESULTS:

Two patterns of visual pathways were found. The OR ran more commonly deep in the whole superior and middle temporal gyri and superior temporal sulcus. The OR was closely surrounded in all cases by an inferior longitudinal fascicle and a parieto/occipito/temporo-pontine fascicle. The mean left and right distances between the tip of the OR and temporal pole were 39.8 ± 3.8 and 40.6 ± 5.7 mm, respectively.

CONCLUSION:

Diffusion tensor imaging tractography provides a practical complementary method to study the OR and the Meyer loop anatomy in vivo with reference to individual 3-dimensional brain anatomy.

PMID:
21808220
PMCID:
PMC3236807
DOI:
10.1227/NEU.0b013e31822efcae
[Indexed for MEDLINE]
Free PMC Article

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