TY - JOUR
T1 - Neuroimaging in HIV infection
T2 - a preliminary quantitative MRI study and review of the literature
AU - Kent, Thomas A.
AU - Hillman, Gilbert R.
AU - Levin, Harvey S.
AU - Guinto, Faustino
AU - Kaye, Alan R.
AU - Casper, Karen
N1 - Funding Information:
Supported by NIH RO3 MH49552-01 (TAK).
PY - 1993
Y1 - 1993
N2 - A review of both functional and structural imaging of the brain through the course of HIV infection leads to a fairly consistent pattern of involvement. Brain involvement in asymptomatic HIV positive individuals remains controversial. However, in symptomatic subjects, less controversy exists. Subcortical structures appear to be vulnerable early, followed by cortical and eventual diffuse involvement. Specific abnormal findings include symmetrical atrophy, hyperintense white matter lesions, both subcortical and cortical ventricular enlargement and focal metabolic abnormalities. It has' not been possible to correlate the specific underlying pathological mechanisms responsible for each of -these lesions and the pathophysiology probably involves multiple mechanisms, both direct and indirect. Some of these lesions are reversible with treatment, but the full implications of this reversibility with regard to pathogenesis and prognosis remain speculative. New evidence presented here suggests that both gray and white matter are involved in the atrophy.
AB - A review of both functional and structural imaging of the brain through the course of HIV infection leads to a fairly consistent pattern of involvement. Brain involvement in asymptomatic HIV positive individuals remains controversial. However, in symptomatic subjects, less controversy exists. Subcortical structures appear to be vulnerable early, followed by cortical and eventual diffuse involvement. Specific abnormal findings include symmetrical atrophy, hyperintense white matter lesions, both subcortical and cortical ventricular enlargement and focal metabolic abnormalities. It has' not been possible to correlate the specific underlying pathological mechanisms responsible for each of -these lesions and the pathophysiology probably involves multiple mechanisms, both direct and indirect. Some of these lesions are reversible with treatment, but the full implications of this reversibility with regard to pathogenesis and prognosis remain speculative. New evidence presented here suggests that both gray and white matter are involved in the atrophy.
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U2 - 10.1016/S0960-5428(06)80043-4
DO - 10.1016/S0960-5428(06)80043-4
M3 - Article
AN - SCOPUS:0345298225
SN - 0960-5428
VL - 3
SP - 129
EP - 140
JO - Advances in Neuroimmunology
JF - Advances in Neuroimmunology
IS - 2
ER -