Sebastian López

885 posts

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Sebastian López

Sebastian López

@mdsebaslopez

Autoimmune Neurology | Neuroimmunology | Neurohospitalist at @Mayoclinic | Personal account

Pontevedra beach Katılım Mart 2011
822 Takip Edilen1.9K Takipçiler
Sebastian López
Sebastian López@mdsebaslopez·
I am biased because I see these patients in a neuroimmunology clinic, where many progressive myelopathies are labeled as “transverse myelitis,” and delayed diagnosis is unfortunately common among them. Typically a man >50 with slowly progressive myelopathy over months. Radicular pain is a frequent initial symptom, often presenting as chronic, insidious low back pain. Prior spine surgery is not uncommon. Symptoms may worsen with steroids or show only transient improvement. Stepwise decline with exertion/Valsalva,early gait impairment and neurogenic bladder/bowel dysfunction. Important pitfalls: absence of obvious flow voids on MRI does not exclude the diagnosis. CSF is often abnormal (elevated RBCs protein common), but pleocytosis is uncommon. A single spinal angiogram may be negative, some patients require repeat, highly selective angiography, and occasionally surgical exploration to localize and treat the fistula. Any unexplained thoracic myelopathy extending to the conus should prompt a thorough evaluation for a spinal dural AV fistula.
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Daniel Gewolb, MD
Daniel Gewolb, MD@daniel_gewolb·
🔷CLINICAL: ▶️Chronic progressive myelopathic symptoms in older adults ▶️Males:Females (~5:1) ▶️Bleeding is uncommon ⭐️Clinicians please share clinical pearls 🙏 🔷IMAGING: ▶️Serpiginous perimedullary flow voids usually dorsal to the cord ▶️Cord edema usually beginning caudally near the conus from venous hypertension and UNRELATED IN LOCATION TO THE FISTULA ▶️Patchy ill-defined enhancement ▶️When diagnoses are delayed: 80% enhance, 96% have edema, 96% have flow voids ▶️The fistulous connection and early filling radicular vein can be localized on first-pass MRA or TR-MRA
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Elia Sechi
Elia Sechi@EliaSechi·
In our recent study, the "Insular Knife Cut" Sign had 99.3% specificity for HSV encephalitis and was often detectable early after symptoms onset on brain MRI. An ominous sign not to miss in patients with suspected encephalitis of new onset!!! doi.org/10.1111/ene.70…
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Eoin Flanagan
Eoin Flanagan@EoinFlanagan14·
Happy to share Syc-Mazurek et al study of attack & remission MRI in #MOGAD vs #MS ➡️ Resolution of 1 lesion predicts #MOGAD and disappearance of ≥2 lesions separates #MOGAD completely from #MS ➡️ MRI 1 yr post #MOGAD brain/spine attack may aid diagnosis👇jnnp.bmj.com/content/early/…
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Marcus Pinto, MD, MS
Marcus Pinto, MD, MS@MarcusVPinto·
Dear Neurology Residents Starting in the ED Next Month, You will frequently encounter “?GBS” or “GBS rule out” consults. Please remember to carry your reflex hammer, save this post for future reference, and read the open-access review that I share ⬇️. 🤓 Since you won’t have much time for history taking, make sure to ask about important details such as falls, the use of gait aids, the ability to climb stairs, difficulty walking, using zippers, and washing their hair. These activities can help you gather an accurate timeline. I also suggest asking when they last felt like their usual selves, as this can help pinpoint when the symptoms began, along with their prior level of disability, which is crucial. Don't forget to ask about potential triggers, including recent vaccinations, infections, surgery, and trauma. The following physical examination features make GBS very unlikely and may assist you in “ruling it out”: - A sensory level - Unilateral weakness - Markedly asymmetric weakness (excluding cranial nerves) - Weakness confined to either the upper or lower limbs - Normal (or preserved) ankle reflexes - Fever or skin rash - Normal gait GBS is the most common cause of ascending weakness and paresthesias. So, if history suggests it, the patient is unable to walk, the weakness is symmetric, and the reflexes are reduced/absent, please admit the patient and start IVIg overnight. Time is nerve! 😅
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Eoin Flanagan
Eoin Flanagan@EoinFlanagan14·
Happy to share @albertaboseif et al multicenter study showing 4% of #MOGAD with meningitis ➡️ Frequent misdiagnosis as infection ➡️ Updates in criteria could incorporate this phenotype ➡️ Path had meningeal T & B cells, microglia & cortical myelin loss👇 jamanetwork.com/journals/jaman…
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Sebastian López
Sebastian López@mdsebaslopez·
Great time celebrating Dr. Newman — our exceptional fellow in Autoimmune Neurology!
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Dr. Brandon Beaber
Dr. Brandon Beaber@Brandon_Beaber·
MRI findings of genetic diseases often misdiagnosed as MS. A-D LHON B CADASIL. D CANVAS. E Krabbe disease F Cobalamin C disease. G polymerase gamma gene disease. H Alexander J/K CADASIL L Spastic paraplegia 5 with diffuse leukoencephalopathy pubmed.ncbi.nlm.nih.gov/40446704/
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Michelle Monje 🟦
Michelle Monje 🟦@michelle_monje·
Delighted to share our new study, led by @annacgeraghty and @LehiAcosta , uncovering the cellular dysregulation underpinning cognitive impairment after CAR T cell therapy and a strategy to rescue this cellular and cognitive dysfunction in mice. 1/ cell.com/cell/fulltext/…
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Eoin Flanagan
Eoin Flanagan@EoinFlanagan14·
Delighted to share Cacciaguerra et al study ➡️ MRI guidelines in MS recommend 2 sagittal-T2 spine images but axial is optional ➡️ Here, axial-T2 found 2x more lesions vs sagittal ➡️ Thus, future guidelines should recommend both sagittal & axial images👇 #citeas" target="_blank" rel="nofollow noopener">link.springer.com/article/10.100…
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Sebastian López
Sebastian López@mdsebaslopez·
Thanks for sharing our work on ‘CNS Tractopathies’ so nicely. This is often clinically challenging, given the broad differential diagnosis. We hope this article helps neurologists and neuroradiologists narrow down the diagnosis!
Lea Alhilali, MD@teachplaygrub

1/Do you have trouble keeping track of all the tractopathies? Wish you knew mo’ about mo’ tor neuron diseases? Read on for what you need to know in this months Radiographics review of motor neuron diseases! doi.org/10.1148/rg.240… @cookyscan1 @RadG_editor @RadioGraphics

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Matteo Gastaldi
Matteo Gastaldi@MGastaldi85·
neurology.org/doi/10.1212/NX… Proud to share @StefanoMascio91 latest work on PLP1 antibodies in demyelinating diseases. PLP1 abs are mainly found in patients with non MS diseases with combined central and peripheral demyelination, but also in rare seronegative NMOSD
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