早产儿食管肺的多学科治疗报告

IF 0.6 Q4 SURGERY
E. Villamizar, Maria Daniela Moreno Villamizar, Mauricio Pedraza Ciro, Jean A. Pulido, Maria Rodriguez, Juan Carlos Villamizar
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引用次数: 3

摘要

摘要食管肺是一种罕见的实体,由前肠腹壁形成过程中的胚胎改变引起。这种病理的临床表现是模糊的,包括呼吸道或消化系统症状、重复性呼吸道感染、吞咽困难或无法吞咽。管理是基于确切的解剖和血管异常。我们报告了一例患有食道肺的早产儿的诊断和治疗方法。此外,我们还提出了一个三维模型来对这种病理进行分类。总之,管理依赖于解剖结构和手术策略的正确定义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Esophageal Lung in a Preterm Boy—Report on a Multidisciplinary Treatment
Abstract Esophageal lung is a rare entity that results from embryological alterations during the formation of the ventral wall of the anterior intestine. The clinical manifestations of this pathology are vague, including respiratory or digestive symptoms, repetitive respiratory infections, dysphagia, or inability to swallow. The management is based on the exact anatomical and vascular abnormalities. We report the diagnostic and therapeutic approach in a preterm boy with esophageal lung. Also, we present a three-dimensional model for the classification of this pathology. In conclusion, the management relies on proper definition of the anatomy and the surgical strategy.
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来源期刊
自引率
33.30%
发文量
39
审稿时长
12 weeks
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