Pulmonary hypoplasia with associated cardiac and skeletal malformations.

Q4 Medicine
Pneumologia Pub Date : 2015-01-01
Efrén Martínez-Quintana, Fayna Rodríguez-González
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引用次数: 0

Abstract

Patients with mild pulmonary hypoplasia typically use to have minimal respiratory symptoms. Nonetheless, other associated anomalies such as cardiac, gastrointestinal, genitourinary, or skeletal defects may be seen. We report the case of a 17-year-old male patient with hypoplastic right lung with secondary cardiac dextroposition, an ostium secundum atrial septal defect, a hypoplastic right pulmonary artery arising from the posterior wall of the left pulmonary artery with a retrocava course, vertebral bone fusion and pollicization due to right congenital thumb absence.

肺发育不全伴心脏和骨骼畸形。
轻度肺发育不全的患者通常有最小的呼吸道症状。尽管如此,其他相关的异常,如心脏、胃肠道、泌尿生殖系统或骨骼缺陷也可能出现。我们报告一例17岁男性右肺发育不全伴继发性心脏右位,第二口房间隔缺损,右肺动脉发育不全起源于左肺动脉后壁伴腔后走行,椎体骨融合及右拇指缺失所致极化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pneumologia
Pneumologia Medicine-Pulmonary and Respiratory Medicine
CiteScore
0.20
自引率
0.00%
发文量
10
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