The Pathology Course Cometh. Part 3: Posts.
I’ll be honest: studying pathology can be overwhelming at times. Especially in the beginning. (more…)
I’ll be honest: studying pathology can be overwhelming at times. Especially in the beginning. (more…)
If you’re just starting your first pathology class, and you’re a little anxious, we’ve got help for you! (more…)
Next week marks the start of classes for a lot of medical, dental, nursing, physician assistant, medical technology, veterinary, and other allied health students. (more…)
Hereditary hemorrhagic telangiectasia is one of a handful of diseases that I could never really get into my head. I don’t know why, because the name is so descriptive – it tells you exactly what the distinctive features of the disease are.
Maybe it’s because my professors used the older name for this disease – Osler-Weber-Rendu disease – which is about as non-descriptive a name as you can get. Good thing we’re getting away from eponymous disease names. They’re charming, but they make life really hard for students.
Back to hereditary hemorrhagic telangiectasia. Let’s take a closer look at this name – because once you know what the words mean, you’ll understand the disease without having to use brute memorization.
We’ll look at the words out of order, so that the explanation makes sense.
Hereditary: This is an autosomal dominant disorder. For boards (I can’t imagine an exam question on this, but who knows?), you might want to know that the mutated genes in this disorder encode parts of the TGF-β signaling pathway.
Telangiectasia: This is a great name, because everything you need to know is right there in the name. Too bad we don’t have time to cover some simple Greek and Latin word roots in medical school, because once you know a few, you can easily figure out what words mean. Telangiectasia comes from three Greek words:
τέλος (telos): “end” (For example: telomeres are the little things on the ends of chromosomes.)
So telangiectasias are abnormal dilations of the very ends (tiny capillaries or venules) of blood vessels. They often occur in the skin and mucous membranes, and sometimes they look like tiny little spiders, but sometimes they just look like red blotches (check out the image above). Telangiectasias can also occur in the respiratory, gastrointestinal, and urinary tracts. Telangiectasias are not neoplastic (there aren’t any new, neoplastic vessels); they’re just malformations of existing vessels.
Hemorrhagic: Sometimes telangiectasias can rupture, causing nosebleeds, GI bleeding or hematuria.
That’s it! Now you know 🙂
Q. I am a 4th year medical student in Sri Lanka. I’m having trouble with this anemia question:
A 65 year old Finnish bachelor is a self-proclaimed heavy drinker. (more…)
Before I get to fuscus, I have to say that I have HAD it with this month. Normally I start complaining about February around mid-January, and continue on every day until people start avoiding me. This year, I thought I could rise above it. I tried thinking positively. I tried reading Jung and Frankl to address my existential crisis. Last night I was up late listening to Jordan Peterson, and I thought I was doing pretty well.
But this morning, after coming out to a car completely encased in ice (not exaggerating), after seeing the sky the same color as the ground (greyish white) YET AGAIN, and after some other crap that I won’t go on about, I’m done. February just sucks. It’s not me, it’s you, February.
Since I sat down intending to write about the very nice Latin word fuscus, I thought maybe I’d look up the origin of the word February and see if there was some Latin that could help make me feel better. And there was! So I’m sharing what I found in the hopes that it may help others who have February issues.
February is usually said to be derived from the Latin februum, meaning anything that purifies or consecrates. This doesn’t fit my view of this month, but whatever. According to a prominent Roman grammarian (what a cool job, seriously) named Censorinus, who wrote De Die Natali (The Birthday Book) in 238 AD, there were tons of februamenta (rites of purification) going on in Rome during this time of the calendar year. Part of the purification was agricultural (clearing away dead stuff and getting the fields ready for planting). But it wasn’t just fields – houses, material items, and even the Romans themselves were februa (purified) in different ways, using different rites.
In Roman tradition, February was originally the last month of the year, and, according to Ovid, it was “consecrated to the shades of the dead.” So along with acts of propitiation (appeasement, I had to look it up too), there were acts of purification to protect the living from evil spirits and also to banish the spirits at the end of the year so that the new year could begin in purity.
The image above is a drawing of the month of February from a fourth century calendar. The caption describes how to placate the ghosts that roam the earth in February. Okay – keeping angry ghosts from haunting the living – now we’re getting somewhere.
