Lea Alhilali, MD Profile picture
May 12, 2023 21 tweets 9 min read Read on X
1/Talk about the bases being loaded!

Central skull base has some of the most complicated anatomy & pathology in neuro

Do you know how to approach it?

Here’s a #tweetorial to show you how diagnose lesions at the central skullbase!

#meded #medtwitter #FOAMed #neurosurgery Image
2/Think of the skullbase divisions like different countries—each w/their own culture. Each division has lesions that are specific to it—just like countries have food that are specific to them.

I think the central skullbase looks like Italy, hanging down from the ant. skullbase Image
3/Lesions can involve the central skullbase from below, within, or above

Let’s start from below. Nasopharynx is below the central skullbase. Nasopharyngeal carcinomas (NPC) can invade from below

Using our Italy theme, you can remember this bc NPC look like an Italian meatball Image
4/Central skullbase can also be involved from below by perineural tumor spread, as it is the home of the cranial nerves.

You can remember this w/our Italy theme bc the tumor spreads along the twisty nerves like Italian pasta Image
5/One unique lesion to involve the central skullbase from below is the juvenile angiofibroma. This occurs in teenage boys & is centered at the sphenopalatine foramen. It’s very vascular & commonly causes w/epistaxis

You can remember this bloody tumor bc Italian sauces are RED Image
6/Now let’s look at lesions from within. Lesions arising from the marrow are common in the central skullbase bc it has abundant marrow. Most commonly, it’s metastases & myeloma. You can remember marrow lesions are common here, bc bone marrow is an Italian delicacy Image
7/Unique lesions to the central skullbase that arise from within are notochordal from the notochordal remnants that live in this region.

Using our Italian theme, you can remember this bc Noto is a city in Sicily—we actually vacationed there last year! Image
8/Notochordal lesions are spectrum, ranging from the most aggressive, chordoma, to the more benign ecchordosis physaliphora & benign notochordal cell tumors.

How do you tell these lesions apart from each other & from other skullbase lesions? Image
9/Pathologic hallmark of notochordal cell tumors is physaliphorous cells. Physaliphorous means bubble lover, because the cells look like big empty bubbles.

This makes me think of bubble tea. Unfortunately, bubble tea isn’t Italian to help you remember this, but it is delicious! Image
10/You can think of these bubble cells like water balloons—they are filled with fluid.

So what does a lot of water mean? Bright on T2!

These lesions are super bright on T2 bc they have these water filled cells. Image
11/Most common notochordal lesions are chordoma & ecchordosis. They are actually like twins that were separated at birth.

They look identical to pathologists but they have very different behaviors. In fact, ecchordosis used be called “intradural chordoma.” Image
12/It’s like they were twins separated at birth & raised differently.

Chordoma was raised extradurally, on the wrong side of the tracks, on the rough side of town, away from the safe intradural space—while ecchordosis was coddled by the warm protection of the dura Image
13/Bc chordoma was raised on the wrong side of the dura, it is more like to, well, light up—or enhance on imaging.

Whereas the properly raised ecchordosis is unlikely to find a pipe & light up, so it rarely enhances Image
14/Another finding that can help you differentiate is a bony spur. A bony spur is pathognomonic for ecchordosis.

I remember this bc only a lesion raised in the comfort of the intradural space, very privileged, can afford a Bentley Spur Image
15/In between ecchordosis & chordoma is the benign notochordal cell tumor (BNCT).

It’s like their cousin, who was raised on the wrong side of the tracks (extra-dural) but was somehow able to turn their life around—so they don’t light up

BNCT are extradural but do not enhance Image
16/BNCT is like a kid who made it out the hood growing up extradural to be a success & not light up.

But bc it had a tough time growing up, it was scarred or sclerosed by the experience. So BNCT have sclerosis on CT Image
17/Because of the sclerosis, BNCT can mimic fibrous dysplasia on CT, with mixed lytic & sclerotic findings.

But bc they are a notochordal cell tumor, they are bright on T2 from the physaliphorous cells, unlike fibrous dyplasia which is T2 dark from its fibrous component. Image
18/Another T2 bright central skullbase lesion is chondrosarcoma. It’s aggressive & can mimic a chordoma on MRI.

You can differentiate them by their position. Chordoma is midline, while chondrosarcoma is off midline.

