| Literature DB >> 18618617 |
Hajime Yamamoto1, Etsuro Yamaguchi, Hiroatsu Agata, Nobuhisa Kandatsu, Toru Komatsu, Seiko Kawai, Kenji Baba, Tomonari Awaya, Ryuta Nishikomori, Masahito Tsurusawa, Koh Nakata.
Abstract
Systemic and inhalation therapy of granulocyte-macrophage colony-stimulating factor (GM-CSF) is usually effective in controlling autoimmune pulmonary alveolar proteinosis (PAP), but some cases are refractory to GM-CSF therapy and subjected to whole lung lavage (WLL). A 9-year-old girl developed severe respiratory failure due to autoimmune PAP was treated with inhalational 250 microg of GM-CSF daily, however, it was ineffective. Unilateral WLL was performed three times and subsequent GM-CSF inhalation therapy yielded marked physiological and radiological improvement and was continued for 1 year. (c) 2008 Wiley-Liss, Inc.Entities:
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Year: 2008 PMID: 18618617 DOI: 10.1002/ppul.20856
Source DB: PubMed Journal: Pediatr Pulmonol ISSN: 1099-0496