The topic now brings us to encephalitis.
We’ll make sure that we organize our thoughts before we move on.
Up until this point, we have pretty much looked at meningitidis, CNS infections,
and now we are dealing with infection of the brain parenchyma. Picture that.
Confusion, delirium, focal neurologic, seizures, and coma.
May I asked you something? If your patient has meningitis,
how likely is it that your patient may have seizures?
If it was strictly meningitis, maybe, not necessarily.
Seizures could also be a possibility because we have encephalitis.
The main causes of seizures in patients with HSV encephalitis are related to viral induced hyperexcitability
and the host immune response related to elevated body temperature.
The latter is more important in infants than young children.
Now, the infections that come into the following categories, arboviruses
including your St. Louis, Eastern/Western Equine, West Nile virus.
Enteroviruses and where we will be spending time with will be HSV-1 Herpes.
If your patient is in a state of immunocompromised maybe cytomegalo, EBV, or even perhaps varicella-zoster.
What's my topic? Encephalitis.
And you'll notice for the most part, these are viruses that are commonly found as ideologies.
Our topic is herpes simplex encephalitis but here we're dealing with HSV-1.
What we'll do here is to divide HSV-1 and HSV-2 and then I will highlight to you
what parts of brain are being affected with either type of viral infection.
This must be black and white for you otherwise a clinical presentation on your boards or in clinical practice
is going to be difficult and if you miss it, I am going to be very upset.
Most commonly in children, young adults. That's why I'll be upset.
Most common in children, in young adults.
What parts of the brain will be affected?
You should know that it's the frontal and temporal lobe.
Seizures could also be a possibility because we have encephalitis
which then behaves as a space occupying lesion.
Now, HSV-1 in terms of pathology, once again, please make sure that you're familiar with, what parts of the brain?
The temporal and frontal, you focus on that.
Here, the brain is undergoing such extensive damage that we have necrotization
and we have often hemorrhagic, dangerous.
As soon as you hear about HSV-1 or herpes in general, you should be thinking about Tzanck
and then, what kind of inclusion bodies? Cowdry.
And then the CSF, you should be thinking about PCR, polymerase chain reaction
as being the most accurate diagnostic procedure. This is HSV-1.
Now, with HSV-1 we have a child that's being affected, do not waste time.
You get a history and you suspect there's mood and memory in such that's taking place
and now, at this point treatment, you begin IV acyclovir as soon as possible.
Do not waste time in a child because the brain is still developing. This is HSV-1.
We're gonna move on to HSV-2 where the presentation is a little bit different.
With the HSV-2 this is then referred to as being your herpetic viral meningitis.
Granted, we also call this with HSV-1 but HSV-2 is more genital in region, isn't it?
Generalized, what does that mean to you?
Let me make sure that I emphasize this, if it's HSV-1,
you should be thinking about the frontal and temporal lobe that's commonly affected.
If it's HSV-2, generalized encephalitis and usually much more severe.
50% of neonates born by vaginal delivery to women with active primary HSV genital infections,
as soon as you hear about HSV-2, you should be thinking about that all common herpes
and one in five individuals have herpes, so extremely common.
And this is one the twitches, isn't it? Vertical transmission.
And if imagine a baby, a newborn that is born with HSV-2 type of encephalitis, severe.
In AIDS patients, HSV-2 may cause an acute hemorrhagic necrotizing type of encephalitis, dangerous.
Here's the table once again on a CSF findings, guess, what we're focusing upon this time?
Obviously, HSV encephalitis.
The WBC is here will be elevated primarily lymphocytes.
Neutrophils wouldn't be much elevated.
If RBCs would be found, and that's important, remember? Because brain parenchyma.
And we have glucose, well, a little bit higher than protein but your focus should be in RBCs
and with the specifics that we walked through with HSV-1.
What parts of the brain? Good, temporal and frontal.
If it's HSV-2, it's called herpetic type of encephalitis.
And we call it herpetic because if it's 50% of newborns who have -
who are born to a mother that has a primary HSV infection,
that newborn, the brain may be completely necrotized, generalized, severe.
AIDs patient, there is no age group.
As soon as you have a patient who is severely immunocompromised who then can thrive HSV-2, what happens?
Acute hemorrhagic necrotizing type of encephalitis.
Could it be anymore dramatic about HSV?
Here we have another type of viral encephalitis but this is called progressive multifocal leukoencephalopathy.
As soon as you hear about PML, by reflex you should be thinking about JC, JC, JC Virus.
And in pharmacology there's certain drugs that could be then given in which your patient is predisposed to JC virus
and make sure you're quite familiar with those drugs
and in which the patient, amazingly, is susceptible to leukoencephalopathy.
What does that mean to you? What's "leuko" mean? White.
What's "encephalopathy" mean? Damage to the brain parenchyma, multifocal.
So, if there's destruction of your white matter, if we take a look at this imaging study,
you see the areas that are opaque-ish or whitish,
those are the areas in which the brain parenchyma is undergoing demyelination.
Look at this, I said demyelination as soon as your myelin in your CNS, you tell me what kind of cell is?
Good, oligodendrocytes, right? So now, we have virus preferentially, unbelievably
this virus will then prefer the oligodendrocytes, resulting in what? Leukoencephalopathy.
Demyelination, occurs in immunocompromised patients and also think about those drugs.
And PML does not enhance on MRI as opposed to CNS lymphomas and toxoplasmosis.
In those regions we have absence enhancement.
Here, with brain damage, you're gonna find more of your leukoencephalopathic type of findings.
VZV, when would you find this perhaps causing damage or infection of the brain?
Reactivation, and with reactivation you should be thinking about a patient immunocompromised, older,
and of course, this then brings you to a topic of shingles.
But there's a possibility that a brain infection may take place.
We have persistent post-herpetic neuralgia syndrome in up to 10% of patients. Be careful with this.
We say post-herpetic because what is varicella zoster? It's herpes family, isn't it?
Also, associated with known as granulomatous arteritis.
And may cause an acute encephalitis with numerous sharply circumscribed lesions characterized by early demyelination.
Inclusion bodies can be found in the glia and neurons.
Here for the most part, think of reactivation please with varicella zoster virus
and please don't forget about the post-herpetic neuralgia syndrome in up to 10% of your patients.