Yes, there is. Some sources suggest that February actually comes from feber, a word which the Romans used to describe lamentation. YES! That’s it. I KNEW there had to be something in the name of this miserable month that reflected its true nature. Okay, the Romans were lamenting their deceased. But still. It fits. For the rest of the month, I’m going to say Lamentation instead of February and see if anyone notices.
For those of you brave enough to read this far, here’s a happy thing to offset all the misery. As you may know, there are a bunch of pigments you can see sometimes in tissues. One of them is called lipofuscin. It’s known as the wear-and-tear pigment, because it accumulates with age. Lipofuscin is composed of a bunch of lipids and proteins and has a yellow-brown appearance. It has no clinical significance – but you need to know it exists so you don’t confuse it with something else yellow-brown, like hemosiderin.
Here’s the good part. The first half of lipofuscin makes sense, since it’s composed partly of lipids. The second half is derived from the Latin word fuscus, which means dingy, brown, or dark – great Latin word choice, since lipofuscin has a dingy, brown appearance. So that’s why “obfuscate” means “to make unclear or obscure.” And it may be where we got the word “dusk” (from Middle English dosk, which came from Old English dox, which probably came from our Latin hero fuscus).
This is the weird kind of thing that makes me happy. I have no idea why finding the Latin connection between two seemingly unrelated words should make me happy in such disproportionate measure – or happy at all – but it does.
In this month of Lamentation, I’ll take happiness where I can get it.
Q. I’m a little confused about the difference between an aortic dissection and a false aneurysm.
In diagrams of aortic dissection, it looks like all three layers of the vessel have been damaged and blood is leaking out of the vessel BUT still contained by connective tissue etc. Isn’t that what a false aneurysm is? So what’s the difference between the two?
A. I can see what you mean – diagrams of aortic dissections can be misleading!
Diagrams of aortic dissection (like this one above, from Wikipedia) often focus on the three types of dissections. The point of these diagrams is just to show the place in the aorta where the dissection begins (near the heart vs. more distally). They can be kind of misleading, though, if they don’t clearly depict how the blood tunnels through the wall of the aorta. Like you described, it can look more like the aorta has actually ruptured all the way through, and the blood is collecting outside the aorta.
So let’s quickly review the definitions of false aneurysm and dissection.
In a false aneurysm, all three walls of the vessel have been broken through, and blood collects just outside the vessel. It doesn’t tunnel down or up into the wall of the vessel at all. After some time, the blood organizes and becomes firm – kind of like a blood clot – and it prevents further blood from escaping the damaged vessel.
In a dissection, only the inner portion of the vessel wall is damaged. Blood enters into that damaged area, and tunnels up or down within the wall of the vessel. Unlike a false aneurysm, in which blood bursts through all three layers of the vessel, in a dissection, the outer layers of the vessel are still intact, and blood forms a channel within the vessel wall itself.
So you had the right idea! It was just the diagram that threw you off. In the diagram above, the arrangement of the two little white arrows incorrectly implies that blood is busting all the way through the aorta at a single point – but the rest of the aortic wall looks intact. To really show what’s happening in an aortic dissection, the wall of the aorta should be more clearly depicted, and the second arrow should point up or down within the wall itself, showing the path of blood as forms a tunnel within the vessel wall.
Q. I have Googled and YouTubed this thing to death, and I still can’t grasp the meaning of “differentiation.” It seems the opposite of its definition. To “differentiate” means to recognize what makes something different. But according to your post on tumor differentiation, well-differentiated tumors resemble (don’t look different from) their tissue of origin. I would think if something is well-differentiated, it would look very different from the thing it’s being compared to. Why is the use here opposite of its meaning?
A. I totally get where you’re coming from. It’s REALLY frustrating in pathology when things are described in terms that don’t seem to make sense. You are not alone in questioning the use of this term!
The problem is that the word in question – differentiation – has a specific meaning in the real world. You’re exactly right in your definition: to differentiate between two things means to recognize what’s different or unique.
