大麻素呕吐综合征并发纵隔气肿:对儿科外科医生的启示。

Clinical surgery journal Pub Date : 2022-01-01 Epub Date: 2022-07-31
Greg Klazura, Joseph R Geraghty, Marko Rojnica, Thomas Sims, Nathaniel Koo, Thom Lobe
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引用次数: 0

摘要

背景:大麻素剧吐综合征(Cannabinoid Hyperemesis Syndrome, CHS)是一种周期性呕吐综合征,其特征是每隔几周或几个月发生一次发作性呕吐,与长期和频繁使用大剂量大麻有关。在过去的十年中,儿科人群中CHS的报道越来越多,并且可能导致危及生命的并发症,如纵隔气肿,这需要仔细考虑手术干预。病例介绍:一名17岁女性,无明显既往病史,因腹痛、恶心和呕吐24小时就诊于急诊科。她有四次黄绿色呕吐,接着是干呕。她还抱怨胸部和背部疼痛,深度吸气时更严重。根据进一步的病史,患者报告在本次发作前6个月出现过类似的腹痛和反复呕吐。她每天至少吸一次大麻,过去两年一直如此。胸片示前后窗及前纵隔轻度异常透光,符合少量纵隔气肿,无其他急性胸内异常。随后的胸部计算机断层扫描显示前后纵隔内多处空气病灶,一直向上延伸至胸入口。没有造影剂外渗的证据;但不能排除小的食管穿孔。给予无明显造影剂外渗的无并发症纵隔气肿患者,给予哌拉西林-他唑巴坦、甲硝唑和米卡芬宁进行微生物预防治疗;氢吗啡酮用于疼痛控制;还有泮托拉唑,昂丹司琼和异丙嗪。通过全肠外营养提供营养。我们密切监测患者是否有隐匿性食管穿孔的迹象,但未发现任何迹象。在住院的第8天,她被推进到软性饮食,第9天开始吃固体食物,此时停用抗生素,患者随后出院。结论:由于大麻使用的流行率上升,CHS在儿科环境中越来越常见。CHS和可能危及生命的并发症(如纵隔气肿)的处理应慎重考虑。纵隔气肿可能是更险恶的病理如食管穿孔的先兆,这可能需要紧急手术干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cannabinoid Hyperemesis Syndrome Complicated by Pneumomediastinum: Implications for Pediatric Surgeons.

Cannabinoid Hyperemesis Syndrome Complicated by Pneumomediastinum: Implications for Pediatric Surgeons.

Cannabinoid Hyperemesis Syndrome Complicated by Pneumomediastinum: Implications for Pediatric Surgeons.

Background: Cannabinoid Hyperemesis Syndrome (CHS) is a form of cyclic vomiting syndrome characterized by episodic vomiting occurring every few weeks or months and is associated with prolonged and frequent use of high-dose cannabis. CHS in the pediatric population has been increasingly reported over the last decade and can lead to life-threatening complications such as pneumomediastinum, which warrant careful consideration for surgical intervention.

Case presentation: A 17-year-old female with no significant past medical history presented to the emergency department with abdominal pain, nausea, and vomiting for 24 hours. She had four episodes of green-yellow emesis followed by dry heaves. She also complained of chest and back pain, worse with deep inspiration. Upon further history, the patient reported a similar episode of abdominal pain and repetitive vomiting six months prior to the current episode. She smoked cannabis at least once daily and has done so for the past two years. Chest X-ray revealed a subtle abnormal lucency along the anteroposterior window and anterior mediastinum, consistent with a small amount of pneumomediastinum without any other acute intrathoracic abnormalities. Follow-up chest computed tomography with contrast showed multiple foci of air within the anterior and posterior mediastinum tracking up to the thoracic inlet. There was no evidence of contrast extravasation; however, small esophageal perforation could not be excluded. Given uncomplicated pneumomediastinum without frank contrast extravasation, the patient was treated medically with piperacillin-tazobactam, metronidazole, and micafungin for microbial prophylaxis; hydromorphone for pain control; as well as with pantoprazole, ondansetron, and promethazine. Nutrition was provided via total parenteral nutrition. The patient was intensely monitored for signs of occult esophageal perforation, but none were detected. She was advanced to a soft diet on hospital day eight, solid food diet on day nine, at which point antibiotics were discontinued, and the patient was subsequently discharged.

Conclusion: CHS in an increasingly common disorder encountered in the pediatric setting due to rising prevalence of cannabis use. The management of CHS and potentially life-threatening complications such as pneumomediastinum should be given careful consideration. Pneumomediastinum can be a harbinger of more sinister pathology such as esophageal perforation, which may warrant urgent surgical intervention.

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