Alshamam Mohsen S, Sumbly Vikram, Nso Nso, Saliaj Merjona, Gurung Dawa O
Internal Medicine, Icahn School of Medicine at Mount Sinai, Queens Hospital Center, New York, USA.
Cureus. 2021 Feb 3;13(2):e13093. doi: 10.7759/cureus.13093.
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.
海洛因诱发的白质脑病(HLE)是一种罕见但可能使人衰弱甚至有时致命的神经系统疾病。尽管通过不同途径和方式使用海洛因的情况很普遍,但据说该综合征很罕见,且大多与吸入方式有关,而非注射或吸食方式。我们回顾了相关文献,以探讨与该病症相关的最新诊断、治疗和预后措施。在此,我们报告一例35岁男性病例,该患者18天前承认有吸入海洛因行为,在过去17天里一直出现持续的神经系统症状。影像学检查结果与多个层面及不同解剖区域的广泛白质病变相符。尽管目前尚无已知的治愈HLE的方法,但患者在一定程度上从抗氧化剂治疗和身体康复中获益。