Doğru Deniz, Yalçin Ebru, Aslan Ayşe Tana, Ocal Turgay, Ozçelik Uğur, Güçer Safak, Kale Gülsev, Haliloglu Mithat, Kiper Nural
Pulmonary Medicine Unit, Department of Pediatrics, Hacettepe University, Sihhiye, Ankara, Turkey.
J Clin Anesth. 2009 Mar;21(2):127-30. doi: 10.1016/j.jclinane.2008.06.035.
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.
肺泡蛋白沉积症(PAP)是一种罕见的疾病,其中脂蛋白样物质在肺泡内积聚。本文介绍了一名患有自身免疫性PAP的4岁儿童,通过使用带套囊的气管内导管选择性地对另一侧肺进行通气,成功地接受了一系列单侧部分支气管肺泡灌洗治疗。