17 research outputs found
Reversible Posterior Leucoencephalopathy (PLES) Syndrome
Scientific background: The posterior leucoencephalopathy (PLES) is a
clinico-radiological syndrome characterised by headache, nausea,
vomiting, disturbances in cognition, depressed level of consciousness,
visual abnormalities and convulsions. It is commonly associated with
malignant hypertension, toxemia of pregnancy or use of
immunosuppressive agents.
O b j e c t i v e: We, here, report a case of reversible posterior
leucoencephalopathy syndrome in a patient submitted with headache,
hypertension, quadranopia and the importance of performing cranial
imaging and the benefit of diffusion MRI in the differential diagnosis of
P L E S.
F i n d i n g s: MRI and diffusion MRI studies have been performed in a 35
year old male patient with hypertension and renal failure, and diffuse
posterior system lesions have been found.
C o n c l u s i o n: The patient’s clinical and radiologic recovery occurs
following control of blood pressur
The Effects of Stimulation Frequency Changes on Central Conduction Time in Short Latency SEPs in Multiple Sclerosis Patients.
Background: Somatosensory evoked potentials (SEPs) are widely used
in the electrophysiological diagnosis of multiple sclerosis since 1970s The importance of central conduction time among SEP parameters is
also well known and it is often regarded as being pathological more
often than the absolute latencies.
Objective: In this study our aim was to find out the effects of the
change of stimulus frequencies on absolute latencies and central
conduction time in median SEPs of multiple sclerosis patients.
Material and method: Twenty five multiple sclerosis patients and 15
healthy subjects were taken into the study and median SEPs of 80
extremities were studied. During median SEP recordings the stimulus
frequencies were changed by 2/sec, 4/sec, 6/sec and 9/sec both in
the patient and control groups. N9 peak, N11 peak, N13 peak, N20
peak and N11-13 complex onset latency, N20 onset latency, peak
central conduction time and onset central conduction time have been
determined both in the patient and the control groups. All the
parameters of different stimulation frequencies were compared
statistically with each other both in the patient and the control groups.
The parameters of the patient and the control groups were also
compared statistically with one and other.
Results: The results showed that N20 peak latency, peak central
conduction time, N20 onset latency and onset central conduction time
values were statistically significantly higher in the patient group when
compared with the control group. In the patient group, the values of
peak central conduction time in 4/sec stimulation frequency were
statistically significantly higher than the values in 2/sec stimulation
frequency (p<0.01). The same was true for the values in 6/sec stimulation
frequency when compared with the values in 2/sec stimulation frequency
(p<0.05). There were no such statistically significant results for peak
central conduction time values of the control group when different
stimulation frequencies were applied (p>0.05). In the patient group,
the values of onset central conduction time in 4/sec stimulation
frequency were statistically significantly higher than the values in 2/sec
stimulation frequency (p<0.05). The values in the control group did
not show any statistical differences again (p>0.05).
Conclusions: The results obtained in this study showed us that the
change of the stimulation frequencies in the patient group enhanced
the pathology seen in both peak and central conduction times whereas
the normal controls were immune to this effect. Changing the stimulation
frequency during short latency SEP recordings has not been studied
in multiple sclerosis patients before. We believe that studies on stimulus
frequency changes in SEPs in multiple sclerosis, will be very useful both
for the electrophysiological diagnosis of MS and the physiological
dynamics of SEPs
A Methodological Study on Cervical Responses by Median Nerve Stimulation
Background: Somatosensory evoked potentials (SEPs) have been widely
accepted as a noninvasive, easy tolerated and, useful method in the assesment
of cervical spinal cord conduction. There are different recording and reference
applications for SEP montage in different articles.
Objective: This study has planned to determine the best placement of
electrodes. Material and Methods: We performed Cv2, Cv3, Cv4, Cv5 recording
with Fz or anterior cervical reference points by median nerve stimulation in
30 healthy subjects with an age range of 20-39. We compared the results
obtained from both reference recordings. And also we performed detailed
correlation analysis between latency, amplitude, duration, intercomponent
intervals and age, height, weight, arm lenght, body mass index, (age-20)2.
Findings: In conclusion, according to recording points there was no meaningful
difference as statistically between parameters. Comparing the reference
points; there is an increased possibility to obtain the complex of N11-N13-
N14 waves by using Fz reference electrod. The results also revealed a statistically
significant
correlation between height, arm lenght and, SEP parameters.
Conclusion: We conclude that there were no differences in latency and
amplitude between Cv2, Cv3, Cv4, Cv5 recordings points. We recommend
that the usage Fz reference point for obtaining N11 potential, the usage of
AC reference point for more clear N13 potential
Asymmetrical Lobar Degenerations: Clinical, Neuropsychological, Scanning Data
OBJECTIVE: Asymmetric lobar degenerations are clinical
syndromes which affect primarily one or more than one cerebral lobe and
result progressive language and/or behaviour and/or cognitive dysfunction.
METHODS:
We report the clinical, neuropsychological and
neuroimaging results of 5 patients with asymmetric lobar degeneration
an one or more than one clinical syndrome according to Frontotemporal
Lobar Degeneration: A Consensus on Clinical Diagnostic Criteria.
RESULTS: Asymmetric lobar degeneration may be one of the largest
entities after Alzheimer Disease to cause dementia. Not only frontal lobe
dementia but also progressive language disorder and corticobasal
degeneration syndrome can be produced by frontotemporal lobar
degeneration and both clinical and pathological overlap of the
syndromes can be seen. The recognition of the relationship between the
clinical syndromes has important implications in the diagnosis and
treatment of dementia