Yanagihara Toyoshi, Yamamoto Yuzo, Hamada Naoki, Suzuki Kunihiro, Ogata-Suetsugu Saiko, Harada Eiji, Tagawa Tetsuzo, Fujiwara Minako, Hashisako Mikiko, Fukuoka Junya, Nakanishi Yoichi
Research Institute for Diseases of the Chest, Graduate School of Medical Sciences, Kyushu University, Japan.
Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Japan.
Respir Med Case Rep. 2018 Jun 30;25:68-72. doi: 10.1016/j.rmcr.2018.06.013. eCollection 2018.
We report a case of recurrent idiopathic pulmonary hemosiderosis after a long-term remission presented with Sjögren's syndrome. The patient was diagnosed with IPH due to repeated pneumonia and blood sputum in his childhood. He was admitted to our hospital due to exertional dyspnea and dry cough with bilateral ground-glass opacity in chest computed tomography at the age of 32. Video-assisted thoracoscopic surgery was performed and the specimens showed nonspecific interstitial pneumonia pattern with diffuse, chronic alveolar hemorrhage, suggesting recurrence of IPH. He was also diagnosed with Sjögren's syndrome. Further immunological studies will reveal the pathogenesis of IPH.
我们报告一例长期缓解后复发的特发性肺含铁血黄素沉着症,该患者同时患有干燥综合征。该患者童年时因反复肺炎和咯血被诊断为特发性肺含铁血黄素沉着症。32岁时因劳力性呼吸困难和干咳入院,胸部计算机断层扫描显示双侧磨玻璃影。行电视辅助胸腔镜手术,标本显示为非特异性间质性肺炎模式伴弥漫性慢性肺泡出血,提示特发性肺含铁血黄素沉着症复发。他还被诊断为干燥综合征。进一步的免疫学研究将揭示特发性肺含铁血黄素沉着症的发病机制。