Let’s spend some time in this #tweetorial on the dermatologic manifestations of this potentially paraneoplastic disease!
First, a question: What is necessary to make a diagnosis of DM?
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None of the above! DM is a clinical diagnosis, which is why getting the exam right is super important! That said a biopsy CAN help with getting to a diagnosis, but it’s not necessary.
So let’s start! Heliotrope rash! This poikilodermatous erythema occurs around the eyes. 2/
Remember though that exams are different across skin tone. Heliotrope can look a lot more subtle in someone with more melanated skin. That rash can also include the rest of the face! 3/
Shawl sign (back) and V sign (upper chest) is another one we all learn in medical school. What’s the deal with all these physical exam findings?
Well, they are all in photodistributed patterns. Additionally, they are generally poikilodermatous! 4/
Poikilodermatous? Say what? It’s just a fancy way we refer to skin that has 4 changes: Hyperpigmentation, hypopigmentation, erythema, and atrophy. The point is heliotrope, shawl sign, v-sign, other findings, are usually all similarly “poikilodermatous” changes in the skin. 5/
All right, what else did you learn about DM? I’m guessing…. Gottron! These are now called Atrophic dermal papules of DM (ADPDM). Importantly, even if you don’t have papules and just have the erythema, that’s still c/w DM! 6/
Since we’re on the hands, let’s zoom in on the fingers & look for the other telltale signs you’re looking for. Specifically, the ragged cuticles and dilated periungual capillary loops! Notice how those blood vessels are plump & super noticeable compared to your own (I hope!). 7/
This is where most people stop thinking about skin findings. But did you know there are more? You can see calcinosis cutis in DM (not just in systemic sclerosis!). It’s much more common in Juvenile DM, but adults can get it too. 8/
DM can also present with flagellate erythema! Check out my other brief thread on this. 4 things classically cause this:
And you can also get that poikilodermatous change on your lateral thighs. This is called holster sign (pic 1)! You can also get keratodermatous changes to your hands called “mechanic’s hands (pic 2). 10/
Not only are these exam findings important for the diagnosis of DM, but also because different findings can be associated with different risk. Mechanic’s hands + holster sign make me concerned for anti-synthetase syndrome!
Which Autoantibody is linked with this?
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Jo-1 Is associated with anti-synthetase syndrome.
TIF-1 and NXP-2 are associated with increased risk of malignancy!
OMG-7 is just silly. 12/
While we’re on the topic, let’s discuss malignancy risk. It’s been reported in up to 40% of ADULT patients with DM (not really a concern in juvenile DM). Most commonly reported associations are ovarian, lung, colon, breast, GI, and lymphoma.
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Given these concerns, what is the work up for a new DM patient in regards to malignancy? I was taught the following:
Age-appropriate cancer screening
Transvaginal US + CA-125 (if applicable)
CT Scan Neck to pelvis
Although a topic of debate, the risk of malignancy goes back to baseline after 3-5 years, so I was trained to do the aforementioned periodically until that point.
What about autoantibodies? Here’s a list of what I check and why! 15/
The proximal mm weakness I’ll leave to #rheumtwitter to discuss, but this is where I’m testing muscle strength in derm clinic. Remember to ask about washing hair and standing from a seated position ;)
Can you get DM without muscle weakness?
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You can! If you have all the skin findings, but NO muscle involvement on exam, labs, nor imaging, you might have something called Clinically amyopathic dermatomyositis (CADM).
This is presumptive for 6 months, after which if all is still negative, it's confirmed CADM!
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This #tweetorial is getting much too long, so we’ll leave treatment to the next time. Before we get to the summary, a huge thank you to @DrScottElman for giving me feedback! A huge thanks to @visualdx for the photos. And I hope #rheumtwitter will add as they see fit! 18/
SUMMARY
✅DM is a clinical diagnosis. Biopsy can help but not necessary.
✅The consistent findings on exam are poikiloderma and photodistribution.
✅Screening for cancer should happen!
✅You can get DM without muscle involvement!
19/19
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It's been ages since I've put out a #dermtwitter#tweetorial, so I thought what better way than to share a diagnosis that was the original motivator for me to become a dermatologist! A 🧵 on:
What is Pemphigus Vegetans? This is where breaking down the terms can be super helpful. It's the diagnosis we give when pemphigus has the morphology of vegetative plaques.
Let's start with an easy question. When you hear "umbilicated papule," what is your inclination for diagnosis?
I'd guess you're thinking of molluscum contagiosum (MC), amirite?
Well, which one of those photos is molluscum?
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I'm not telling you the answer yet! Stay tuned!
Here's the deal about MC - it's a poxvirus that is SUPER common in kids. So if your patient is a child with umbilicated papules, MC is a great diagnosis.
If an adult, then still think MC, but more likely sexually transmitted. 3/
If you find yourself in the role of a consultant, be kind. The person paging you is asking for help from you, the expert. It's an opportunity to help & educate.
Remember how nervous you might've been the 1st time you called a consult!
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Yes, all those "silly consults" add up to be more work. But remember, you are the expert now, and what is "silly" to you may be truly confounding to the primary team. Something that might seem so simple to you is only that way because of your training, and that's pretty great.
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I still remember the times I got annoyed or angry about a "silly consult." Without fail, I always regretted how I reacted on the phone. It's so much easier to be kind, than to apologize later. You are serving as an ambassador for your specialty to the rest of the hospital!
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Just a few years ago, Sezary Syndrome (SS) was thought to be the leukemic variant of Mycosis Fungoides (MF). We basically thought people had MF, it would keep getting worse, and then it would turn into SS.
But patients often present with either the classic SS exam (red all over, super itchy), or with MF. Some patients would progress from MF--> SS, but it's the minority. So it became clear these are two different processes.
For that reason, we've changed how we think about it... 3/
Let's start by establishing that Wilson Disease is a multisystem process wherein copper deposits in various tissues (liver, brain, eyes) because of improper transport.
A mutation in ATP7B causes this, and the depositional process leads to disease manifestations. 2/
Given the organs Cu2+ deposits in, you see neurologic effects, Kayser Fleischer rings in the eyes, and of course, liver disease.
While here👇, we see the always memorized, rarely seen, Kayser Fleischer rings, let's focus on the liver...