Interactive Transcript
0:00
We're going to continue in the differential
0:03
diagnosis of demyelinating disorders.
0:06
The next entity I'd like to talk about is
0:08
acute disseminated encephalomyelitis.
0:11
This is a diagnosis that is more frequently
0:14
created or diagnosed in children than it is in adult.
0:19
It is a typically monophasic disorder,
0:24
although it can have recurrences.
0:27
It typically occurs within two to four weeks
0:30
after a viral infection or immunization.
0:34
Therefore,
0:35
because children are getting vaccinated more
0:37
commonly than adults and also getting viral
0:40
infections more commonly than adults,
0:42
it is seen more commonly in children.
0:44
This is an autoimmune disorder that is thought
0:47
to be a delayed type hypersensitivity
0:50
reaction to myelin basic protein,
0:52
leading to an attack on the white matter.
0:55
It, like multiple sclerosis,
0:57
can affect the brain, can affect the spine,
1:00
and is in the differential diagnosis for
1:02
cases of optic neuritis as well.
1:05
There is a more aggressive form that may be
1:08
hemorrhagic and that is much more fulminant
1:12
and has a worse prognosis.
1:15
On this slide,
1:17
anything that's labeled with a P
1:19
refers to pediatric variety of ADEM,
1:22
whereas anything that refers to an A is the
1:25
adult variety of ADEM.
1:27
So, as you can see,
1:29
cortical involvement occurs much more frequently
1:32
in pediatric cases than in adult cases,
1:36
whereas periventricular white matter involvement
1:39
is more common in the adults than the children.
1:42
Deep gray matter involvement,
1:44
by that, we're usually talking about
1:46
the basal ganglia and the thalami,
1:48
as opposed to in the cerebellum,
1:50
is more frequent in children.
1:52
Brain stem involvement and cerebellar involvement,
1:55
more frequent in children.
1:57
Spinal cord ADEM does occur.
2:00
When it occurs,
2:01
it is more frequent in children
2:02
than in the adult population.
2:04
That involvement of deep gray matter is the
2:08
distinguishing feature between it
2:11
and other demyelinating disorders,
2:13
including multiple sclerosis.
2:15
Here we have a patient who has a much
2:17
more fulminant fluffy disease,
2:20
as opposed to the Dawson fingers-like appearance
2:24
in the periventricular location
2:26
of multiple sclerosis.
2:28
What one is seeing is involvement
2:30
of the thalamus
2:33
in this case,
2:35
as well as the subcortical white matter
2:37
going out to the cortical surface of the brain.
2:41
We don't really see those classic sort of flame
2:44
shaped demyelinating lesions
2:46
of multiple sclerosis in this individual,
2:49
and in this case,
2:50
we are not seeing any evidence of
2:53
contrast enhancement.
2:54
However,
2:55
just like multiple sclerosis,
2:57
ADEM may show contrast-enhancing lesions.
3:01
Another entity to describe is something
3:05
that is affectionately called MDEM.
3:07
Why is it called MDEM?
3:09
Well, we said that ADEM generally is a monophasic
3:13
disorder that occurs at one point.
3:16
However, if you have recurring bouts of ADEM,
3:20
you may hear them use the term multiphasic
3:25
disseminated encephalomyelitis,
3:27
which is a recurrence of potentially ADEM
3:31
that occurs after steroid withdrawal
3:33
or further infection.
3:35
And one thing you should recognize
3:38
is that ADEM is an autoimmune disorder
3:42
with an attack against the white matter,
3:44
as is multiple sclerosis,
3:46
and sometimes this blurring of the distinction
3:50
between ADEM and MDEM
3:52
and subsequently multiple sclerosis
3:55
because you have recurring neurologic events,
3:59
clinically distinct events that occur over time
4:03
with an MRI pattern that will be showing periventricular
4:08
and subcortical,
4:09
as well as cortical lesions that are typical
4:12
of multiple sclerosis, as well as ADEM.
4:17
So it may be that we are looking at a spectrum
4:21
of disorders that may be elicited by viral
4:25
infections that includes ADEM,
4:28
MDEM and multiple sclerosis,
4:31
and which leads to an autoimmune
4:33
attack on the white matter.
