- [Voiceover] Inflammatory Bowel Disease
is a group of disorders that includes
both Crohn's Disease and Ulcerative Colitis.
Now unfortunately, the exact cause of
Inflammatory Bowel Disease is not well understood.
However, both types of Inflammatory Bowel Disease
are the result of an inappropriate inflammatory response
that results in chronic intestinal damage,
as well as potentially serious
and life-threatening complications.
Now despite having considerable overlap
in their clinical presentation,
as well as a similar underlying mechanism,
the two types of inflammatory bowel disease
have many important epidemiologic,
as well as pathologic, distinctions.
And these distinctions are pretty important
for the diagnosis and treatment of the diseases.
Now before we dive into the pathology
of inflammatory bowel disease,
let's talk briefly about how common these diseases are,
and some of the risk factors.
So, how common is inflammatory bowel disease?
Well, this may seem like a fairly simple question,
but it's not quite as easy as one might think.
Because the prevalence, or the number of
people with disease at any specific time,
varies significantly depending on the location.
So, in countries that are more rural
and less industrially developed,
such as much of South America and Africa,
the prevalence is much lower than in
more well developed or well industrialized
and more urban areas of the world,
such as much of North America and Europe.
So let's focus on North America and Europe, here.
For Crohn's disease, the prevalence in North America
and Europe is somewhere between 250 and 300
per 100,000 individuals.
Whereas ulcerative colitis has a slightly lower prevalence,
and that's somewhere between 50 and 100 per 100,000 people.
To put this into perspective, in a city the size of London
with a population of about 8.3 million people,
a prevalence of 300 per 100,000
would mean that about 25,000 people have Crohn's disease,
and that's about the same amount of people
as there are students at King's College in London.
Whereas with Crohn's disease,
with a prevalence of 100 per 100,000 people,
that means that in London, there are probably
somewhere around 8,300 people
living with ulcerative colitis,
which is about the number of people
who visit Buckingham Palace everyday.
Now as I mentioned earlier, the exact cause
of inflammatory bowel disease is not really well understood.
However, there are a few distinct risk factors
for both Crohn's disease and ulcerative colitis.
And the first one to mention is age.
In Crohn's disease, the incidence,
meaning the rate at which people are diagnosed,
is highest between the ages of 15 and 35.
Now ulcerative colitis also tends to have
a similar peak incidence around the ages of 15 to 35,
however, it is something known as a bi-modal distribution.
And this means that there's a second peak,
and this occurs during the ages of 60 to 80
when, for some reason, individuals once again
become more likely to develop the disease.
Now the next risk factor is that of a family history.
Now both types of inflammatory bowel disease
have an underlying genetic predisposition,
which is made evident in that an individual
with an immediate family member,
meaning one of their brothers or their sisters
or their parents,
that person is going to have a higher chance
of developing either Crohn's disease or ulcerative colitis.
Now for Crohn's disease, this risk is a little bit higher
at 10 percent.
Meaning that someone with an immediate family member
who has Crohn's disease has a 10 percent chance
of also developing the disease,
which is about 30 times higher than that
of the general population.
And with ulcerative colitis, family history
also is an important risk factor,
but it's not quite as significant,
where the risk is about two percent,
meaning that someone who has an immediate family member
with ulcerative colitis has about a two percent risk
of also developing ulcerative colitis
sometime in their life.
And that is about 10 times higher
than that of the general population.
And then there are a few other risk factors
that are important to mention.
For Crohn's disease, a very important risk factor
is a history of smoking,
as well as what we talked about earlier
in that someone living in urban areas,
especially of industrialized countries,
is at a high risk of developing Crohn's disease.
Then with ulcerative colitis, an important risk factor
is having a diet that is high in total fat intake
and then also having a history of salmonella
or campylobacter infections.
And salmonella and campylobacter are types of bacteria
that can cause an infection of the G.I. tract.
Now that we have a little bit better understanding
of what exactly inflammatory bowel disease is,
let's discuss some of the pathologic changes
that occur in these two diseases,
which are very important for distinguishing
Crohn's disease from ulcerative colitis.
And let's start with the location of the inflammation.
Now if you break down the name of many medical conditions,
it will give you a better understanding
of what the disease is.
Unfortunately, with Crohn's disease,
it's named after Burrill Bernard Crohn,
who described the condition back in 1932.
So it's name doesn't really tell us much about the disease.
Ulcerative colitis is a little bit different
on the other hand.
So itis stands for inflammation,
and col is for the colon, which is just another way
of saying the large intestine.
