Opioid-Induced Leukoencephalopathies: A Report of Two Cases.

Case Rep Neurol

Department of Radiology and Nuclear Medicine, Hospital South West Jutland, Esbjerg, Denmark.

Published: February 2022

Acute toxic leukoencephalopathy (ATL) and delayed post-hypoxic leukoencephalopathy (DPHL) are two possible adverse entities related to opioid intoxication (OI), each having a distinct clinical course. While ATL shows a monophasic course with gradual neurological deterioration, DPHL has a distinct biphasic course. We report a case of ATL along with a case of DPHL happening in young male patients with OI, including their clinical courses as well as imaging characteristics with comparable time intervals. Initially, both leukoencephalopathies typically show magnetic resonance imaging findings with confluent and symmetric white matter (WM) abnormalities in the periventricular regions on T2 and fluid-attenuated inversion recovery images along with restricted diffusion on diffusion-weighted imaging. The DPHL patient however also presented with WM cystic substance loss in the deterioration phase, several weeks after hospital admission, which was previously described in a case of DPHL. Interestingly, similar WM changes have recently been observed in virus-associated necrotizing disseminated acute leukoencephalopathy in patients with coronavirus disease 2019 which may suggest a common pathophysiological mechanism. Knowing the distinct imaging features of ATL and DPHL along with their typical clinical courses can provide a faster and more reliable differentiation between these two entities.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832237PMC
http://dx.doi.org/10.1159/000521410DOI Listing

Publication Analysis

Top Keywords

case dphl
8
clinical courses
8
dphl
6
opioid-induced leukoencephalopathies
4
leukoencephalopathies report
4
report cases
4
cases acute
4
acute toxic
4
toxic leukoencephalopathy
4
atl
4

Similar Publications

Article Synopsis
  • Delayed post-hypoxic leukoencephalopathy (DPHL) occurs after a patient recovers from a hypoxic event, such as carbon monoxide poisoning or drug overdose, but then experiences neurological decline, often with a lucid interval of one to four weeks.
  • A case of a 70-year-old woman who developed cognitive decline and movement disorders after an opium overdose highlighted new symptoms associated with DPHL, including chorea and apraxia, alongside characteristic MRI findings.
  • The detection of 14-3-3 protein in her cerebrospinal fluid suggests it may serve as a valuable biomarker for DPHL, indicating the need for more research on its role in diagnosis and prognosis.
View Article and Find Full Text PDF

Akinetic mutism and gait disturbance in a patient with delayed post-hypoxic leukoencephalopathy.

Neurocase

February 2024

Department of Physical Therapy, College of Health Science, Eulji University, Sungnam-si, Republic of Korea.

We report on a patient with delayed post-hypoxic leukoencephalopathy (DPHL) who showed akinetic mutism and gait disturbance, neural injuries that were demonstrated on diffusion tensor tractography (DTT). A patient was exposed to carbon monoxide (CO) and rapidly recovered; however, two weeks after onset, he began to show cognitive impairment and gait disturbance. At six weeks after CO exposure, he showed akinetic mutism and gait inability.

View Article and Find Full Text PDF

This is the case of a 26-year-old male who developed Anton Babinski syndrome (ABS), quadriplegia, and delayed post-hypoxic leukoencephalopathy (DPHL) after an opioid overdose. He exhibited cortical blindness, visual anosognosia, and confabulation upon awakening. Several days later, he experienced acute psychosis and agitation.

View Article and Find Full Text PDF

Delayed post-hypoxic leukoencephalopathy (DPHL) is a poorly recognized syndrome characterized by neuropsychiatric symptoms following recovery from an acute hypoxic episode. Although most cases are related to carbon monoxide poisoning, some have been linked to excessive opioid use. Opioid intoxication has recently become known for manifesting the characteristic imaging findings involving cerebellar, hippocampal, and basal nuclei transient edema with restricted diffusion (CHANTER) syndrome.

View Article and Find Full Text PDF

We report a neuropsychological evaluation for a 39-year-old, right-handed, white female who 8 years ago developed delayed post-hypoxic leukoencephalopathy (DPHL), a rare demyelinating syndrome, two-weeks following an anoxic brain injury due to an overdose from benzodiazepines. An extensive record review documenting her medical timeline and treatment over the last 8 years was conducted using the available EMR system, which also included both EEG and neuroimaging data. Eight years post injury, a comprehensive neuropsychological battery was administered with corrected normative data for age, race, education, and other demographic factors when available.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!