I remember this bc CORE-doma is central or in the core Image
19/I remember chondrosarcoma is off midline bc it’s a Sarcoma & Sarcoma and Side both start w/S.

On CT, you can see rings & arcs matrix. This makes sense bc rings aren’t in the CORE of a planet, they’re along the SIDE. Image
20/Finally, lesions from above.

At the central skull base, these are overwhelming aggressive pituitary adenomas.

Using our Italian theme, I remember this bc pituitary sounds like an Italian insult they might hurl at you with some classic hand gestures😉 Image
21/So now you can use our Italian theme to remember the most common central skullbase lesions that involve this region from below, within, or above.

Please stay tuned for more BASICS of skullBASE as next I will tackle the posterior skullbase. Alla prossima! Image

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More from @teachplaygrub

Nov 20
1/Time to rupture all your misconceptions about aneurysms!

When you see an aneurysm on imaging, do you know if it’s at high risk of rupture?

This month’s @theAJNR SCANtastic shows you which aneurysms are bursting w/risk!

ajnr.org/content/45/11/…Image
2/Aneurysm rupture is a devastating even, as it results in subarachnoid hemorrhage & complications such as hydrocephalus, vasospasm, infarcts, & death.

Preventing it by treating aneurysms before they rupture is key. But you also don’t want to overtreat. Image
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What makes him more likely to rupture are the same things that make aneurysms more likely to rupture Image
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Nov 11
1/Need help reading spine imaging? I’ve got your back!

It’s as easy as ABC!

A thread about an easy mnemonic you can use on every single spine study you see to increase your speed & make sure you never miss a thing! Image
2/A is for alignment

Look for:
(1) Unstable injuries

(2) Malalignment that causes early degenerative change. Abnormal motion causes spinal elements to abnormally move against each other, like grinding teeth wears down teeth—this wears down the spine Image
3/B is for bones.

On CT, the most important thing to look for w/bones is fractures. You may see focal bony lesions, but you may not

On MR, it is the opposite—you can see marrow lesions easily but you may or may not see edema associated w/fractures if the fracture is subtle Image
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Nov 8
1/Raise your hand if you’re confused by the BRACHIAL PLEXUS!

I could never seem to remember or understand it—but now I do & I’ll show you how!

A thread so you will never fear brachial plexus anatomy again! Image
2/Everyone has a mnemonic to remember brachial plexus anatomy.

I’m a radiologist, so I remember one about Rad Techs.

But just remembering the names & their order isn’t enough.

That is just the starting point--let’s really understand it Image
3/From the mnemonic, we start with the roots—the cervical nerve roots.

I remember which roots make up the brachial plexus by remembering that it supplies the hand.

You have 5 fingers on your hand so we start with C5 & we take 5 nerve roots (C5-T1). Image
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Nov 6
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 so that the next time you see a hemorrhage, your guess on when it happened will always be in the right vein! Image
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 memorizeImage
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

So let’s look at T1Image
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Oct 29
1/To call it or not to call it? That is the question!

Feeling wacky & wobbly when it comes to normal pressure hydrocephalus?

Don’t want to overcall it, but don’t want to miss it either!

Check out the latest in NPH w/this month’s @theAJNR SCANtastic!

ajnr.org/content/45/10/…Image
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This begs the question—when do you stop looking & call it idiopathic? When do you suggest it on imaging? Image
3/There’s an iNPH Radscale, which scores 7 different imaging features.

Score above 8 is very sensitive for iNPH.

But who’s going to take out calipers & evaluate SEVEN different imaging findings on every dementia MR?

Also this scale doesn’t predict who will respond to shunting Image
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Oct 18
1/Do radiologists sound like they are speaking a different language when they talk about MRI?

T1 shortening what? T2 prolongation who?

Here’s a translation w/an introductory thread to MRI. Image
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Since it’s anatomic, brain structures will reflect the same color as real life

So gray matter is gray on T1 & white matter is white on T1

So if you see an image where gray is gray & white is white—you know it’s a T1 Image
3/T1 is also for contrast

Contrast material helps us to see masses

Contrast can’t get into normal brain & spine bc of the blood brain barrier—but masses don’t have a blood brain barrier, so when you give contrast, masses will take it up & light up, making them easier to see. Image
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