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Original Article

Biofield potential simulation as a novel adjunt modality for continuous monitoring of breast lesions: a 3D numerical model

, &
Pages 40-52 | Published online: 09 Jul 2009
 

Abstract

Breast cancer is a disease characterized by the uncontrolled growth of abnormal cells. Early detection of this disease is the most effective way to reduce mortality. Although several new technologies show promise for improved capability of diagnosis, none have yet proved superior to traditional, X-ray film mammography in screening for breast cancer. More evaluation and development of new imaging tools and of promising skin surface electrical potential techniques is required and warranted. In the present study, we propose a theoretical three-dimensional, simplified and realistic model of the female breast to distinguish the surface biopotential in different types of breast abnormalities. We developed an inhomogeneous female breast model, closer to the actual, by considering the breast as a hemisphere with various layers of unequal thickness in supine condition. In order to determine the potential distribution developed, isotropic homogeneous conductivity was assigned to each of these compartments and the volume conductor problem was solved using finite element method. Richardson extrapolation for grid invariance test was used to ensure the results are of reliable accuracy. The simulation results show that the surface potentials are sensitive to the presence of tumour, location and placement of the electrodes.

Nomenclature
ϕ=

Electric potential (mV)

σ=

Tissue space variant conductivity tensor (Ωm)−1

Iv=

Source term (mA m−3)

=

Nabla operator

x,y,z=

Cartesian coordinates (m)

n=

Unit normal vector

J=

Magnitude of applied current density (m Am−2)

f=

Discrete solution

h=

Grid spacing

g=

Functions defined in continuum that do not depend on any discretization

HOT=

Higher order terms

r=

Refinement ratio

p=

Orders of the basic numerical method

E1=

Estimated fractional error

ϵ=

Error band

A1=

Actual fractional error of fine grid solution

GCI=

Grid convergence index

Ep=

Asymptotic range of errors

Nomenclature
ϕ=

Electric potential (mV)

σ=

Tissue space variant conductivity tensor (Ωm)−1

Iv=

Source term (mA m−3)

=

Nabla operator

x,y,z=

Cartesian coordinates (m)

n=

Unit normal vector

J=

Magnitude of applied current density (m Am−2)

f=

Discrete solution

h=

Grid spacing

g=

Functions defined in continuum that do not depend on any discretization

HOT=

Higher order terms

r=

Refinement ratio

p=

Orders of the basic numerical method

E1=

Estimated fractional error

ϵ=

Error band

A1=

Actual fractional error of fine grid solution

GCI=

Grid convergence index

Ep=

Asymptotic range of errors

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