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Erschienen in: Clinical Neuroradiology 4/2012

01.12.2012 | Correspondence

Heroin Spongiform Leukoencephalopathy (HSLE)

verfasst von: A. G. Bach, B. Jordan, N. A. Wegener, C. Rusner, M. Kornhuber, J. Abbas, A. Surov

Erschienen in: Clinical Neuroradiology | Ausgabe 4/2012

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Abstract

Purpose

An increasing number of heroin addicts—especially young and first-time users—prefer inhaling the drug to intravenous injection. A rare complication of inhaling heroin is the development of a spongiform leukoencephalopathy (HSLE).

Methods

Pathological background, symptoms, imaging, and therapeutical options are discussed on the basis of an example case.

Results

Pathophysiologically, a dysfunction of the oligodendrocyte mitochondria is suspected. Three distinct stages based on key symptoms are defined. Patients may remain in one stage, or pass through two, or all three stages. Magnetic resonance imaging (MRI) is necessary for diagnosis. There are few therapeutical options. Antioxidants and coenzyme Q may be beneficial. The disorder is self-limiting in the majority of cases. Complications such as hydrocephalus and diffuse cerebellar swelling may, however, require neurosurgical intervention.

Conclusions

HSLE is a rare occurrence in patients with heroin abuse. The number of undetected cases in drug-related deaths may be high. Clinical appearance may be easily mistaken for withdrawal symptoms.
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Metadaten
Titel
Heroin Spongiform Leukoencephalopathy (HSLE)
verfasst von
A. G. Bach
B. Jordan
N. A. Wegener
C. Rusner
M. Kornhuber
J. Abbas
A. Surov
Publikationsdatum
01.12.2012
Verlag
Springer-Verlag
Erschienen in
Clinical Neuroradiology / Ausgabe 4/2012
Print ISSN: 1869-1439
Elektronische ISSN: 1869-1447
DOI
https://doi.org/10.1007/s00062-012-0173-y

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