阿奇霉素
肺表面活性物质
薄壁组织
医学
肺
肺病
内科学
病理
抗生素
化学
微生物学
生物
生物化学
作者
Guillaume Thouvenin,Nadia Nathan,Ralph Epaud,Annick Clément
出处
期刊:Case Reports
[BMJ]
日期:2013-06-24
卷期号:: bcr2013009988-bcr2013009988
被引量:52
标识
DOI:10.1136/bcr-2013-009988
摘要
Pulmonary surfactant deficiency caused by mutations in ABCA3 (ATP-binding cassette transporter of the A subfamily, member 3) gene results in diffuse parenchymal lung disease (DPLD) in children. So far, systemic steroids are the main treatment, with however limited efficacy. We report the case of a young boy showing a dramatic long-term improvement of respiratory disease by low-dose azithromycin (AZM) with no side effect after 6 years of treatment. Cellular and molecular studies are ongoing to progress in the understanding of the mechanisms involved. On behalf of the National Reference Center for rare lung diseases in France (Respirare, http://www.respirare.fr ), clinical studies on AZM in various forms of DPLD in children have been initiated and should provide information on the types of paediatric DPLD that may benefit from this treatment.
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