| Literature DB >> 27435178 |
Tsubasa Aiyoshi1, Kouji Masumoto1, Toko Shinkai2, Yasunari Tanaka1, Shunsuke Fujii1, Takato Sasaki1, Fumiko Chiba1, Naoya Sakamoto1, Chikashi Gotoh1, Yasuhisa Urita1, Makoto Nakao1, Hajime Takayasu1, Hideaki Tanaka1, Hironori Imai3.
Abstract
Pulmonary interstitial emphysema (PIE) primarily affects premature infants on positive pressure ventilation. PIE is rarely reported in infants and children in the absence of mechanical ventilation and/or associated respiratory infection. We report a case of PIE in a 22-month-old girl who had severe respiratory distress due to respiratory syncytial virus infection. Chest computed tomography showed cystic lung lesions mimicking congenital cystic adenomatoid malformation. The cystic lesions spontaneously resolved after conservative treatment. Based on the clinical course and the chronological changes on imaging, the cystic lung lesions were diagnosed as localized persistent PIE.Entities:
Keywords: congenital cystic adenomatoid malformation; mechanical ventilation; pulmonary interstitial emphysema; respiratory syncytial virus
Mesh:
Year: 2016 PMID: 27435178 DOI: 10.1111/ped.13013
Source DB: PubMed Journal: Pediatr Int ISSN: 1328-8067 Impact factor: 1.524