Case 1 SF
-
Upload
dolan-tran -
Category
Documents
-
view
34 -
download
1
description
Transcript of Case 1 SF
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.
Other w/u
• LP: elevated opening pressure, CSF lymphocytic pleocytosis (60-80), prt 80
• Serum ACE: ~65• CSF ACE: ~20
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
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:
• PE: Afeb VSSNeuro: MSE: alert, Ox2, dim attention, STM
1/3. CN: dysarthric, otherwise intactMotor: increased tone in legs, full strength,
mild incoordination on FTN, DTRs: hyperactiveGait: spastic/ataxic
Imaging
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
Clinical course
• IV steroids• IVIG• Mycophenolate• Warfarin• Worsening dementia and paraparesis• D/c to SNF
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)
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
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
Neuropyschiatric SLE: 19 syndromes described
Joseph (2007) Neurology
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
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
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%
MRI abnl in NPSLE ptsCsepany (2003) J Neurol
NPSLE RxSanna 2003
CNS LupusCsepany 2003
Lupus RPLSMagnano 2006
EMT with SLE, APS, complicated migraine with aphasia and RHP
Neurosarcoidosis
• Neurological manifestations in ~10% (~20% at autopsy).
• Rarely presents with neurologic syndrome %
• Very rarely limited to NS %
Joseph (2008) JNNP
Spencer (2004) Sem Arthritis Rheum
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%
Neurosarcoid MRI abnl
• Any abnl: up to 80%• Leptomeningeal or parenchymal
enhancement: 25-50% • White matter lesions: 30-50%
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.
PNS Sjogren’sMori (2005) Brain
MRI, path, and sweat testing in Sjogren’s sensory neuropathy (Mori 2005)
Lab abnl in Neuro-Sjogren’s
• SSA/SSB+: 45%• Schirmer’s test abnl: 90%• Salivary scintography abnl: 65%• Lip bx abnl: 95%
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
NeurosarcoidSpenser 2004
CNS Sjogren’s