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获得性肺叶气肿(过度充气):需要进行肺叶切除术的婴儿的临床及病理评估

Acquired lobar emphysema (overinflation): clinical and pathological evaluation of infants requiring lobectomy.

作者信息

Azizkhan R G, Grimmer D L, Askin F B, Lacey S R, Merten D F, Wood R E

机构信息

Department of Surgery, University of North Carolina School of Medicine, Chapel Hill 27599.

出版信息

J Pediatr Surg. 1992 Aug;27(8):1145-51; discussion 1151-2. doi: 10.1016/0022-3468(92)90577-t.

Abstract

Acquired lobar "emphysema" (overinflation) (ALE) is an increasingly recognized complication of advanced bronchopulmonary dysplasia (BPD). To refine current concepts regarding patient management and pathogenesis, we examined clinical and pathological features of six infants with ALE who did not have obstructing intraluminal lesions and who underwent lobectomy after failing nonoperative management. All had severe neonatal respiratory distress and required prolonged ventilatory support (average, 2 months) with peak inspiratory pressures greater than 30 mm Hg and 100% oxygen. ALE developed between 3 weeks and 20 months of age (median, 5 months), with lobar hyperinflation, atelectasis, and mediastinal shift. Selective bronchial intubation provided only transient benefit. Videobronchoscopy demonstrated no intraluminal obstructing lesions in five patients. In one child, ALE became clinically apparent only after laser excision of an endobronchial cicatrix. All infants had bronchomalacia with the involved lobar bronchus being most severely affected. Ventilation-perfusion scans demonstrated severe impairment of both ventilation and perfusion in the involved lobes. The decision to perform lobectomy was based on clinical parameters and failure of non-operative management. After lobectomy, all children dramatically improved. However, only three of six were alive 2 to 3 years later; one infant died of unrelated causes at 6 weeks; and two died of progressive respiratory insufficiency 13 and 24 months postlobectomy. Microscopic evaluation of the lung demonstrated findings of late-stage BPD with peribronchial and interstitial fibrosis, parenchymal overinflation, and alveolar septal disruption.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

获得性肺叶“气肿”(过度充气)(ALE)是晚期支气管肺发育不良(BPD)一种越来越被认识到的并发症。为了完善当前关于患者管理和发病机制的概念,我们检查了6例ALE婴儿的临床和病理特征,这些婴儿没有腔内阻塞性病变,在非手术治疗失败后接受了肺叶切除术。所有患儿均有严重的新生儿呼吸窘迫,需要长时间通气支持(平均2个月),吸气峰压大于30 mmHg,吸氧浓度100%。ALE在3周龄至20个月龄(中位数5个月)之间出现,伴有肺叶过度充气、肺不张和纵隔移位。选择性支气管插管仅提供短暂益处。电子支气管镜检查显示5例患者无腔内阻塞性病变。在1例患儿中,ALE仅在激光切除支气管内瘢痕后才在临床上显现。所有婴儿均有支气管软化,受累肺叶支气管受影响最严重。通气-灌注扫描显示受累肺叶通气和灌注均严重受损。决定行肺叶切除术基于临床参数和非手术治疗失败。肺叶切除术后,所有患儿均显著改善。然而,6例中只有3例在2至3年后存活;1例婴儿在6周时死于无关原因;2例在肺叶切除术后13个月和24个月死于进行性呼吸功能不全。肺组织显微镜检查显示为晚期BPD的表现,伴有支气管周围和间质纤维化、实质过度充气和肺泡间隔破坏。(摘要截短至250字)

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