Travis Smith, DO Profile picture
Jul 14, 2020 27 tweets 33 min read Read on X
It's time for a slightly tardy #SpacedRepetition: @CPSolvers

Chat recap of the #ClinicalPearls #VirtualMorningReport

July 10th Day 91: clinicalproblemsolving.com/morning-report…
w/ @AnnKumfer @DxRxEdu @rabihmgeha
Teaching points: @sukritibanthiya

Get ready for the @fernandbteich show Image
But first, we want to acknowledge @_HarryPaul_ who gave us all something to reflect on. #MichaelHickson
washingtonpost.com/health/2020/07…

Thanks for stepping up and sharing Harry!
Let’s start with a problem representation:

A 69-y/o F w/ a PMH of sinus cancer presents from an outside hospital with night sweats that started 4 wks ago along w/ rigors, fevers, nausea, early satiety, & weightloss found to have splenomegaly, lymphopenia, & elevated ESR/CRP
Given the history of sinus cancer, did she have any radiation therapy?

We want to know if she is currently immunosuppressed?

That is a big portal of entry for various local/disseminated infection

Her location Missouri is full of fungi
Rigors are predictors of bacteremia - chills without rigors are not

Now we have some more info: subacute-chronic, progressive cough, constitutional symptoms, dysphagia, early satiety, asthenia vs weakness in background of SE USA travel and multiple courses of abx
her current inflammatory syndrome does not localize anywhere

While in the hospital she got a ton of abx without avail, doxy and cextriaxone, broadened to vanc, mero, and amp B

But now we here she likes cave spelunking, hmm

histo loves it some caves, ncbi.nlm.nih.gov/m/pubmed/37465…
let's be systematic. this could be a subacute infection (atypical bacteria/fungi/parasites/viruses), a cancer or paraneoplastic syndrome related to a cancer or an autoimmune disease

if it's autoimmune we dont have enough localizing features to define it
not to leave the infection bucket, but in the back of my mind, I'm working with radiation to the head/neck and weakness/early satiety...wondering about a central endocrinopathy

in terms of infection, she does not seem immunocompromised at least based on her story
so this leaves me with atypical mycobacteria, TB, endemic fungi, parasites less likely in the midwest

viruses: a generic EBV-CMV-HIV infection can cause this
and may not respond to any antibiotics

Remember drugs can cause inflammatory syndromes but she is on nothing special
if this is SCC of the head and neck they're generally bland in terms of paraneoplastic syndromes except for PTHrP hyperCa

does she have nocardiosis and needs TMP/SMX? hmmmm, ncbi.nlm.nih.gov/pmc/articles/P…
Adding the splenomegaly to the picture:

splenomegaly w/ inflammation --> a new cancer? (Myeloproliferative disorder? lymphoma marginal zone/follicular/DLBCL?), new infection?

Are there non-cancer cause splenomegaly other than Mono? What about leishmaniasis or erlichiosis
Also mono syndromes, babesiosis, leishmania, malaria, salmonella

Can we use the presence vs absence of splenomegaly to determine the tempo of the splenomegaly manifestation?ncbi.nlm.nih.gov/books/NBK43090…

Malaria would be unlikely this far out from her residence in SE Asia.
what was the infection prevalent in east asia?

meliodosis from burkholderia pseudomallei, cdc.gov/melioidosis/in…

Now add her normal WBC but lymphopenia:

With neg BCx, unlikely to be meliodosis. Also meliodosis patients tend to present extremely sick
Her spleen is radpidly enlarging, something is growing there rapidly

is this an aggressive lymphoma?

is this burkitt's?

is this DLBCL?
Lets give an updated PR: 69yo F w/ hx of (remote?) sinus cancer s/p surgery + RT coming with subacute inflammation, rapidly progressing splenomegaly and mild liver injury.

Has so may B symptoms, but only splenomegaly. Could consider lymphoma without LAD = intravascular lymphoma
something in the spleen is spitting interleukins++ in the blood

doesn’t seem like hemolysis given the nml direct bili, but can think about babesia as well, the American malaria, cdc.gov/ticks/tickborn…
Babesia looks almost identical to malaria on smear, & treated w/ similarly
Solid cancers are allergic to spleen,

Her increased ferritin = I have inflammation

Still's doesn't have the lipid component of HLH & there is no rash or joint pain

anything that over activates the immune system can cause some degree of "HLH"
HLH is the “Lupus” of VMR

Fernand is the pearl dropper and expert investigator we all need in our lives

Quick HScore puts 40-54% probability of HLH even without positive bone marrow biopsy

And the final dx is.....
Primary Splenic Diffuse Large B-Cell Lymphoma (DLBCL) localized to a single organ
ncbi.nlm.nih.gov/pmc/articles/P…

is very rare as it occurs in less than 1% of non-Hodgkin’s lymphomas

It is most commonly found in females and older males
Symptoms can include splenomegaly as well as left upper quadrant pain, fever and weight loss.

