Delayed post-hypoxic leukoencephalopathy

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DSS 2013-Case 2
Declan McGuone, Jeremy Schmahmann,
E. Tessa Hedley-Whyte, Matthew P. Frosch
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Disclosures
NONE
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Clinical History
• 69 yo pain & stiffness 2 days after neck lipectomy
• No sx of infection or neurologic symptoms
• Hydromorphone (1.5mg + 1mg) & diphenhydramine
(25+25 mg)
• Admitted. Next AM unresponsive, hypotensive &
hypoxic. Resuscitated and receives Narcan
• Discharged home at baseline 3 days later
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Clinical History, cont.
• 3 WKS :
– Behavioral, memory &
attention deficits appeared.
– Over next 72 hrs rapid
decline in mental status
with progressive akinesia,
mutism & rigidity
• Lab investigations
– Unremarkable
T2/FLAIR
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Clinical History
• 3 MOS : she was alert, responsive, followed simple
commands.
• 6-9 MOS: fluent speech, paranoid & delusional with
impaired visuo-spatial, memory encoding, exec. &
behavioral functions.
• Death 2 years following presentation
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1300g
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Discussion
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Neurofilament
GFAP
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CD45
CD68
CD45
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Diagnosis
Delayed post-hypoxic leukoencephalopathy
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Delayed post-hypoxic leukoencephalopathy
• A rare complication of prolonged cerebral hypoxia
• The classic clinical presentation is biphasic – patients recover within
24hours of a prolonged hypoxic injury and return to baseline before
developing a sudden onset neuropsychiatric syndrome within 1-3
weeks
• Exact incidence is not known
• Etiology of insults reported to cause DPHL is heterogeneous (e.g.
anoxic anoxia, anemic anoxia and ischemic anoxia)
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Delayed post-hypoxic leukoencephalopathy
• Two clinical phenotypes:
– Parkinsonism
• Rigidity, tremor, masked facies. dystonic posturing, agitation,
apathy, hallucinations, odd behavior, impaired cognition,
emotional lability
– Akinetic mutism
• Apathy, functional incontinence, pathologic laughter or
crying,
• Examination:
– Frontal release signs
– CST signs (hyperreflexia, Babinski)
– Frontal-executive dysfunction
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Neuropathology
• Severe diffuse hemispheric
demyelination (sparing of U-fibers)
• Morphologically normal oligodendroglia
• No vacuolar change (as sometimes
seen with inhaled heroin)
• Preserved neocortical and
hippocampal architecture
•Elevated CSF myelin basic protein
(marker of acute widespread
demyelination)
Plum and Posner, Archives internal medicine, 1962
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Mechanism
• Unknown but likely multifactorial
• ? Mitochondrial dysfunction
– DPHL can be reproduced in animals using potassium cyanide to
impair cytochrome c (Shprecher D, Mehta L, et al. Neurorehabilitation, 2010)
• ? Reduced cerebral blood flow (DPHL more prevalent and more
severe in older patients with cerebrovascular disease)
• ? Pseudodeficiency of Arylsulfatase A (Gottfried JA, Mayer SA et al. Neurology
1997)
• ? Delayed oligodendroglial apoptosis (Chu K, Jung KH et al. Eur Neurol 2004)
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References
[1] Plum F, Posner JB, et al. Delayed neurological deterioration after
anoxia. Arch Intern Med, 1962
[2] Shprecher D, Mehta L. The syndrome of delayed post-hypoxic
leukoencephalopathy. Neurorehabilitation, 2010.
[3] Shprecher D, Flanigan K et al. Clinical and diagnostic features of
delayed hypoxic leukeoncephalopathy. J Neuropsychitary Clin
Neurosci, 2008
[4] Choi IS. Delayed neurologic sequelae in carbon monoxide
intoxication. Arch Neurol, 1983
[5] Gottfried JA, et al. Delayed posthypoxic demyelination. Association
with arylsulfatase A deficiency and lactic acidosis on proton MR
spectroscopy. Neurology 1997.
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