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儿童塑料支气管炎:病例系列及医学文献综述

Plastic bronchitis in children: a case series and review of the medical literature.

作者信息

Brogan Thomas V, Finn Laura S, Pyskaty D James, Redding Gregory J, Ricker David, Inglis Andrew, Gibson Ronald L

机构信息

Children's Hospital and Regional Medical Center, Seattle, Washington 98105, USA.

出版信息

Pediatr Pulmonol. 2002 Dec;34(6):482-7. doi: 10.1002/ppul.10179.

Abstract

Plastic bronchitis is characterized by marked obstruction of the large airways by bronchial casts. We reviewed our experience and the literature to determine whether mortality rates are determined by underlying disease or cast type. We present 3 children with obstructive bronchial casts. One 3-year-old patient with Noonan's syndrome developed respiratory failure following surgery for tetralogy of Fallot requiring support with extracorporeal membrane oxygenation (ECMO) the first such case. There were 42 cases in the literature of children with plastic bronchitis. Casts may be divided into two types. Type I casts are inflammatory, consisting mainly of fibrin with cellular infiltrates, and occur in inflammatory diseases of the lung. Type II, or acellular casts, consist mainly of mucin with a few cells, and usually occur following surgery for congenital cardiac defects. Patients categorized by underlying disease included 31% with asthma or allergic disease, 40% with underlying cardiac defects, and 29% with other diseases. Mortality was 16%, but increased to 29% in patients with cardiac defects. Deaths occurred as long as 1 year after surgical repair for underlying defects. There were no deaths in patients with asthma. Life-threatening events were statistically higher in patients with cardiac defects (41%) than in those with asthma (0%, P = 0.02). Higher mortality in patients with type II casts compared to type I casts did not reach statistical significance (28% vs. 6%; P = 0.06). In conclusion, patients presenting with plastic bronchitis are at high risk for serious complications, especially with underlying cardiac disease.

摘要

塑料支气管炎的特征是支气管铸型导致大气道明显阻塞。我们回顾了我们的经验和文献,以确定死亡率是否由基础疾病或铸型类型决定。我们报告了3例患有阻塞性支气管铸型的儿童。一名3岁患有努南综合征的患者在法洛四联症手术后出现呼吸衰竭,需要体外膜肺氧合(ECMO)支持,这是首例此类病例。文献中报道了42例儿童塑料支气管炎病例。铸型可分为两种类型。I型铸型为炎性,主要由纤维蛋白和细胞浸润组成,见于肺部炎性疾病。II型或无细胞铸型主要由粘蛋白和少量细胞组成,通常发生在先天性心脏缺陷手术后。按基础疾病分类的患者中,31%患有哮喘或过敏性疾病,40%有基础心脏缺陷,29%患有其他疾病。死亡率为16%,但有心脏缺陷的患者死亡率增至29%。死亡发生在基础缺陷手术修复后长达1年的时间。哮喘患者无死亡病例。有心脏缺陷的患者发生危及生命事件的比例(41%)在统计学上高于哮喘患者(0%,P = 0.02)。II型铸型患者与I型铸型患者相比死亡率更高,但未达到统计学显著性(28%对6%;P = 0.06)。总之,患有塑料支气管炎的患者发生严重并发症的风险很高,尤其是有基础心脏疾病的患者。

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