So ulcerative colitis is an ulcerative
or an inflammatory ulcer of the colon,
which is this part of the G.I. tract right here.
Now in ulcerative colitis, the lesions
almost invariably begin here in the rectum
and then they move backwards through the intestine
in a continuous fashion and are completely contained
within the large intestine.
So about 50 percent of people who have also colitis
will have inflammation that starts in the rectum
and then moves just a little ways back
into the sigmoid colon.
So this is the sigmoid colon.
It's called the sigmoid because it kind of looks like an S.
Then about 30 percent of people with ulcerative colitis
will have what's called subtotal colitis.
This means that the inflammation extends
beyond the rectum and the sigmoid colon
back into the descending and maybe into transverse colon,
but not the entire colon.
It's subtotal or less than total,
less than all of the colon.
And the last 20 percent of people
will have total colitis,
meaning that the inflammation is going to extend
all the way back through their entire colon.
So it's going to include the ascending, the transverse,
the descending, the sigmoid and the rectum.
So they have total inflammation.
Now in Crohn's disease, the inflammation can occur
anywhere from the mouth to the anus,
but it doesn't occur in this continuous fashion
that ulcerative colitis does.
In Crohn's disease, it's discontinuous,
meaning that someone may have inflammation
in the terminal ileum
or the last part of the small intestine,
maybe here in the colon.
Another spot in the small intestine.
They could have it in the esophagus and in the mouth,
but they'll have gaps between these inflamed areas
with normal G.I. tract and then another
area of inflammation, then normal G.I. and so on.
And so these are known as skip lesions
because they'll skip over normal segments of bowel.
Now the most common place for the inflammation to occur
in Crohn's disease is the terminal ileum,
which is the very last segment of the small intestine.
And the second most common place
that these inflammatory lesions occur in Crohn's disease
is the large intestine.
Now aside from the location of inflammation,
the microscopic pathology of Crohn's disease
and ulcerative colitis are distinct from one another.
So here we have a diagram of the wall
of a segment of the intestine here.
So imagine this is the inside of the intestine
where the food kind of travels through
and then gets absorbed through the wall
of the intestine into the bloodstream.
Now there are three distinct layers to the intestinal wall.
The one closest to the inside of the intestine
is known as the mucosa.
Then below that is the submucosa,
which is named submucosa because it's below the mucosa,
and then the third and innermost layer
is known as the muscularis externa,
and this is because it contains the muscle fibers
that help move food along through our digestive tract.
Now the exact mechanism and cause of the inflammation
in inflammatory bowel disease isn't well understood,
but what seems to happen is that individuals
have a genetic predisposition
for developing inflammatory bowel disease.
That's we mentioned they're hereditary,
or that family history as a risk factor.
But this genetic predisposition isn't quite enough.
In addition, there's some sort of trigger.
And this trigger here is the part that's not
quite as well understood.
It could be caused by some sort of change
in the composition of the normal intestinal bacterial flora
within the large and small intestine,
or it could be the result of some sort of
G.I. infection, like the campylobacter or the salmonella
that we talked about earlier.
But what happens is when you get this combination
of the genetic predisposition and some sort of
environmental trigger, that causes the immune system
to attack and damage the G.I. tract.
Now so far, this part of the mechanism
is the same for both Crohn's disease and ulcerative colitis.
However, over time, the damage that occurs
to this intestinal wall at a microscopic level differs.
So let's take a look at this.
Now over here on the left, we have a picture
of the intestinal wall in someone with Crohn's disease.
And I have a couple of cells here
and they're a little bit out of scale
but the idea is that this is a macrophage
and this here is a neutrophil.
Now macrophages and neutrophils are normal cells
that are part of the immune system.
But for some reason in Crohn's disease
and ulcerative colitis, they begin to attack
the intestinal wall.
And overtime, this inflammatory response
causes damage to the intestinal wall.
And as you can see here in Crohn's disease,
this inflammation extends, these lesions extend
through all three layers of the intestinal wall.
So this is known as transmural inflammation.
And in Latin, transmural literally means through the wall.
So the inflammation is going all the way through
the intestinal wall.
And in addition to these immune cells causing this damage,
there's infiltration of the wall of the intestine
with another type of immune cell.
It's known as a lymphocyte, which I have demonstrated here
with these kind of loop, little blue dots
that are infiltrating the wall.
So you have transmural inflammation
with lymphocytic infiltration.
And in addition, the immune system over time
forms another type of microscopic lesion,
which is known as a non-caseating granuloma,
which is a sign of chronic inflammation.
