| Literature DB >> 33728116 |
Mohsen S Alshamam1, Vikram Sumbly1, Nso Nso1, Merjona Saliaj1, Dawa O Gurung1.
Abstract
Heroin-induced leukoencephalopathy (HLE) is a rare but potentially debilitating and sometimes fatal neurological disorder. Despite the widely practiced heroin use via different routes and modalities, the syndrome is said to be rare and mostly associated with inhaling rather than injecting or snorting practices. We reviewed the literature to address the latest diagnostic, therapeutic, and prognostic measures related to the condition. Here, we present a case of a 35-year-old male who admitted to inhaling heroin 18 days ago and has been experiencing ongoing neurological symptoms for the past 17 days. Imaging was consistent with extensive white matter disease at multiple levels and different anatomical regions. Although there is no known cure for HLE, the patient benefited, somewhat, from antioxidants and physical rehabilitation.Entities:
Keywords: aphasia; ataxia; chasing the dragon; heroin; leukoencephalopathy
Year: 2021 PMID: 33728116 PMCID: PMC7935071 DOI: 10.7759/cureus.13093
Source DB: PubMed Journal: Cureus ISSN: 2168-8184