Lc. Meiners et al., Relevance of temporal lobe white matter changes in hippocampal sclerosis -Magnetic resonance imaging and histology, INV RADIOL, 34(1), 1999, pp. 38-45
Citations number
36
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Medical Research Diagnosis & Treatment
RATIONALE AND OBJECTIVES. TO evaluate the diagnostic relevance of ipsilater
al atrophy of the collateral white matter in the parahippocampal gyrus (ACW
Mp) and temporal lobe gray/white matter demarcation loss (GWDL) on magnetic
resonance imaging in patients with histologically confirmed hippocampal sc
lerosis, In the second part of this investigation, histologic specimens wer
e analyzed to find an explanation for GWDL.
METHODS. Retrospective visual assessment of hippocampal signal intensity an
d size and of ACWMp and GWDL was performed using 4- to 5-mm coronal T2-weig
hted spin-echo magnetic resonance images of 80 patients with histologically
proven hippocampal sclerosis and of 30 age matched controls without epilep
sy. Frequency of occurrence and likelihood ratios of ACWMp and GWDL were ca
lculated and their contribution to the diagnosis of hippocampal sclerosis w
as assessed, particularly in patients with no or restricted hippocampal abn
ormalities (either high signal or smaller size) on magnetic resonance imagi
ng. The second part of the study involved the morphologic histologic assess
ment of neocortical temporal lobe specimens of all patients. Myelin density
was evaluated in specimens of a subgroup of six patients with hippocampal
sclerosis and GWDL on MRI and six patients with hippocampal sclerosis witho
ut GWDL.
RESULTS. ACWMp was found in 68% and GWDL in 65% of patients with hippocampa
l sclerosis on magnetic resonance imaging, Both features had an infinite po
sitive likelihood ratio. Sixty-two patients (77.5%) had concomitant hippoca
mpal signal increase and smaller size. Eighteen patients (22.5 %) had no or
restricted hippocampal abnormalities on magnetic resonance imaging. When u
sing ACWMp and GWDL as additional diagnostic parameters, 13 of these 18 pat
ients were more unambiguously diagnosed as having hippocampal sclerosis. No
significant morphologic differences were found between GWDL-positive and G
WDL-negative specimens, A significantly lower average myelin stain was foun
d in the white matter of the GWDL-positive group compared to the GWDL-negat
ive group.
CONCLUSIONS. ACWMp and GWDL can improve the visual diagnosis of hippocampal
sclerosis, particularly in patients with no or restricted hippocampal abno
rmalities. These results suggest that loss of myelin may be the underlying
cause of GWDL in association with hippocampal sclerosis.