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/
SS and MF, although both types of cutaneous T-cell Lymphoma (CTCL), one is thought to be a tumor of circulating memory T-cells (SS), and the other a tumor of resident memory T-cells in the skin (MF). This paper from 2010 outlines it well.
Okay, now that we've established how we think about SS, let's talk exam.
As I mentioned above, classically you see erythroderma (>90% BSA skin redness).
If someone has prolonged erythroderma, which one of the following would you NOT expect to see?
5/
Correct answer: blistering! The point is that ectropion, keratoderma, lymphadenopathy, are all sequelae of prolonged inflammation of the skin, and NOT specific for SS.
Pruritus is usually debilitating in these patients and is a MAJOR problem for QOL. 6/
So if you see someone with erythroderma, how might you work up for SS?
Which of the following tests might you send?
7/
ALL OF THEM!
You might be skeptical about HTLV in all patients. That's fair, but Adult T-cell Leukemia and Lymphoma is a classic culprit for erythroderma too, so if the patient's history/ancestry are right, you might want to consider checking them! 8/
Re: skin biopsy- SS is notoriously hard to get on skin biopsy. You might see the classic CTCL findings (tagging of atypical lymphocytes at the DEJ, pautrier's microabscesses, epidermotropism), or it might just look reactive.
Imma let my #dermpath colleagues weigh in here too! 9/
What REALLY helps is your blood work.
FIRST PEARL: If you're sending a flow, you MUST send a CBC/diff. You need it to calculate absolute values for your flow.
These are the requirements for diagnosing SS on flow: 10/
Remember SS preps? And you'd see if you had >1000 SS cells/uL?
Flow is just the more efficient way of doing that. We're identifying the SS immune phenotype & counting.
That means we care about the CD7- and CD26- subset of the CD4+ cells. But you need >1000/uL for the SS dx! 11/
Okay, let's talk treatment. There is only one cure for SS: allogeneic stem cell transplant. Unfortunately, the risk of dying from the treatment can be very high, so we usually only offer that for patients who are young and healthy enough to tolerate it. 12/
Instead, everything else is geared toward treating the symptoms. There are a TON of therapies around, and every institution is different. We generally start with extracorporeal photopheresis since it's the least toxic, but the list of possible options is huge! 13/
Every patient is different. Some do well for decades on ECP! Some progress and require more aggressive therapy. I've seen patient do well on low dose alemtuzumab, some cured with SCT! Everyone needs a tailored approach that balances symptom management with risk of therapy.
14/
The Comprehensive Cutaneous Lymphoma Program (CCLP) I co-direct @MGHCancerCenter is a multidisciplinary clinic with myself, oncology, pathology, and radiation oncology. This is a perfect time for multi-D care, and it's so fun to take care of these complex patients together.
15/
RECAP!
✅SS is a tumor of the circulating memory T-cells.
✅Erythroderma is classic, with keratoderma, ectropion, lymphadenopathy, and insensible losses.
✅Work up with skin biopsy, CBC/d, flow from blood.
✅Only one cure (SCT). Tailored symptom management is primary goal.
16/
Thanks for joining, & a shout out my amazing colleagues in the CCLP at MGH. Dr. Jeffrey Barnes/Dr. Salvia Jain (Onc), Dr. Chirayu Patel (Rad/Onc), the entire dermpath/hemepath group, the nurses, MAs, staff are all an amazing crew to work with!
Until next time!
17/17
• • •
Missing some Tweet in this thread? You can try to
force a refresh
Hi #medtwitter and #dermtwitter! Since I'm giving a talk at the upcoming @SocietyHospMed Converge meeting, I thought I'd put together a brief #tweetorial on:
DIFFERENTIATING PEMPHIGUS AND PEMPHIGOID!
Follow along for a reminder on how to tell them apart! 1/
Reminder that Pemphigus is from an antibody targeting the Desmosome - which holds skin cells (keratinocytes) together.
Pemphigoid is from an antibody targeting the Hemidesmosome, which holds keratinocytes to the basement membrane.
pc: 2/ bookdown.org/jcog196013/BS2…
So to remember:
pemphiguS (S for Superficial/higher up)
pemphigoiD (D for Deep/lower down)
This also means the clinical exam is different. Since Pemphigoid is deeper, these bullae stand tall and proud and don't droop over (see pic)! We call these TENSE bullae. 3/
If everyone could just humor me for a little, here's a #dermtwitter/#medtwitter/#pharmtwitter #tweetorial on...
AZATHIOPRINE
Did you know that dermatologists use this medication too? Read on to see all the ins and outs of safety and dosing, from a #dermatology point of view! 1/
Did you notice those two rings above? That's how it works.
Azathioprine is a purine (see figure) analogue, so it gets in the way of RNA/DNA synthesis (making transcription and replication and all that downstream goodness more difficult). 2/
And as you might imagine, cells that are rapidly dividing (like your immune cells) would be affected more by this purine disruption.
But it's not azathioprine itself that does all the work. It has to be broken down into active metabolites and that's where it gets interesting. 3/
The spirochete Borrelia burgdorferi is the most common cause. It is transmitted via tick bite, and so, certain areas of the country have higher rates based on endemicity of the organism.
What tick classically transmits lyme?
2/
Ixodes tick is the classic vector for B burgdorferi. But remember:
The tick usually has to be attached to the patient for >36 hours to transmit and cause Lyme disease.
Can you identify all these types of ticks and pick out which one is Ixodes?
We're seeing more consult questions for this, and it's also garnering national attention, so let's take a brief moment in #tweetorial format to talk about:
What is Xylazine? It was created in the 70s as a veterinary anesthetic. As an analog of clonidine, it has similar effects as an alpha-2 agonist, leading to sedation, anesthesia, and euphoria in the CNS. 2/
Recently, Xylazine has entered the drug supply, moreso in certain cities, but increasingly everywhere. It is often mixed with fentanyl as a cutting agent, and can also be used on its own. It may be called Tranq, Zombie Drug, or anestesia de caballo (horse anesthetic).
3/
Let's go back to the basics. Syphilis is from an infection by the bacterium Treponema pallidum. Usually spread by sexual means, syphilis has three main stages of disease.
Primary infection usually presents as a papule that turns into a painless ulcer called a chancre. 2/
Time from inoculation to chancre usually is 10-90 days (21 days is most typical).
There is a rare variant where the patient can get many smaller ulcerations, which is called Follman balanitis. 3/
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?
1/
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/