Delayed posthypoxic leukoencephalopathy: a case series and review of the literature

被引:53
作者
Zamora, Carlos A. [1 ]
Nauen, David [2 ]
Hynecek, Robert [1 ]
Ilica, Ahmet T. [1 ]
Izbudak, Izlem [1 ]
Sair, Haris I. [1 ]
Gujar, Sachin K. [1 ]
Pillai, Jay J. [1 ]
机构
[1] Johns Hopkins Univ, Div Neuroradiol, Russell H Morgan Dept Radiol & Radiol Sci, Sch Med, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Dept Pathol, Sch Med, Baltimore, MD 21287 USA
来源
BRAIN AND BEHAVIOR | 2015年 / 5卷 / 08期
关键词
Hypoxia; leukoencephalopathy; MRI; myelin; white matter; CARBON-MONOXIDE INTOXICATION; POSTANOXIC ENCEPHALOPATHY; ARYLSULFATASE; DEMYELINATION; OVERDOSE; FEATURES; INJURY; INSULT; DRAGON;
D O I
10.1002/brb3.364
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
BackgroundDelayed posthypoxic leukoencephalopathy (DPHL) is a rare and underrecognized entity where patients manifest a neurological relapse after initial recovery from an acute hypoxic episode. We sought to describe the magnetic resonance imaging (MRI) findings in a group of patients with DPHL and review the available literature. MethodsRetrospective case series including patients who presented with neurological and/or psychiatric symptoms after recovery from an acute hypoxic episode. The history and clinical presentation were reviewed from the electronic medical records. MRI scans were evaluated from the picture archiving and communication system. We performed a comprehensive review of the English medical literature for prior published cases of DPHL and describe the key imaging findings that have been reported related to this condition. ResultsA total of five patients were identified, including four patients with respiratory failure due to drug overdoses from benzodiazepines, opioids, and/or barbiturates, and one patient who presented after cardiopulmonary arrest due to pulmonary embolism. All patients showed diffuse, extensive, and confluent white matter signal abnormalities including prominent restricted diffusion, extending to the subcortical white matter and respecting the U-fibers. There was no gyral edema or contrast enhancement. In one case histopathology was available, which highlighted patchy subcortical myelin loss with sparing of U-fibers and demonstrated prominent macrophage/microglial inflammation with extensive axonal damage. Of the other four patients, two were at their neurological baselines and two had persistent neurological deficits at the time of discharge. ConclusionsThe described constellation of MRI findings is highly suggestive of DPHL in the appropriate clinical setting.
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页数:12
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