Deep brain structures are frequently
used as targets in neurosurgical
procedures. However, the boundaries of
these structures are often not visible in
clinically used MR and CT
images. Techniques based on anatomical
atlases and indirect targeting are used to
infer the location of these targets
intraoperatively. Initial errors of such
approaches may be up to a few millimeters,
which is not negligible. E.g. subthalamic
nucleus is approximately 4x6 mm in the
axial plane and the diameter of globus
pallidus internus is approximately 8 mm,
both of which are used as targets in deep
brain stimulation surgery. To increase the
initial localization accuracy of deep brain
structures we have developed an atlas-based
segmentation method that can be used for
the surgery planning [1]. The atlas is a high
resolution MR head scan of a healthy
volunteer with nine deep brain structures
manually segmented (Fig. 1). The quality of the
atlas image allowed for the segmentation of
the deep brain structures, which is not
possible from the clinical MR head scans of
patients.
Figure
1: 3D models of the segmented deep brain
structures of the atlas: inferior view
with an axial image slice (left) and
oblique view with three orthogonal image
slices (right). The abbreviations are:
putamen (PU), caudate nucleus (CN), globus
pallidus internus (GPi), globus pallidus
externus (GPe), anterior commissure (AC),
posterior commissure (PC), thalamus (TH),
subthalamic nucleus (STN), and substantia
nigra (SN). The figure is from [1] and it
is used with permission; Copyright ©
2008 Society of Photo-Optical
Instrumentation Engineers (SPIE). All
rights reserved.
The subject image is non-rigidly
registered to the atlas image using a two
stage method. Results of the registration
are shown in Figs. 2 and 3. The obtained
transformation is used to map the segmented
structures from the atlas to the subject
image (Fig 4). We tested the approach on
five subjects. The quality of the
atlas-based segmentation was evaluated by
visual inspection of the third and lateral
ventricles, putamena, and caudate nuclei,
which are visible in the subject MR
images. The agreement of these structures
for the five tested subjects was
approximately 1 to 2 mm.
Figure
2: Axial checkerboard slices of the atlas
image and a registered subject image after
the initial affine alignment (left),
Stage-1 of registration (center) and the
final Stage-2 registration (right). Note
the progressive improvement of alignment
of the ventricles, PU and CN from
initialization to the final registration.
The figure is from [1] and it is used with
permission; Copyright © 2008 Society
of Photo-Optical Instrumentation Engineers
(SPIE). All rights reserved.
Figure
3: Axial (right), sagittal (top left) and
coronal (bottom left) checkerboard slices
of the atlas image and non-rigidly
registered subject image. Note the good
alignment of the ventricles, PU and CN at
the boundaries of the checkerboards. Some
apparent variations are because of
difference in the intensities and
protocols of the atlas and the subject
image. The figure is from [1] and it is
used with permission; Copyright ©
2008 Society of Photo-Optical
Instrumentation Engineers (SPIE). All
rights reserved.
Figure
4: Deep brain region axial slices of the
atlas image (top row) and a registered
subject (bottom row) overlaid with the
contours of the manually segmented atlas
deep brain structures. The color coding is
the same as in Fig. 1. The misalignment of
the posterior part of the right lateral
ventricle (bottom row, left) is due to a
significant lateral ventricle shape
difference between the subject and the
atlas. The figure is from [1] and it is
used with permission; Copyright ©
2008 Society of Photo-Optical
Instrumentation Engineers (SPIE). All
rights reserved.
References:
[1] Khan, M., Mewes, K., Gross, E. R.,
Skrinjar, O., "Atlas-based Segmentation of
Deep Brain Structures using Non-Rigid
Registration", SPIE Medical Imaging 2008,
San Diego, CA, USA, Vol. 6918, February
2008. LINK