| Literature DB >> 19329018 |
Deniz Doğru1, Ebru Yalçin, Ayşe Tana Aslan, Turgay Ocal, Uğur Ozçelik, Safak Güçer, Gülsev Kale, Mithat Haliloglu, Nural Kiper.
Abstract
Pulmonary alveolar proteinosis (PAP) is a rare disorder in which lipoproteinaceous material accumulates within the alveoli. A 4-year-old child with autoimmune PAP, who was successfully treated with a series of unilateral partial bronchoalveolar lavages by selectively ventilating the other lung with a cuffed endotracheal tube, is presented.Entities:
Mesh：
Year: 2009 PMID： 19329018 DOI： 10.1016/j.jclinane.2008.06.035
Source DB: PubMed Journal: J Clin Anesth ISSN： 0952-8180 Impact factor: 9.452