Toxic Leukoencephalopathy Presenting as Lethal Catatonia.

J Addict Med

Department of Psychiatry, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands (AMJvE, AF, JGEJ, AFAS); Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands (BSH, RAJE); and Department of Radiology, Radboud University Medical Center, Nijmegen, the Netherlands (SCAS).

Published: June 2020

Introduction: Catatonia is a syndrome that can present in different forms and can occur in multiple psychiatric and somatic conditions. This case report describes lethal catatonia caused by delayed toxic leukoencephalopathy after excessive use of cocaine and methadone. The characteristic radiographic imaging and biphasic course are discussed.

Case Report: A 54-year-old woman was presented unconsciously at the emergency department after intoxication with methadone and cocaine. After initial recovery, her condition deteriorated unexpectedly, resulting in lethal catatonia. Magnetic resonance imaging (MRI) showed hyperintense white matter abnormalities and diffusion restriction, evident for leukoencephalopathy.

Discussion: Catatonia can develop in multiple psychiatric and somatic diseases, including toxic leukoencephalopathy. A biphasic course and specific MRI findings are characteristics for delayed toxic leukoencephalopathy, due to intoxication with drugs.

Download full-text PDF

Source
http://dx.doi.org/10.1097/ADM.0000000000000470DOI Listing

Publication Analysis

Top Keywords

toxic leukoencephalopathy
16
lethal catatonia
12
multiple psychiatric
8
psychiatric somatic
8
delayed toxic
8
biphasic course
8
catatonia
5
toxic
4
leukoencephalopathy presenting
4
presenting lethal
4

Similar Publications

: Recent advances in childhood acute lymphoblastic leukemia (ALL) and lymphoblastic lymphoma (LL) management provide higher survival rates at the cost of increased toxicities. Acute neurotoxicity affects up to 10% of patients, requiring rapid recognition and treatment. : A retrospective observational study was performed to determine the frequency, clinical manifestations, radiological characteristics, treatment options and outcome of acute neurological adverse events in pediatric patients with lymphoid malignancies at the Department of Oncology and Hematology, Children's Hospital Zagreb, Croatia.

View Article and Find Full Text PDF

Background: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is one of the most common inherited cerebral small vessel diseases caused by the NOTCH3 gene mutation. This mutation leads to the accumulation of NOTCH3 extracellular domain protein (NOTCH3) into the cerebral arterioles, causing recurrent stroke, white matter lesions, and cognitive impairment. With the development of gene sequencing technology, cysteine-sparing mutations can also cause CADASIL disease, however, the pathogenicity and pathogenic mechanisms of cysteine-sparing mutations remain controversial.

View Article and Find Full Text PDF

Background: The defining characteristic of posterior reversible encephalopathy syndrome (PRES) is a reversible, predominantly vasogenic edema of the white matter, particularly affecting the parenchyma supplied by the posterior circulation. PRES is most commonly associated with hypertension. We present a case series of seven normotensive patients diagnosed with cancer who had posterior reversible encephalopathy syndrome.

View Article and Find Full Text PDF

Characterization of gallbladder disease in metachromatic leukodystrophy across the lifespan.

Mol Genet Metab

January 2025

The Children's Hospital of Philadelphia, Neurology, 3401 Civic Center Blvd, Philadelphia 19104, PA, USA. Electronic address:

Metachromatic leukodystrophy (MLD) is a progressive demyelinating disorder resulting from the toxic accumulation of sulfatides. The stereotyped neurodegeneration of MLD is well understood, and cases are categorized into subtypes by age at neurologic onset: late infantile (LI), juvenile (J), and adult. The systemic burden of disease, such as gallbladder involvement, however, is less well characterized.

View Article and Find Full Text PDF

Linezolid induced acute toxic leukoencephalopathy and severe thrombocytopenia presenting as stroke mimic-a case report.

Oxf Med Case Reports

December 2024

Haematology, Colchester Hospital, East Suffolk and North Essex NHS Foundation Trust, Turner Road, Colchester, United Kingdom.

Article Synopsis
  • A 67-year-old woman was admitted for right-sided weakness, shaking, lethargy, and loss of appetite after completing treatment for a diabetic foot infection.
  • MRI results revealed changes in the deep white matter of her brain, potentially indicating an ischemic stroke, alongside symptoms of verbal dysfluency and visual disturbances.
  • After a decline in her condition and a drop in blood counts, she was diagnosed with Linezolid-induced Acute Toxic Leukoencephalopathy and thrombocytopenia based on her clinical presentation and imaging.
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!