{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,10,2]],"date-time":"2023-10-02T07:18:55Z","timestamp":1696231135069},"reference-count":6,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2015,8,26]],"date-time":"2015-08-26T00:00:00Z","timestamp":1440547200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pediatrics International"],"published-print":{"date-parts":[[2015,10]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>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 1\u2009day 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.<\/jats:p>","DOI":"10.1111\/ped.12695","type":"journal-article","created":{"date-parts":[[2015,8,27]],"date-time":"2015-08-27T02:42:20Z","timestamp":1440643340000},"page":"999-1001","source":"Crossref","is-referenced-by-count":1,"title":["Rare combination of congenital heart disease and pulmonary alveolar proteinosis"],"prefix":"10.1111","volume":"57","author":[{"given":"Yuki","family":"Tanaka","sequence":"first","affiliation":[{"name":"Department of Pediatric Cardiovascular Surgery Gunma Children's Medical Center  Shibukawa Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Takashi","family":"Miyamoto","sequence":"additional","affiliation":[{"name":"Department of Pediatric Cardiovascular Surgery Gunma Children's Medical Center  Shibukawa Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shuichi","family":"Yoshitake","sequence":"additional","affiliation":[{"name":"Department of Pediatric Cardiovascular Surgery Gunma Children's Medical Center  Shibukawa Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yuji","family":"Naito","sequence":"additional","affiliation":[{"name":"Department of Pediatric Cardiovascular Surgery Gunma Children's Medical Center  Shibukawa Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tomio","family":"Kobayashi","sequence":"additional","affiliation":[{"name":"Pediatric Cardiology Gunma Children's Medical Center  Shibukawa Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2015,8,26]]},"reference":[{"key":"e_1_2_4_2_1","doi-asserted-by":"publisher","DOI":"10.1056\/NEJM195806052582301"},{"key":"e_1_2_4_3_1","first-page":"75","article-title":"Pulmonary alveolar proteinosis in Israel: Ethnic clustering","volume":"1","author":"Ben\u2010Dov I","year":"1999","journal-title":"Isr. 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