PDF(Pubmed)
Abstract：
Idiopathic pulmonary hemosiderosis (IPH) is a rare and fatal lung disease. Mycoplasma pneumoniae pneumonia (MPP) is the main community-acquired pneumonia among children aged 5 and above in China. We report the following case of IPH complicated with severe mycoplasma pneumoniae pneumonia(SMPP). An 8-year-old boy with cough and fever was diagnosed with IPH for 3 years and his chest computed tomography showed bilateral bronchopneumonia, lobular consolidation and subpleural interstitial fibrosis. As far as we know, IPH related to SMPP is rarely reported. In the high incidence period of MPP, clinicians and radiologists should be alert to the co-occurrence of IPH and SMPP.
摘要：
特发性肺含铁血黄素沉着症（IPH）是一种罕见且致命的肺部疾病。肺炎支原体肺炎(MPP)是我国5岁及以上儿童主要的社区获得性肺炎。我们报告了以下IPH并发重症肺炎支原体肺炎（SMPP）的病例。一名咳嗽发烧的八岁男童被诊断为IPH3年,胸部CT显示双侧支气管肺炎,小叶实变和胸膜下间质纤维化。据我们所知,很少报道与SMPP相关的IPH。在MPP的高发期,临床医生和放射科医师应警惕IPH和SMPP的共存.