So you’d think that “differentiation” in the pathology world would mean the same thing: the recognition of things that are unique, different, or not the same. By logical reasoning, then, a “differentiated” tumor would be one that looked different from its cell of origin. And you’d think a “well-differentiated” tumor would be one that looked very different from its cell of origin.
Unfortunately, “differentiation” doesn’t have the same definition in the pathology world. So we have to put aside our logic and knowledge of vocabulary for a moment, irritating as that may be, and learn a new definition for this word.
When we’re talking about tumors, the definition of “differentiation” is simply this: the degree to which tumor cells resemble their cell of origin. A well-differentiated tumor is one in which the tumor cells look very much like their cell of origin. A poorly-differentiated tumor (like the poorly-differentiated squamous cell carcinoma shown above) is one in which the tumor cells barely resemble their cell of origin.
That’s it. Yes, it’s an annoying word choice, because it is used here in a way that seems counterintuitive. But maybe it’s not as far off as it seems.
I think about it (okay, rationalize it) this way. When cells are really immature, they don’t have a lot of features that make them look different from other cells. Myeloblasts don’t look very different than lymphoblasts, for example. So we could say that these immature cells are undifferentiated; it’s hard to tell what kind of cell they really are, and hard to tell them apart from other cells.
The same thing is true of the cells in poorly-differentiated tumors! The cells show practically no features that give away their identity; it’s hard to even tell what kind of cells they are. They are, in effect, undifferentiated.
If you think about “differentiation” this way (undifferentiated cells lack identifying features; it’s hard to tell what kind of cell they are), then the concept of tumor differentiation is a little easier to swallow. A little.
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Q. I have a quick question on the cell of origin in leukemia. In our pharmacology class, we went through a section on cancer. There was a slide that said leukemia is a tumor of hematopoietic stem cells. But leukemia involves more than just hematopoietic stem cells, right? I think I remember from our pathology class that leukemia can also involve cells downstream of hematopoietic stem cells.
A. You’re absolutely right! Which means you really understood the heme part of our pathology class! Just to back up a bit: all leukemias arise from hematopoietic cells (either myeloid or lymphoid cells). But not all leukemias arise in hematopoietic stem cells. Let’s take a look.
All of the chronic myeloproliferative disorders, for example, originate in stem cells. As a result, when you look in the blood and bone marrow, you see a proliferation of all different kinds of myeloid cells (red cells, neutrophils, and megakaryocytes) at all stages of maturation (neutrophils, myelocytes, metamyelocytes, etc.).
In most of the chronic myeloproliferative disorders, a particular myeloid cell line dominates (in chronic myeloid leukemia (CML), for example, most of the malignant cells are neutrophils and precursors) – but because of the stem cell origin, there are other malignant myeloid cells present as well.
Here’s a cool thing. You’d think that the stem cell of origin in these chronic myeloproliferative disorders would be a myeloid stem cell, right? I mean, these disorders are composed of all kinds of myeloid cells – so the origin should be a myeloid stem cell.
It turns out that the stem cell involved is actually a very young stem cell – it hasn’t even decided whether it wants to be myeloid or lymphoid! We know this because the characteristic genetic abnormality (for example, the Philadelphia chromosome in CML) is also present in lymphocytes. That explains why when CML evolves into blast crisis, the blasts may be either myeloid or lymphoid.
Acute promonocytic leukemia, for example, originates in a promonocyte (a stage of development between monoblast and monocyte). This means that when you look at the blood and bone marrow, you see mostly promonocytes (the cells in the image above with the lovely tissue-paper-like nuclei). Cells of other myeloid cell lineages (like red cells or neutrophils) are not present. These types of leukemias are a lot more straightforward.
This kind of mis-statement (“all leukemias arise from stem cells”) happens a lot when people talk about hematopoietic diseases. Even the names of diseases are often stated incorrectly (e.g., “acute lymphoid leukemia” or “acute lymphocytic leukemia” instead of “acute lymphoblastic leukemia”). Heme is an area that many people shy away from, for some reason. I love it and find it really straightforward, but depending on how it’s taught, it can seem really confusing.
If you’re struggling with heme, there are tons of heme-related posts here on Pathology Student. You might also find my Complete Hematopathology Guide useful; it covers all the main hemepath stuff in a straightforward, no-BS way.
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