Larue Madeleine, Gossett Jeffrey G, Stewart Robert D, Backer Carl L, Mavroudis Constantine, Jacobs Marshall L
Case Western Reserve University School of Medicine, Cleveland, OH, USA.
World J Pediatr Congenit Heart Surg. 2012 Jul 1;3(3):364-72. doi: 10.1177/2150135112438107.
Plastic bronchitis is a rare, life-threatening condition characterized by the formation of mucofibrinous casts within the pulmonary bronchi. In patients with congenital heart disease, it is most frequently observed in single ventricular anatomies after Fontan palliation. The pathophysiology of plastic bronchitis remains unknown, and a consistently effective treatment strategy has yet to be identified. We report two cases of plastic bronchitis in patients with Fontan physiology. The first was treated with Fontan conversion and, despite encouraging short-term results, experienced recurrence of cast formation seven months postoperatively. The second underwent cardiac transplantation and has been free of bronchial casts for over one year. In addition, we explore the similarities between plastic bronchitis and protein-losing enteropathy, considering theories of their pathophysiologic mechanisms and reports of mutually effective treatment strategies. We propose that bronchial cast formation may result from the confluence of genetic makeup, inflammation, and the Fontan physiology and conclude that further investigation into therapies directed at these factors is merited.
塑料支气管炎是一种罕见的、危及生命的疾病,其特征是在肺支气管内形成黏液纤维蛋白铸型。在先天性心脏病患者中,最常发生于Fontan姑息治疗后的单心室解剖结构中。塑料支气管炎的病理生理学尚不清楚,且尚未确定一种始终有效的治疗策略。我们报告了两例Fontan生理状态患者的塑料支气管炎病例。第一例接受了Fontan转换术,尽管短期结果令人鼓舞,但术后7个月铸型形成复发。第二例接受了心脏移植,术后一年多未出现支气管铸型。此外,我们探讨了塑料支气管炎与蛋白丢失性肠病之间的相似性,考虑了它们病理生理机制的理论以及相互有效的治疗策略的报道。我们认为支气管铸型的形成可能是基因构成、炎症和Fontan生理状态共同作用的结果,并得出结论,值得对针对这些因素的治疗方法进行进一步研究。