Reexpansion Pulmonary Edema following Tube Thoracostomy in a Pediatric Patient with Anterior Mediastinal Mass

Q3 Medicine Case Reports in Anesthesiology Pub Date : 2022-05-19 DOI:10.1155/2022/8547611
S. Choi, Deborah A. Romeo, David A Gutman, Jennifer V. Smith
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引用次数: 1

Abstract

Reexpansion pulmonary edema (RPE) is an exceedingly rare and potentially fatal complication of a rapidly reexpanded lung following evacuation of air or fluid from the pleural space secondary to conditions such as a mediastinal mass, pleural effusion, or pneumothorax. Clinical presentations can range from mild radiographic changes to acute respiratory failure and hemodynamic instability. The rapidly progressive nature of the disease makes it important for clinicians to appropriately diagnose and manage patients who develop RPE. We present a case of a child with a large malignant pleural effusion who developed severe RPE after tube thoracostomy and ultimately required venoarterial extracorporeal membrane oxygenation (VA-ECMO). The patient was 7-year-old Caucasian male with newly diagnosed ambiguous T cell myeloid leukemia. A chest computerized tomography (CT) demonstrated a large pleural effusion causing tracheal shift and left bronchus compression as well as an anterior mediastinal mass causing compression of the right atria and right ventricle. Tube thoracostomy was performed in the operating room (OR) with deep sedation. The procedure was complicated with hypoxemia, bradycardia, and pulseless cardiac arrest. After return of spontaneous circulation, the child continued to have refractory hypoxemia, profound hypotension, and frothy secretions. Endotracheal intubation was performed with a size 5.0 cuffed endotracheal tube. Chest radiograph demonstrated opacification of the left hemithorax with chest infiltrates. Patient required VA-ECMO for circulatory support. Supportive therapy of RPE was continued and decannulation was done on day three. Tracheal extubation was performed on day five.
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小儿前纵隔肿块插管造胸术后再扩张肺水肿一例
再扩张性肺水肿(RPE)是一种极为罕见且具有潜在致命性的并发症,它是由纵隔肿块、胸腔积液或气胸等继发于胸膜间隙的空气或液体排出后肺迅速再扩张所致。临床表现可以从轻微的x线改变到急性呼吸衰竭和血流动力学不稳定。这种疾病的快速进展性质使得临床医生对发展为RPE的患者进行适当的诊断和管理变得非常重要。我们报告了一个患有大量恶性胸腔积液的儿童,他在插管开胸术后发生了严重的RPE,最终需要静脉体外膜氧合(VA-ECMO)。患者为7岁白人男性,新诊断为模棱两可的T细胞髓性白血病。胸部计算机断层扫描(CT)显示大量胸腔积液导致气管移位和左支气管受压,以及前纵隔肿块导致右心房和右心室受压。在深度镇静的情况下,在手术室进行插管开胸术。手术过程很复杂,伴有低氧血症、心动过缓和无脉性心脏骤停。自然循环恢复后,患儿继续出现难治性低氧血症、深度低血压和泡沫性分泌物。气管插管采用5.0号套管气管插管。胸片示左半胸混浊伴胸部浸润。患者需要VA-ECMO进行循环支持。继续RPE的支持治疗,并于第3天进行脱管。第5天进行气管拔管。
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来源期刊
Case Reports in Anesthesiology
Case Reports in Anesthesiology Medicine-Anesthesiology and Pain Medicine
CiteScore
1.40
自引率
0.00%
发文量
19
审稿时长
12 weeks
期刊最新文献
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