It can also be associated with human immunodeficiency virus (HIV), and can present with metastasis to hilar and retroperitoneal lymph nodes"

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More from @RosenelliEM

May 30, 2021
Some cool #Syphilis Pearls from an article that @k_vaishnani shared ncbi.nlm.nih.gov/pmc/articles/P… Primary syphilis first manifests into a painless chancre at the site of inoculation 1 to 6 weeks later…
Hematogenous dissemination then can occur typically 4 to 10 weeks later, giving rise to secondary syphilis. <40% of pts w/ syphilis have primary syphilis diagnosed. These “Secondary” lesions last for several weeks before spontaneously resolving. Coined “early, latent infection”
What does late infection mean? When syphilitic lesions recur after 1 year from the initial eruption, or seropositivity is detected more than 1 year after the initial eruption, it is termed late latent syphilis.
Read 5 tweets
May 29, 2021
Some optics neuritis pearls in a short #Medtweetorial 🧵…. We all know that optic neuritis is frequently associated with multiple sclerosis (MS). But optic nerve inflammation can exist from autoimmunity, infection, granulomatous disease, paraneoplastic disorders, & demyelination Image
Classical ON from MS is unilateral, moderate, painful color vision loss with an afferent pupillary defect & normal fundus examination.
In those with ON, 95% of patients showed unilateral vision loss & 92% had associated retroorbital pain that frequently worsened w/ eye movement.
Read 14 tweets
Oct 1, 2020
If you have not listened to the @CuriousClinPod most recent podcast (Episode 10: Why does metronidazole treat both bacterial and parasitic infections?) then I suggest you tune in.

curiousclinicians.com/2020/09/30/why…

I'll summarize their show notes here in short #medtweetorial
First a question:

Was metronidazole first used as an antibiotic or as an antiparasitic?
If you guessed antiparasitic, then you would be correct!

It was developed in the 1950s to treat the parasite trichomonas & then was used in the 1960s to treat other parasitic infections, like giardia and amoebiasis.
Read 14 tweets
Oct 1, 2020
When you order a serum alcohol level, what does the lab measure? An answer and a quick #Medtweetorial on false elevations in #ETOH
If you guessed NADH, you would be correct.
Most lab assays for serum alcohol utilize a reagent containing alcohol dehydrogenase & NAD+

This is used to convert all present ethanol to acetaldehyde

Thereby reducing present NAD+ to NADH.
Read 11 tweets
Sep 26, 2020
A Teal pain in the neck:

Follow along for a short #medtweetorial on #CervicalArteryDissection

or see the full handout here emboardbombs.com/s/Cervical-Art…

from @EMBoardBombs @blakebriggsMD @IltifatMD
This review will focus on spontaneous dissections, not traumatic, as well as the pathophys, risk factors, presentation, diagnosis, and management.

Cervical artery dissections are a common cause of stroke in young(<50 years )w/ some reports of up to 20% being from dissections
Much like aortic dissections, there is some loss of structure along the wall of either the internal carotid artery or vertebral artery

This allows blood to collect within the intima.

In patients <50 years old, cervical artery dissections account for 20% of ischemic strokes.
Read 24 tweets
Sep 26, 2020
Time for some #SpacedRepetition from @CPSolvers @DxRxEdu @rabihmgeha

Some chat recap #ClinicalPearls and bonus pearls from #VirtualMorningReport on Friday Sept 25th clinicalproblemsolving.com/morning-report…

Case by the brilliant @Rafameed Image
A 31-year-old M born and raised in Brazil w/ no PMH presented with a 3 mon history of worsening DOE, orthopnea, 7kg weight loss, abdominal distention, dry cough, and syncope

Base rate of disease for an ID case with @k_vaishnani and @Rafameed is very high
An interesting fact from @3owllearning : Depending on the clinical problems, the studies of disease probability for differential diagnosis often show 10 - 25% of cases are unexplained, even after careful examination and testing.
Read 17 tweets

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