Case 1 SF 41 y/o woman with no PMHx p/w blurry vision and headache worsening x few weeks. No meds,...
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Transcript of Case 1 SF 41 y/o woman with no PMHx p/w blurry vision and headache worsening x few weeks. No meds,...
![Page 1: Case 1 SF 41 y/o woman with no PMHx p/w blurry vision and headache worsening x few weeks. No meds, no toxic habits. PE: Afeb VSS. Bilateral lid swelling.](https://reader033.fdocuments.us/reader033/viewer/2022051516/56649d965503460f94a7fc7d/html5/thumbnails/1.jpg)
Case 1 SF
• 41 y/o woman with no PMHx p/w blurry vision and headache worsening x few weeks. No meds, no toxic habits.
• PE: Afeb VSS. Bilateral lid swelling. • Neuro exam: MSE with mild cognitive
slowing and diminished attention, otherwise normal. CN: diminished VA with disc swelling b/l.
• Motor/sensory/cerebellar intact.
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Other w/u
• LP: elevated opening pressure, CSF lymphocytic pleocytosis (60-80), prt 80
• Serum ACE: ~65
• CSF ACE: ~20
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Clinical course
• Progressive cognitive decline, recurring bouts of aseptic meningitis with visual blurring partially responsive to IV steroids.
• Poor compliance pulse Cytoxan
• Later developed poor vision d/t glaucoma and b/l optic neuritis
• Panhypopituitarism
• Dementia
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Case 2 RC
• 44 y/o man with hx of CVA and behavioral problems, p/w AMS and difficulty walking. Prior CVA admitted at Montefiore 2005, p/w . W/u revealed basal ganglia and cerebellar calcification on CT scan, acute R midbrain/thalamic infarct on MRI. Cause of stroke in young uncertain, however pt found to be ANA+.
• Meds:
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• PE: Afeb VSS
Neuro: MSE: alert, Ox2, dim attention, STM 1/3.
CN: dysarthric, otherwise intact
Motor: increased tone in legs, full strength, mild incoordination on FTN,
DTRs: hyperactive
Gait: spastic/ataxic
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Imaging
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Other w/u
• ESR 120
• Creatinine 2-3 (prior baseline 1-1.5)
• ANA and dsDNA+
• Anti-cardiolipin Ab+
• MRI spinal cord: no significant abnl
• Cerebral angiogram: possibly slight medium vessel irregularity c/w vasculopathy
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Clinical course
• IV steroids
• IVIG
• Mycophenolate
• Warfarin
• Worsening dementia and paraparesis
• D/c to SNF
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CNS Inflammatory Disease
• Primary, recurrent demyelinating diseases: MS, Neuromyelitis Optica (NMO, Devic’s Dx)
• Mono-phasic demyelinating diseases: Acute disseminated encephalomyelitis (ADEM), acute hemorrhagic leukoencephalitis (AHLE), transverse myelitis (TM), optic neuritis (ON); often these are para-infectious
• CNS involvement with systemic (clinical or sub-clinical) auto-immune disease; includes primary and secondary CNS vasculitis
• Paraneoplastic dx• Immune reconstitution inflammatory syndrome (IRIS) • CNS infections (discussed in other lecture)
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Systemic inflammatory conditions with frequent neurological manifestations
• SLE neuropsychiatric manifestations• Sjogren’s• Sarcoid• Anti-phospholipid Ab syndrome (1º or 2º)• Rheumatoid arthritis: PNS• Vasculitis: large or small vessel• Large: Giant cell arteritis: CN>CVA• Small: Wegener’s, polyarteritis nodosum: mononeuritis
multiplex > CN >>CNS • Paraneoplastic syndromes: cerebellar dx, limbic
encephalitis, PNS
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Focal Clinical Presentation
• Focal CNS deficit (brain or brainstem): hemiparesis, hemisensory loss, hemiataxia, diplopia, vertigo, dysarthria
• Spinal cord syndrome: complete (motor/sensory/autonomic), anterior, posterior, Brown Sequard
• Cranial nerve: optic neuritis, trigeminal neuralgia, facial paresis
• Pseudo-peripheral: Lhermitte’s sign, paresthesias, pain
• Focal cognitive deficit: aphasia, apraxia, neglect
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Neuropyschiatric SLE: 19 syndromes described
Joseph (2007) Neurology
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NPSLE
• Neurological dx present in: ~50% (15-90%)• Presenting with neuro symptoms: 3-5%• NPSLE worsens prognosis• NPSLE can occur without systemic flare• Lab abnl: ESR elevated 50%, ANA+ 85%,
dsDNA+ 72%, anti-phospholipid Ab 30%, complement low during flare 44%, ribosomal P Ab and C3A frequently elevated prior to/during flare.
• APS associated with NPSLE, CVA, other focal dx
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Neuro testing in NPSLE
• CSF abnl: 20-40% (lymphocytic pleocytosis, elevated prt, OCB each present in ~20%).
• EEG abnl: up to 80% abnl, mostly non-specific changes but some with epileptogenic focus.
• EMG/NCS: high% abnl in symptomatic PNS dx
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Neuroimaging
• Brain MRI: abnl in 20-70%; most common findings are multifocal small white matter hyperintensities and atrophy; stroke in < 20%; lower % show basal ganglia calcification, reversible leukoencephalopathy syndrome (RPLS).
• SPECT: detects multifocal or patchy/diffuse perfusion deficits in 50-90%
• MR spectroscopy: abnl in ? 20-50%
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MRI abnl in NPSLE ptsCsepany (2003) J Neurol
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NPSLE RxSanna 2003
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CNS LupusCsepany 2003
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Lupus RPLSMagnano 2006
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EMT with SLE, APS, complicated migraine with aphasia and RHP
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Neurosarcoidosis
• Neurological manifestations in ~10% (~20% at autopsy).
• Rarely presents with neurologic syndrome %
• Very rarely limited to NS %
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Joseph (2008) JNNP
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Spencer (2004) Sem Arthritis Rheum
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Laboratory findings in neurosarcoidosis
• CXR abnl: ~40-50% (30-80% range)
• Chest CT abnl: ~60-75% (? up to 90%)
• Gallium/PET scan abnl: 25-80%
• Serum ACE elevation: 25-75%
• CSF prt elevation: 50%
• CSF lymphocytic pleocytosis: 40%
• CSF OCB: 20-40%
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Neurosarcoid MRI abnl
• Any abnl: up to 80%
• Leptomeningeal or parenchymal enhancement: 25-50%
• White matter lesions: 30-50%
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Neurological manifestations of Sjogren’s syndrome
• Common disorder, affecting ~2-3% of adults.
• Neurological dx present in 5-60%.
• CNS and PNS dx both common.
• Neurological symptoms occur prior to diagnosis in 80-90% of patients.
• Sicca symptoms present in <50% at presentation.
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PNS Sjogren’sMori (2005) Brain
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MRI, path, and sweat testing in Sjogren’s sensory neuropathy (Mori 2005)
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Lab abnl in Neuro-Sjogren’s
• SSA/SSB+: 45%
• Schirmer’s test abnl: 90%
• Salivary scintography abnl: 65%
• Lip bx abnl: 95%
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References
• SLE: • Joseph (2008) JNNP• Sanna (2003) Lupus• Csepany et al (2003) J Neurol• Sjogren’s: • Mori (2005) Brain • Delalande (2004) Medicine• Soliotis (1999) Ann Rheum Dis• Sarcoid:• Joseph (2008) JNNP
• Joseph (2007) Practical neurology
• Spencer (2004) Sem Arthritis Rheum
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NeurosarcoidSpenser 2004
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CNS Sjogren’s