2/Remember, you can think of pathology at the skullbase like bad things that can happen while running. Bad things can get you from below—like falling into a pothole. They can come from within—like a sudden heart attack, or bad things can strike from above, like a lightning bolt
3/Same thing w/the skullbase—bad things can come from below, within, or above. Lesions from below are potholes tripping you up. Lesions from w/in the skullbase are like heart attacks strikning from inside. Lesions from above are the lightning, hitting the skullbase from above
4/So what lesions come from below, within, or above? This is determined by what tissues live there. Think of the skullbase like a sandwich. Bones of the skullbase are the filling, sandwich between the bread of the sinonasal cavity & intracranial contents
5/But it also matters where a lesion involves the skullbase. The different regions of the skullbase are very different, like different countries. Just like different countries have their own culture & traditions, these different skullbase regions of have their own typical tumors
6/Countries grew different cuisines based on what was plentiful in their area. Like tomatoes grew well in Italy but not England, so Italy has more tomato-based dishes. Same w/the skullbase regions--they have different tumors depending on what tissues are plentiful in their area
7/We’ve previously reviewed anterior & central skullbase. I think the posterior skullbase looks like the circle of the Greek isles. You can remember pathology in this area by thinking Greek!
8/For lesions from below, a unique lesion to the posterior skullbase is paragangliomas, glomus jugulare. It classically has a salt & pepper appearance because of the T2 hyperintense stroma (salt) & dark flow voids (pepper), but bc it’s Greek, let’s call it a Tzatziki appearance
9/For lesions from within, there are no specific lesions—just lesions that are not unique to the skullbase that tend to involve marrow/bones, such as mets/myeloma, Paget’s, etc. But remember, these lesions tend to be multiple—just like there are multiple Greek isles!
10/Lesions from above come from the intracranial contents abutting the skullbase (dura & cranial nerves). Lower CNs at the posterior skullbase commonly form schwannomas. Remember this bc Greek gyros are basically made w/shawarma meat, & these "shawarmomas" look like little gyros
11/These schwannomas can become very large—then I think they look like overloaded gyros!
12/So for every skullbase lesions, you should ask yourself 2 questions:
Which regions is it located? (anterior, central or posterior)
& Where is it arising from? (from below, from within, or from above)
13/The intersection of the answer to these two questions will narrow your differential in this very complex region to only a few entities—possibly even a single entity!
14/So remember, the skullbase may have many parts, many tissues, and many pathologies, but you only need to answer 2 questions to get you to the correct answer!
• • •
Missing some Tweet in this thread? You can try to
force a refresh
1/ I always say, "Anyone can see the bright spot on diffusion images—what sets you apart is if you can tell them why it’s there!”
If you don't why a stroke happened, you can't prevent the next one!
Can YOU tell a stroke’s etiology from an MRI?
Here’s a thread to show you how!
2/First a review of the vascular territories.
I think the vascular territories look a butterfly—w/the ACA as the head/body, PCA as the butt/tail, and MCA territories spreading out like a butterfly wings.
3/Of course, it’s more complicated than that.
Medially, there are also small vessel territories—the lenticulostriates & anterior choroidal.
I think they look like little legs, coming out from between the ACA body & PCA tail.
1/Asking “How old are you?” can be dicey—both in real life & on MRI!
Do you know how to tell the age of blood on MRI?
Here’s a thread on how to date blood on MRI!
After reading this, when you see a hemorrhage, your guess on its age will always be in the right vein!
2/If you ask someone how to date blood on MRI, they’ll spit out a crazy mnemonic about babies that tells you what signal blood should be on T1 & T2 imaging by age.
But mnemonics are crutch—they help you memorize, but not understand
If you understand, you don’t need to memorize
3/If you look at the mnemonic, you will notice one thing—the T1 signal is all you need to tell if blood is acute, subacute or chronic.
T2 signal will tell if it is early or late in each of those time periods—but that type of detail isn’t needed in real life
@TheAJNR 2/Since the prehistoric days of medicine (1979!), we knew that some brain tumor patients treated w/radiation (XRT) initially declined, but then get better.
Today, we see this on imaging, where it looks worse early, but then gets better.
Now we call this pseudoprogression.
@TheAJNR 3/Why does this happen?
XRT induces a lot of inflammatory changes—from initiating the complement cascade to opening the blood brain barrier (BBB)
It’s these inflammatory changes that make the imaging look worse.