2/Sphenopalatine ganglion (SPG) is the largest collection of neurons outside the brain—like a mini brain just for your face. It contains sensory, sympathetic, & parasympathetic nerve fibers. Given this, it’s not surprising that it’s felt to contribute to facial pain syndromes
3/SPG is a meeting point for the sensory nerves from V2 (thus related to trigeminal neuralgia) & the sympathetics and parasympathetics from the greater superficial and deep petrosal nerves, which have been implicated in cluster headache, migraine, & other facial pain syndromes.
4/We can see the SPG in the pterygopalatine fossa on MR neurography. We can see V2 in rotundum as well as the greater superficial petrosal (GSP) & deep petrosal nerves forming the vidian nerve right below rotundum in the vidian canal. These come together as the SPG in the PPF.
5/ SPG blocks are classically for cluster HA/trigeminal autonomic cephalgia (TAC) bc of its parasympathetic activation (lacrimation, rhinorrhea, etc) & sympathetic dysfunction (ptosis & miosis)—but it has been found to be effective in other HA and facial pain syndromes
6/The simplest SPG block method is the transnasal topical approach. A cotton swab applicator soaked w/local anesthetic is advanced posterior to the middle turbinate. It is then laid against the mucosa in that region & the anesthetic is absorbed through the mucosa to the SPG.
7/The next more invasive step is to add to the insertion of a curved catheter, to inject local anesthetic, rather than just laying a cotton soaked tip in that region. However, the injected anesthetic is still absorbed through the mucosa to the SPG.
8/A more direct route is to come to the SPG from below, inserting a syringe through the greater palatine foramen of the posterior hard palate & directly injecting upward into the PPF, where the SPG lives. However, there are many significant drawbacks to this method.
9/Finally, the most direct method is from an infrazygomatic approach to the PPF under image guidance to directly inject anesthetic & possibly steroid directly onto the SPG. This has the advantage of targeted & precise delivery. Only drawbacks are technical difficulty & radiation.
10/Which approach is the best? Intranasal is easier and less invasive, but infrazygomatic is more precise. Some studies have suggested precision matters. So don’t be afraid to put your needle where it needs to go to help relieve the patient’s pain.
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@TheAJNR 2/In the lumbar spine, it is all about the degree of canal narrowing & room for nerve roots.
In the cervical spine, we have another factor to think about—the cord.
Cord integrity is key. No matter the degree of stenosis, if the cord isn’t happy, the patient won’t be either
@TheAJNR 3/Cord flattening, even w/o canal stenosis, can cause myelopathy.
No one is quite sure why.
Some say it’s b/c mass effect on static imaging may be much worse dynamically, some say repetitive microtrauma, & some say micro-ischemia from compression of perforators
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.
2/Let’s start w/T1—it is #1 after all! T1 is for anatomy
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
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.
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!
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
Here's a little help on how to do it yourself w/a thread on how to read a head CT!
2/In bread & butter neuroimaging—CT is the bread—maybe a little bland, not super exciting—but necessary & you can get a lot of nutrition out of it
MRI is like the butter—everyone loves it, it makes everything better, & it packs a lot of calories. Today, we start w/the bread!
3/The most important thing to look for on a head CT is blood.
Blood is Bright on a head CT—both start w/B.
Blood is bright bc for all it’s Nobel prizes, all CT is is a density measurement—and blood is denser (thicker) than water & denser things are brighter on CT
MMA fights get a lot of attention, but MMA (middle meningeal art) & dural blood supply doesn’t get the attention it deserves.
A thread on dural vascular anatomy!
2/Everyone knows about the blood supply to the brain.
Circle of Willis anatomy is king and loved by everyone, while the vascular anatomy of the blood supply to the dura is the poor, wicked step child of vascular anatomy that is often forgotten
3/But dural vascular anatomy & supply are important, especially now that MMA embolizations are commonly for chronic recurrent subdurals.
It also important for understanding dural arteriovenous fistulas as well.