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Rare combination of congenital heart disease and pulmonary alveolar proteinosis
被引:1
|作者:
Tanaka, Yuki
[1
]
Miyamoto, Takashi
[1
]
Yoshitake, Shuichi
[1
]
Naito, Yuji
[1
]
Kobayashi, Tomio
[2
]
机构:
[1] Gunma Childrens Med Ctr, Dept Pediat Cardiovasc Surg, Shibukawa, Gunma 3778577, Japan
[2] Gunma Childrens Med Ctr, Pediat Cardiol, Shibukawa, Gunma 3778577, Japan
关键词:
congenital heart disease;
lung disease;
neonate;
pulmonary alveolar proteinosis;
total anomalous pulmonary venous return;
D O I:
10.1111/ped.12695
中图分类号:
R72 [儿科学];
学科分类号:
100202 ;
摘要:
Here, we describe a case of total anomalous pulmonary venous return with coarctation of the aorta that was diagnosed as pulmonary alveolar proteinosis at autopsy in a male infant. Surgical repair was performed at 1day of age, but the infant died on postoperative day 51 due to respiratory insufficiency without any evidence of pulmonary venous obstruction. He had been unexpectedly diagnosed with pulmonary alveolar proteinosis and pulmonary hypoplasia on autopsy. Congenital pulmonary alveolar proteinosis is a serious condition with a high mortality rate, which should be considered in the differential diagnosis in patients with a clinical picture of pulmonary venous obstruction, because most patients are unable to survive without proper treatment. In this report, we address specific issues that should be discussed in such cases based on our recent experience.
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页码:999 / 1001
页数:3
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