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Cannabis: the next villain on the lung cancer battlefield?
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Emphysema and secondary pneumothorax in young adults smoking cannabis.年轻大麻吸食者的肺气肿和继发性气胸
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5
Effects of cannabis on pulmonary structure, function and symptoms.大麻对肺部结构、功能及症状的影响。
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一例高剂量吸食大麻导致的严重多系统功能障碍

Severe multisystem dysfunction in a case of high level exposure to smoked cannabis.

作者信息

Reece Albert Stuart

机构信息

University of Queensland, Medical School, 39 Gladstone Road, Highgate Hill, Brisbane, Queensland, 4101, Australia.

出版信息

BMJ Case Rep. 2009;2009. doi: 10.1136/bcr.08.2008.0798. Epub 2009 Sep 2.

DOI:10.1136/bcr.08.2008.0798
PMID:21887157
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3029389/
Abstract

Cannabis use is common, controversial and its clinical toxicology is likely under-recognised. A 56-year-old man presented with disabling shortness of breath. He smoked up to 7 g cannabis daily for 25 years (maximum 63 875 g) plus large amounts of hashish oil. Chest x ray suggested giant bullae. CT of the chest revealed over 40 bullae, the largest being 11 cm in diameter. Osteoporosis with multiple vertebral crush fractures was noted on plain films and bone densitometry (t=-3.19). His dental health was poor. Hypertension, complicated by a large occipital stroke was shown by CT of the brain, and increased vascular age (69.8 years) found by pulse wave analysis. The case is significant as it indicates the potential severity of cannabis lung damage and suggests that significant cannabis exposure may cause osteoporosis and accelerated vascular ageing. The association of alveolar destruction, bone lysis and destruction of arterial elastic laminae suggest possible underlying mechanisms such as tissue proteinase activation, immunomodulation or stem cell impairment.

摘要

大麻使用很常见且存在争议,其临床毒理学可能未得到充分认识。一名56岁男性因严重呼吸困难就诊。他每天吸食多达7克大麻,持续25年(总量达63875克),此外还吸食大量大麻油。胸部X光显示有巨大肺大疱。胸部CT显示有40多个肺大疱,最大直径达11厘米。X线平片和骨密度测量显示有骨质疏松并伴有多个椎体压缩性骨折(t=-3.19)。他的口腔健康状况很差。脑部CT显示患有高血压并伴有大面积枕叶中风,脉搏波分析显示血管年龄增加(69.8岁)。该病例意义重大,因为它表明了大麻对肺部损害的潜在严重性,并提示大量接触大麻可能导致骨质疏松和血管加速老化。肺泡破坏、骨质溶解和动脉弹性膜破坏之间的关联提示了可能的潜在机制,如组织蛋白酶激活、免疫调节或干细胞损伤。