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Pneumocystis jirovecii-related spontaneous pneumothorax, pneumomediastinum and subcutaneous emphysema in a liver transplant recipient: a case report

机译:肝脏移植接受者中肺炎和皮下肺气肿的肺炎与肺炎症和皮下肺气肿:案例报告

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Pneumocystis pneumonia (PCP) is a common opportunistic infection caused by Pneumocystis jirovecii. Its incidence at 2?years or more after liver transplant (LT) is ?0.1%. PCP-related spontaneous pneumothorax and/or pneumomediastinum is rare in patients without the human immunodeficiency virus, with an incidence of 0.4-4%. A 65-year-old woman who had split-graft deceased-donor LT for primary biliary cirrhosis developed fever, dyspnea and dry coughing at 25?months after transplant. Her immunosuppressants included tacrolimus, mycophenolate mofetil, and prednisolone. PCP infection was confirmed by molecular detection of Pneumocystis jirovecii,in bronchoalveolar lavage. On day-10 trimethoprim-sulphamethoxazole, her chest X-ray showed subcutaneous emphysema bilaterally, right pneumothorax and pneumomediastinum. Computed tomography of the thorax confirmed the presence of right pneumothorax, pneumomediastinum and subcutaneous emphysema. She was managed with 7-day right-sided chest drain and a 21-day course of trimethoprim-sulphamethoxazole before discharge. Longer period of PCP prophylaxis should be considered in patients who have a higher risk compared to general LT patients. High index of clinical suspicion, prompt diagnosis and treatment with ongoing patient reassessment to detect and exclude rare, potentially fatal but treatable complications are essential, especially when clinical deterioration has developed.
机译:肺炎肺炎肺炎(PCP)是由肺炎氏菌吉罗维奇引起的常用机会主义感染。它在肝脏移植(LT)后2岁或更多的发病率<?0.1%。没有人类免疫缺陷病毒的患者,PCP相关的自发性气胸和/或肺炎患者是罕见的,发病率为0.4-4%。一位65岁的女性,对原发性胆汁肝硬化的分裂死亡人士过度捐助者发烧,呼吸困难和在25岁时干咳嗽,移植后的月份。她的免疫抑制剂包括Tacrolimus,Mycophenolate Mofetil和泼尼松龙。通过支气管肺泡灌洗,通过分子检测PnEumocystis jirovecii证实了PCP感染。在Day-10甲苯乙烯 - 磺胺嘧唑,她的胸部X射线显示皮下肺气肿,双侧,右肺和肺炎。胸部的计算机断层扫描证实了右肺,肺炎肺炎和皮下肺气肿的存在。在排出前,她用7天右侧胸腔排水管和21天的Timethechokim-Sulphamethole课程进行管理。与一般LT患者相比具有更高风险的患者,应考虑更长的PCP预防。临床怀疑指数,持续诊断和治疗随着持续的患者重新评估来检测和排除罕见,可能致命但可治疗的并发症是必不可少的,特别是当临床恶化发展时。

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