在使用娱乐性药物期间检测到遗传性神经病变与压力性麻痹的易感性。

IF 0.7 Q4 CLINICAL NEUROLOGY Neurohospitalist Pub Date : 2023-10-01 Epub Date: 2023-05-12 DOI:10.1177/19418744231174396
Giovanni Castellucci, Michelle Figueroa, Lalitha Sivaswamy
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引用次数: 0

摘要

背景:一氧化二氮(N2O)在过去几年中一直是一种越来越受欢迎的娱乐药物。虐待会导致严重的神经系统并发症,甚至致命的后果。目的:我们报告一例青少年慢性一氧化氮滥用,表现为快速进行性混合感觉和运动性多发性神经病。结果:初步诊断排除了电解质紊乱、重金属中毒、自身免疫性神经病、肌病、血液系统疾病和甲状腺疾病。在进一步询问中,患者报告吸入一氧化二氮8个月,通常被称为“鞭虫”。随后的测试显示维生素B12含量低,同型半胱氨酸水平升高。最终的遗传测试表明,编码外周髓磷脂蛋白22(PMP22)的基因存在杂合缺失,这与压力性麻痹遗传性神经病(HNPP)的诊断一致。结论:神经和遗传发现与吸入氧化亚氮的时间线的相关性表明,她的症状是多因素的病因,N2O是电诊断研究中检测到的轴突变性和脱髓鞘的触发因素。
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Hereditary Neuropathy With Liability to Pressure Palsy Detected During the Use of Recreational Drugs.

Background: Nitrous oxide (N2O) has been an increasingly popular recreational drug over the past few years. Abuse is associated with severe neurological complications and even fatal outcomes. Purpose: Here we present a case of chronic nitric oxide abuse in a teenager presenting with rapidly progressive mixed sensory and motor polyneuropathy. Results: The initial diagnostic workup excluded electrolyte derangement, heavy metal intoxication, autoimmune neuropathy, myopathy, hematological disorders, and thyroid disease. On further questioning, patient reported 8-months of inhalation of nitrous oxide, commonly known as "whippets". Subsequent tests revealed low Vitamin B12 and elevated homocysteine level. Eventual genetic test demonstrated a heterozygous deletion in the gene that encodes the peripheral myelin protein 22 (PMP22), consistent with a diagnosis of Hereditary Neuropathy with Liability to Pressure Palsies (HNPP). Conclusion: The association of neurologic and genetic findings with the timeline of nitrous oxide inhalation suggests a multifactorial etiology of her symptoms, with the N2O acting as a trigger to the axonal degeneration and demyelination detected on electrodiagnostic studies.

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来源期刊
Neurohospitalist
Neurohospitalist CLINICAL NEUROLOGY-
CiteScore
1.60
自引率
0.00%
发文量
108
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