古柯碱致咽部穿孔—一例罕见的面部及颈部肺气肿合并纵隔气肿的表现

A. Herman, R. Anmolsingh, A Alappatt, Pothula Vb, Kumar Bn
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引用次数: 0

摘要

目的:颈部和面部手术肺气肿合并纵隔气肿的原因并不常见,但可能危及生命,需要在高度依赖的环境中紧急处理。我们提出一个病例继发可卡因诱导下咽穿孔,这是不容易诊断,因为病人不愿与他的可卡因使用史。当患者出现扩散性宫颈肺气肿时,临床医生应保持高度的怀疑指数,并建议一种非医源性皮下肺气肿和咽痛的处理方法。病例总结:我们报告了一个39岁的男性,表现为3天的突然严重咽痰和咳嗽,痰中有血丝。最初的胸部和颈部软组织x线片显示颈椎手术肺气肿。经进一步询问,他承认最近经常鼻腔吸入可卡因。随后的颈部和胸部CT显示广泛的皮下肺气肿可能是由于食管穿孔。这是证实胃grafin吞咽试验,显示后下咽穿孔。患者在HDU中保守治疗,口服麻醉,静脉滴注哌拉西林/他唑巴坦和克林霉素。他最初接受全肠外营养,但随后拒绝进一步静脉内营养。出院后予社区鼻胃喂养。出院后两周随访吞咽试验显示穿孔消退。在此之后,我们开发了一种算法,强调在确定调查之前进行早期稳定和彻底评估,以改善管理。结论:可卡因致咽部穿孔是一种罕见但可能危及生命的疾病,如果不及时诊断和积极的保守治疗。彻底的病史记录对于保持高度怀疑至关重要,因为可能的病理可能危及生命。多学科团队的早期介入建议也至关重要。
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Cocaine Induced Pharyngeal Perforation-an Unusual Case Presentation of Facial and Cervical Emphysema with Pneumomediastinum
Objectives: Causes of cervical and facial surgical emphysema with pneumomediastinum are uncommon but can be life threatening and need urgent management in a high dependency setting. We present a case secondary to cocaine induced hypopharyngeal perforation which was not easy to diagnose as the patient was not forthcoming with his history of cocaine use. Clinicians should maintain a high index of suspicion when patients present with spreading cervical emphysema and also suggest an algorithm for management of non-iatrogenic subcutaneous emphysema and odynophagia. Case summary: We presented a case report of a 39 year old man presented with three days history of sudden severe odynophagia and coughing frothy blood stained sputum. Initial chest and neck soft tissue radiograph revealed cervical surgical emphysema. After further questioning, he admitted to recent regular cocaine nasal inhalation. Subsequent CT neck and thorax showed extensive subcutaneous emphysema likely due to an esophageal perforation. This was confirmed by gastrografin swallow test, which demonstrated a posterior hypopharyngeal perforation. The patient was managed conservatively in a HDU by keeping him nil by mouth and treatment with IV Piperacillin/Tazobactam and Clindamycin. He initially received total parenteral nutrition but subsequently refused further intravenous nutrition. He was discharged with nasogastric feeding in the community. Follow-up swallow test two weeks following discharge showed resolution of the perforation. Subsequent to this, we developed an algorithm with an emphasis on early stabilisation and thorough assessment prior to definitive investigation to improve management. Conclusion: Cocaine induced pharyngeal perforation is a rare but potentially life-threatening condition if left undiagnosed and without prompt and aggressive conservative treatment. Thorough history taking is vital with maintenance of high level of suspicion as the likely pathologies can be life threatening. Early involvement of multidisciplinary team advice is also critical.
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