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A Rare Case of Aortic Coarctation and Ventricular Septal Defect Combined with Alveolar Capillary Dysplasia

机译:少见的主动脉缩窄和室间隔缺损合并肺泡毛细血管发育不良的病例

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摘要

We report a rare case of alveolar capillary dysplasia (ACD) associated with severe aortic coarctation, hypoplastic aortic arch, and mild hypoplasia of the left ventricle. After successful coarctation repair, pulmonary hypertension persisted, and despite only minor anomalies on the x-ray, chest computed tomography (CT) revealed the presence of primary lung disease. Review of the literature suggests that ACD may be associated with left heart obstructions. Chest CT is applicable to diagnose ACD precociously.
机译:我们报告少见的肺泡毛细血管发育不良(ACD)与严重的主动脉缩窄,增生的主动脉弓和左心室轻度增生相关。成功的缩窄修复后,肺动脉高压仍然存在,尽管X线检查仅出现少量异常,胸部计算机断层扫描(CT)仍显示出原发性肺部疾病。文献回顾表明,ACD可能与左心梗阻有关。胸部CT适用于早诊断ACD。

著录项

  • 来源
    《Pediatric Cardiology》 |2007年第4期|319-323|共5页
  • 作者单位

    Department of Congenital Heart Disease University of Freiburg Mathildenstrasse 1 D-79106 Freiburg Germany;

    Department of Congenital Heart Disease University of Freiburg Mathildenstrasse 1 D-79106 Freiburg Germany;

    Department of Pathology University of Freiburg Mathildenstrasse 1 D-79106 Freiburg Germany;

    Department of Congenital Heart Disease University of Freiburg Mathildenstrasse 1 D-79106 Freiburg Germany;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Alveolar capillary dysplasia; Congenital heart disease; Chest computed tomography;

    机译:肺泡毛细血管发育不良;先天性心脏病;胸部计算机断层扫描;

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