Now in ulcerative colitis, the macrophages and neutrophils
are also causing damage to the intestinal wall,
but the microscopic appearance is somewhat different.
In ulcerative colitis, this inflammation
doesn't extend all the through the intestinal wall
as it does in Crohn's disease.
It only extends through the mucosa and the submucosa.
So in ulcerative colitis, you have mucosal
and submucosal inflammation.
So this distinction between transmural inflammation
and mucosal and submucosal inflammation
is one of the most important pathologic distinctions
between Crohn's disease and ulcerative colitis.
Now overtime, these lesions can worsen
and they can cause many different complications.
And some of them are the same with for both Crohn's disease
and ulcerative colitis, although some of them
are characteristic of one form of inflammatory bowel disease
or the other.
So let's take a look at that.
So the first pathologic complication we'll discuss
is something known as a crypt abscess.
And occasionally, what happens is this inflammation,
as it progresses, will result in kind of this
walled off pocket of space.
And if that pocket includes some bacteria,
that can get infected and form an abscess.
And these crypt abscesses aren't just in Crohn's disease,
they can also occur in ulcerative colitis.
Now often times, these abscesses, they may not cause
a whole lot of symptoms other than perhaps
just a mild fever.
But if they rupture and they spill
this kind of infective fluid out into the abdominal cavity,
they can cause a very serious
or potentially even life-threatening complication
known as peritonitis.
So if these abscesses are found,
they're normally treated with IV antibiotics
as well as drainage.
And by treating that, it prevents the rupture
and the development of the peritonitis.
So another one of these pathologic complications
that occurs primarily in Crohn's disease
is something known as a fistula.
So imagine here that you have section
of the bowel or maybe it's the small intestine
that has a Crohn's disease lesion.
Now it's in the abdominal cavity,
so it's bumping up next to another section of bowel.
Maybe this is the large intestine.
But what can happen overtime is eventually,
this inflammation gets worse and worse
and forms almost a tunnel
between the two structures.
So you can see that the lumen of one section of bowel
is actually in communication with
another section of bowel.
So this communication of this tunnel
is known as a fistula.
Now these fistulas don't just occur between
two segments of the bowel, they can occur
between pretty much anything that a Crohn's lesion
is bumped up next to.
So that can include things like the skin,
the bladder and the vagina.
Now these fistulas can cause a significant amount of pain,
as well as severe infection.
So you can imagine that if there's a fistula
between a segment of the bowel and the bladder,
what happens is the bladder, which is normally sterile,
now has a direct connection to the bacteria
of the intestine.
So you can get a very serious bladder infection.
So if a fistula is found in someone with Crohn's disease,
it's usually going to be removed with surgery.
Now for ulcerative colitis, there's another
one of these pathologic findings that is important to note,
and this is known as a pseudopolyp.
Now overtime, as the inflammation
of the intestinal wall worsens,
the flattening out or thinning
of the mucosal and the submucosal layers
can occur in an uneven pattern.
And what it leaves is these kind of pseudopolyps,
or it looks like a polyp sticking out
of the intestinal wall, but it's called a pseudopolyp
because it isn't a growth out,
it's actually that everything around that structure
has been thinned out.
And so that is a pseudopolyp,
which is a characteristic of ulcerative colitis.
So inflammatory bowel disease is a group of disorders
that's caused by an appropriate inflammatory response
that results in this chronic intestinal change.
But the two types, Crohn's disease and ulcerative colitis,
although they have a similar underlying mechanism,
they can be defined pathologically based on location
of the lesions, as well as the microscopic appearance
of the pathology.
So in Crohn's disease, the lesions can be located
anywhere from the mouth to the anus,
and they occur in this discontinuous, skip lesion pattern.
Whereas in ulcerative colitis,
the inflammation nearly always begins in the rectum
and continues in a continuous fashion
backwards through the colon
and almost never exits the large intestine.
Now for the microscopic findings on the pathology,
Crohn's disease is defined by inflammation
that goes through all three layers of the intestinal wall,
which is known as that transmural inflammation,
as well as these non-caseating granulomas.
Then ulcerative colitis, the inflammation is contained
only within the first two layers of the intestinal wall,
which is known as the mucosal and submucosal inflammation.
This is important because it's the location
of the lesions that is going to define
the clinical presentation of the disease
in terms of the signs and symptoms,
as well as the means for diagnosis.
Whereas the microscopic pathology
is going to have an effect on the potential complications,
as well as the treatment of the disease.