6:03
We're going to continue in the differential
6:06
diagnosis of demyelinating disorders.
6:08
The next entity I'd like to talk about is
6:11
acute disseminated encephalomyelitis.
6:14
This is a diagnosis that is more frequently
6:17
created or diagnosed in children than it is in
6:22
adults. It is a typically monophasic disorder,
6:27
although it can have recurrences,
6:30
it typically occurs within two to four weeks
6:33
after a viral infection or immunization.
6:37
Therefore,
6:38
because children are getting vaccinated more
6:40
commonly than adults and also getting viral
6:43
infections more commonly than adults,
6:45
it is seen more commonly in children.
6:47
This is an autoimmune disorder that is thought
6:50
to be a delayed type hypersensitivity
6:53
reaction to myelin basic protein,
6:55
leading to an attack on the white matter.
6:58
It, like multiple sclerosis,
7:00
can affect the brain, can affect the spine,
7:02
And is in the differential diagnosis for
7:05
cases of optic neuritis as well,
7:08
there is a more aggressive form that may be
7:11
hemorrhagic and that is much more fulminant
7:15
and has a worse prognosis.
7:18
On this slide,
7:20
anything that's labeled with a p refers
7:22
to pediatric variety of ADEM,
7:25
whereas anything that refers to an A is the
7:28
adult variety of ADEM. So, as you can see,
7:32
cortical involvement occurs much more frequently
7:35
in pediatric cases than in adult cases,
7:39
whereas periventricular white matter involvement
7:42
is more common in the adults than the children.
7:45
Deep gray matter involvement,
7:47
by that we're usually talking about
7:49
the basal ganglia and the thalami,
7:51
as opposed to in the cerebellum,
7:53
is more frequent in children.
7:55
Brain stem involvement and cerebellar
7:57
involvement more frequent in children.
8:00
Spinal cord ADEM does occur.
8:03
When it occurs,
8:04
it is more frequent in children
8:05
than in the adult population.
8:07
That involvement of deep gray matter is the
8:11
distinguishing feature between it and
8:14
other demyelinating disorders,
8:16
including multiple sclerosis.
8:18
Here we have a patient who has a much
8:20
more fulminant fluffy disease,
8:23
as opposed to the Dawson fingers-like appearance
8:27
in the period of triculocation
8:29
of multiple sclerosis.
8:31
What one is seeing is involvement
8:33
of the thalamus
8:36
in this case,
8:38
as well as the subcortical white matter going
8:41
out to the cortical surface of the brain.
8:44
We don't really see those classic sort of flame
8:46
shaped demyelinating lesions of multiple
8:50
sclerosis in this individual,
8:52
and in this case,
8:53
we are not seeing any evidence of
8:56
contrast enhancement. However,
8:58
just like multiple sclerosis,
9:00
ADEM may show contrast enhancement.
9:03
Lesions.
9:04
Another entity to describe is something
9:08
that is affectionately called MDEM.
9:10
Why is it called MDEM?
9:12
Well,
9:12
we said that ADEM generally is a monophasic
9:16
disorder that occurs at one point.
9:19
However, if you have recurring bouts of ADEM,
9:23
you may hear them use the term multiphasic
9:28
disseminated encephalomyelitis,
9:30
which is a recurrence of potentially ADEM that
9:34
occurs after steroid withdrawal
9:36
or further infection.
9:38
One thing you should recognize is that ADEM is
9:43
an autoimmune disorder with an attack against
9:46
the white matter, as is multiple sclerosis,
9:49
and sometimes this blurring of the distinction
9:53
between ADEM and MDEM and subsequently multiple
9:58
sclerosis because you have recurring
10:00
neurologic events clinically.
10:02
Distinct events that occur over time with an MRI
10:08
pattern that will be showing periventricular
10:11
and subcortical,
10:12
as well as cortical lesions that are typical
10:15
of multiple sclerosis as well as ADEM.
10:20
So it may be that we are looking at a spectrum
10:24
of disorders that may be elicited by viral
10:28
infections that includes ADEM,
10:31
MDEM and multiple sclerosis,
10:34
and which leads to an autoimmune
10:36
attack on the white matter.
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